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Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Simple Summary: Many species of insects that infest stored products have developed a resistance to phosphine as a result of its widespread use to control stored-product pests. There is a significant opportunity for the development of natural fumigants as eco-friendly methods for controlling pests in stored products. A plant-derived molecule called methyl benzoate (MBe) is an example of a volatile organic compound that has potent insecticidal and fumigation toxicity. In this research, we examined its potential efficacy as a fumigation agent against phosphine-resistant strains of the lesser grain borer and rice weevil. Phosphine (PH3) has been widely used as a fumigant in food storage, but increasing PH3 resistance in major pests makes finding alternative fumigants urgent. Methyl benzoate (MBe), a volatile organic compound regarded to be a food-safe natural product, has recently demonstrated significant toxicity against a variety of insect pests. This study is the first evaluation of the fumigation toxicity of three benzoate compounds, MBe, vinyl benzoate, and ethyl benzoate, against PH3-susceptible and PH3-resistant strains of Rhyzopertha dominica and Sitophilus oryzae. All strains were exposed to the compounds at concentrations up to 20 µL/1.5 L air for 24 h. Compared to vinyl benzoate and ethyl benzoate, MBe induced higher mortality rates in all strains at all concentrations. When food was made available, the lethal median concentration for MBe was 10–17-fold higher than when tested without food. Moreover, no significant differences were observed between the responses of the PH3-susceptible and PH3-resistant strains to the compounds. Notably, S. oryzae was more susceptible to MBe. In laboratory settings, MBe successfully controlled PH3-resistant strains of R. dominica and S. oryzae, making it a viable option for PH3-resistance management. Thus, MBe might be suitable for food security programs as an environmentally benign alternative fumigant. [ABSTRACT FROM AUTHOR]

The impact of aluminum trialkyl (AlR3) and esters/silane-external electron donor (EED) on the activity and reaction kinetics of ZN catalyst (TiC14//MgCl2—ethyl benzoate/diisobutyl phthalate) in propylene polymerization was studied. The polymerization kinetic was studied for different types of catalysts with various types of EEDs. To correlate the kinetic behavior of propylene polymerization and various reactions taking place during the polymerization, we have studied in situ interactions of EEDs with co-catalyst by FT-NMR. The used EEDs are (1) p-isopropoxy methyl benzoate (PIPMB), (2) diphenyldimethoxy silane (DPDMS) and (3) mixture of isopropyl myristate (IPM) and (DPDMS) were interacted with triethyl aluminum (TEAl) at defined molar ratios. In the diester type of catalyst, two types of kinetic profile were observed with two different types of EED systems. Initially very fast polymerization kinetic was observed when only silane type of EED was used during polymerization which became steady with mixed EED (Silane + Aliphatic Ester). This EED system shows steady-state and controllable kinetic characteristics due to mixing of IPM with silane. The study by FT-NMR spectroscopy indicated the formation of the new compounds that are inhibiting the rate of polymerization reaction. The compounds, such as ketones and alcohols, are responsible for controlling the rate of polymerization reaction. The contribution of each of these product formations during processes depends on the catalyst composition and on the polymerization conditions. [ABSTRACT FROM AUTHOR]

Olfaction is critical for guiding the physiological activities of insects, with antennae being the primary olfactory organs. However, recent evidence suggests that other tissues may also participate in olfactory recognition. Among these, the genitalia of moths have received attention due to their roles in mating and oviposition. Sensilla and odorant receptors (ORs) in moth genitalia highlight the potential olfactory function of these structures. In this study, we examined the olfactory sensing capacity of the genitalia in Helicoverpa armigera by analyzing their structure in males and females and characterizing the expressed ORs. Scanning electron microscopy uncovered many sensilla distributed throughout the male and female genitalia. Transcriptome sequencing identified 20 ORs in the genitalia, with HarmOR68 exhibiting significant responses to methyl esters: methyl benzoate and salicylate. Our findings provide theoretical evidence that H. armigera genitalia may have significant olfactory perception functions. [ABSTRACT FROM AUTHOR]

It has been a quarter century since salicylic acid methyltransferase, the founding member of the plant SABATH enzyme family, was discovered. From making methyl benzoate to synthesizing caffeine, from modulating auxins and gibberellins to participating in strigolactone biosynthesis, new biochemical functions of SABATH methyltransferases have continuously been revealed, with more than 20 substrates of diverse structures identified. Three-dimensional structures for several members of the SABATH family have been solved, rendering explanations of reaction mechanism and structural basis of substrate specificity. The biological functions of several SABATH genes from diverse plants were elucidated by analyzing transgenic plants with overexpression, reduced expression or knock-out mutants of respective SABATH genes. In the majority of sequenced plants examined, SABATH genes constitute a medium-sized family. Diverse catalytic functions of SABATHs have evolved largely via gene duplication followed by functional divergence. Some SABATH family members have a deep evolutionary origin; some others, while catalyzing an identical reaction, evolved more than once. Equally important, many members acquired lineage-specific functions. All these are indicative of the important contributions of the SABATH family to land plant evolution and adaptation. [ABSTRACT FROM AUTHOR]

Copyright of Scientific Journal of Agricultural Sciences (SJAS) is the property of Beni Suef University and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Tunable‐lifetime room‐temperature phosphorescence (RTP) materials have been widely studied due to their broad applications. However, only few reports have achieved wide‐range lifetime modulation. In this work, ultra‐wide range tunable‐lifetime efficient dark blue RTP materials were realized by doping methyl benzoate derivatives into polyvinyl alcohol (PVA) matrix. The phosphorescence lifetimes of the doped films can be increased from 32.8 ms to 1925.8 ms. Such wide range of phosphorescence lifetime modulation is extremely rare in current reports. Moreover, the phosphorescence emission of the methyl 4‐hydroxybenzoate‐doped film is located in the dark blue region and the phosphorescence quantum yield reaches as high as 15.4 %, which broadens their applications in organic optoelectronic information. Further studies demonstrated that the reason for the tunable lifetime was that the magnitude of the electron‐donating ability of the substituent group modulates the HOMO–LUMO and singlet‐triplet energy gap of methyl benzoate derivatives, as well as the ability to non‐covalent interactions with PVA. Moreover, the potential applications of luminescent displays and optical anti‐counterfeiting of these high‐performance dark blue RTP materials have been conducted. [ABSTRACT FROM AUTHOR]

Tunable‐lifetime room‐temperature phosphorescence (RTP) materials have been widely studied due to their broad applications. However, only few reports have achieved wide‐range lifetime modulation. In this work, ultra‐wide range tunable‐lifetime efficient dark blue RTP materials were realized by doping methyl benzoate derivatives into polyvinyl alcohol (PVA) matrix. The phosphorescence lifetimes of the doped films can be increased from 32.8 ms to 1925.8 ms. Such wide range of phosphorescence lifetime modulation is extremely rare in current reports. Moreover, the phosphorescence emission of the methyl 4‐hydroxybenzoate‐doped film is located in the dark blue region and the phosphorescence quantum yield reaches as high as 15.4 %, which broadens their applications in organic optoelectronic information. Further studies demonstrated that the reason for the tunable lifetime was that the magnitude of the electron‐donating ability of the substituent group modulates the HOMO–LUMO and singlet‐triplet energy gap of methyl benzoate derivatives, as well as the ability to non‐covalent interactions with PVA. Moreover, the potential applications of luminescent displays and optical anti‐counterfeiting of these high‐performance dark blue RTP materials have been conducted. [ABSTRACT FROM AUTHOR]

Copyright of China Surfactant Detergent & Cosmetics (2097-2806) is the property of China Surfactant Detergent & Cosmetics Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

A series of potasium boasted phosphomolybdic acid (PM) catalysts were successfully synthesized by ion-exchange method. These materials were characterized by BET surface area, FT-IR, XRD, Pyridine adsorbed FT-IR and TEM analysis to find the structural and nature of acidic sites of the catalyst. BET surface area result reveals that surface area significantly improved after K loadings compare to pure phosphomolybdic acid. XRD results provide crystallites of cubic Keggin ion were observed after K loading. FT-IR results provide characteristic Keggin ion bands were retained even after K loadings. TEM analysis reveals spherical morphology is maintained even after K loadings and KPM-2 catalyst exhibits smaller particle size than other K loadings. Pyridine adsorbed FT-IR spectra exhibits Brønsted to Lewis acidic sites ratio is higher in case of KPM-2 when compared to other K loadings. These synthesized K boasted PM materials were evaluated for oxidative esterification of benzyl alcohol to methyl benzoate possesses higher activity and selectivity during reaction than pure PM catalyst. [ABSTRACT FROM AUTHOR]

Upgrading of polyethylene terephthalate (PET) waste into valuable oxygenated molecules is a fascinating process, yet it remains challenging. Herein, we developed a two‐step strategy involving methanolysis of PET to dimethyl terephthalate (DMT), followed by hydrogenation of DMT to produce the high‐valued chemical methyl p‐methyl benzoate (MMB) using a fixed‐bed reactor and a Cu/ZrO2 catalyst. Interestingly, we discovered the phase structure of ZrO2 significantly regulates the selectivity of products. Cu supported on monoclinic ZrO2 (5 %Cu/m‐ZrO2) exhibits an exceptional selectivity of 86 % for conversion of DMT to MMB, while Cu supported on tetragonal ZrO2 (5 %Cu/t‐ZrO2) predominantly produces p‐xylene (PX) with selectivity of 75 %. The superior selectivity of MMB over Cu/m‐ZrO2 can be attributed to the weaker acid sites present on m‐ZrO2 compared to t‐ZrO2. This weak acidity of m‐ZrO2 leads to a moderate adsorption capability of MMB, and facilitating its desorption. Furthermore, DFT calculations reveal Cu/m‐ZrO2 catalyst shows a higher effective energy barrier for cleavage of second C−O bond compared to Cu/t‐ZrO2 catalyst; this distinction ensures the high selectivity of MMB. This catalyst not only presents an approach for upgrading of PET waste into fine chemicals but also offers a strategy for controlling the primary product in a multistep hydrogenation reaction. [ABSTRACT FROM AUTHOR]

Upgrading of polyethylene terephthalate (PET) waste into valuable oxygenated molecules is a fascinating process, yet it remains challenging. Herein, we developed a two‐step strategy involving methanolysis of PET to dimethyl terephthalate (DMT), followed by hydrogenation of DMT to produce the high‐valued chemical methyl p‐methyl benzoate (MMB) using a fixed‐bed reactor and a Cu/ZrO2 catalyst. Interestingly, we discovered the phase structure of ZrO2 significantly regulates the selectivity of products. Cu supported on monoclinic ZrO2 (5 %Cu/m‐ZrO2) exhibits an exceptional selectivity of 86 % for conversion of DMT to MMB, while Cu supported on tetragonal ZrO2 (5 %Cu/t‐ZrO2) predominantly produces p‐xylene (PX) with selectivity of 75 %. The superior selectivity of MMB over Cu/m‐ZrO2 can be attributed to the weaker acid sites present on m‐ZrO2 compared to t‐ZrO2. This weak acidity of m‐ZrO2 leads to a moderate adsorption capability of MMB, and facilitating its desorption. Furthermore, DFT calculations reveal Cu/m‐ZrO2 catalyst shows a higher effective energy barrier for cleavage of second C−O bond compared to Cu/t‐ZrO2 catalyst; this distinction ensures the high selectivity of MMB. This catalyst not only presents an approach for upgrading of PET waste into fine chemicals but also offers a strategy for controlling the primary product in a multistep hydrogenation reaction. [ABSTRACT FROM AUTHOR]

In this study, benzohydroxamic acid molecules were synthesized from methyl 4‐amino‐2‐methoxy, methyl 4‐amino‐3‐nitro, methyl 4‐amino‐3‐methyl, and methyl 4‐amino‐3‐chloro benzoate molecules, and the horseradish peroxidase (HRP) enzyme was purified in one step using the affinity chromatography technique for the first time. The IC50 and Ki values for the 4‐amino 3‐methyl benzohydroxamic acid molecule were 0.136 and 0.132 ± 0.054 μM, respectively, while the IC50 and Ki values for the 4‐amino‐3‐nitro benzohydroxamic acid molecule were 56.00 and 51.90 ± 9.90 μM, respectively. It was found that the IC50 and Ki values for the 4‐amino‐3‐chloro benzohydroxamic acid molecule were 218.33 and 175.67 ± 43.78 μM, respectively, whereas the IC50 and Ki values for the 4‐amino‐2‐methoxy benzohydroxamic acid molecule were 306.00 and 218.00 ± 68.80 μM, respectively. The HRP enzyme was synthesized from 4‐amino‐2‐methoxy hydroxamic acid column with a 35.97% yield 601.13 times, 4‐amino‐3‐nitro hydroxamic acid column, with a 14.00% yield 404.11 times, 4‐amino‐3‐methyl hydroxamic acid column with an 8.70% yield 394.88 times, and 4‐amino‐3‐chloro hydroxamic acid column with a 4.48% yield 284.85 times. Thus, the HRP enzyme was purified in a single step with hydroxamic acids, and its molecular weight was found to be 44 kDa. The optimum pH was 8.0, the optimum temperature was 15°C, and the optimum ionic strength was 0.4 M for the purified HRP enzyme. [ABSTRACT FROM AUTHOR]

The crystal structures and Hirshfeld surface analyses of three similar azo compounds are reported. Methyl 4-{2,2-di­chloro-1-[(E)-phenyl­diazen­yl]ethen­yl}benzoate, C16H12Cl2N2O2, (I), and methyl 4-{2,2-di­chloro-1-[(E)-(4-methyl­phen­yl)diazen­yl]ethen­yl}benzoate, C17H14Cl2N2O2, (II), crystallize in the space group P21/c with Z = 4, and methyl 4-{2,2-di­chloro-1-[(E)-(3,4-di­methyl­phen­yl)diazen­yl]ethen­yl}benzoate, C18H16Cl2N2O2, (III), in the space group P with Z = 2. In the crystal of (I), mol­ecules are linked by C--H...N hydrogen bonds, forming chains with C(6) motifs parallel to the b axis. Short inter­molecular Cl...O contacts of 2.8421(16)Å and weak van der Waals inter­actions between these chains stabilize the crystal structure. In (II), mol­ecules are linked by C--H...O hydrogen bonds and C--Cl...π inter­actions, forming layers parallel to (010). Weak van der Waals inter­actions between these layers consolidate the mol­ecular packing. In (III), mol­ecules are linked by C--H...π and C--Cl...π inter­actions forming chains parallel to [011]. Furthermore, these chains are connected by C--Cl...π inter­actions parallel to the a axis, forming (0 1) layers. The stability of the mol­ecular packing is ensured by van der Waals forces between these layers. [ABSTRACT FROM AUTHOR]

Anisandrus maiche Stark (Coleoptera: Curculionidae: Scolytinae) is a non-native ambrosia beetle from central Asia that has been spreading throughout the eastern United States since 2005. Preferred hosts of A. maiche are not well characterized within its currently invaded range, but it is established in managed and natural forests throughout Indiana. Current monitoring and detection efforts for this beetle rely on ethanol-baited traps, but fungal volatiles may alter the attraction of A. maiche to ethanol. In this study, we conducted trapping experiments in Indiana to determine the extent to which a suite of common fungal alcohols influences the response of A. maiche to ethanol-baited traps. We then evaluated isoamyl and isobutyl alcohol as potential attractants for A. maiche and their ability to enhance attraction to ethanol. Lastly, we used SPME-GC-MS to identify volatiles from Ambrosiella cleistominuta (Mayers & Harr.), the fungal symbiont of A. maiche , grown for 7 and 14 days on malt extract agar. Benzyl alcohol, isobutyl alcohol, hexanol, methyl phenylacetate, phenethyl alcohol, and piperitone reduced the attraction of A. maiche to ethanol-baited traps in the field. Moreover, adding methyl benzoate and isoamyl alcohol individually to ethanol-baited traps did not further increase A. maiche capture. When paired with ethanol, isoamyl alcohol repelled beetles in the early flight period but did not significantly increase trap capture during the fall flight. These results represent a first step in understanding the role of fungal volatiles in the colonization behavior of A. maiche and may ultimately inform management strategies for this species. [ABSTRACT FROM AUTHOR]

Simple Summary: The spotted-wing drosophila (SWD), Drosophila suzukii, is an invasive pest of soft-skinned fruits that has rapidly spread across the globe and causes hundreds of millions of dollars in crop losses worldwide. Today, the management of SWD heavily relies on the application of synthetic pesticides, which are potentially hazardous to humans, animals, other organisms, and the environment. A natural-product-based sustainable integrated pest management approach is urgently needed to reduce conventional synthetic pesticide usages. A promising behavior-based control method is the "push–pull" strategy, which uses a repellent to drive pests away from fruits (push) and towards SWD attractant-baited mass trapping devices (pull). Methyl benzoate, a naturally occurring chemical found in many plants and FDA-approved food additives, was found to be repellent to SWD in laboratory tests. In this study, we tested whether this compound could also be used to protect blueberries from SWD injury in the field. Our results demonstrated that methyl benzoate as a spatial repellent/oviposition deterrent can be deployed in blueberry fields to reduce the damage caused by SWD, although this repellent is not sufficient to act as a control strategy alone and will need to be integrated with other strategies to provide adequate protection to growers. We evaluated a novel push–pull control strategy for protecting highbush blueberry, Vaccinium corymbosum, against spotted-wing drosophila (SWD), Drosophila suzukii. Methyl benzoate (MB) was used as the pushing agent and a previously tested SWD attractive blend of lure-scents was used as the pulling agent. MB dispensers (push) were hung in the canopy and lure-scent dispensers (pull) were hung in yellow jacket traps filled with soapy water around the blueberry bushes. Blueberries were sampled weekly, and any infestation was inspected by examining the breathing tubes of SWD eggs which protrude through the skin of infested fruit. The frequency of infestation, i.e., the proportion of berries infested with at least one egg, and the extent of infestation, i.e., the mean number of eggs in infested berries, were significantly reduced in treatments receiving MB dispensers as a pushing agent when infestation rates were very high. However, the mass trapping devices as a pulling agent did not provide comparable protection on their own and did not produce additive protection when used in combination with the MB dispensers in push–pull trials. We conclude that MB has the potential to be implemented as a spatial repellent/oviposition deterrent to reduce SWD damage in blueberry under field conditions and does not require the SWD attractant as a pulling agent to achieve crop protection. [ABSTRACT FROM AUTHOR]

The synthesis of benzaldehyde, a compound widely utilized in food, medicine, and cosmetics, was achieved through a one-step catalytic hydrogenation using the cost-effective raw material, methyl benzoate. This process aligns with the principles of atom economy and green production. Despite the development of numerous high-performance catalysts by scholars, the challenge remains in achieving lower reaction temperatures, ideally below 400 °C. In this study, a series of MnOx/γ-Al2O3 catalysts were meticulously prepared using the precipitation-impregnation method. These catalysts featured supports calcined at various temperatures and distinct manganese active components. Characterization techniques such as X-ray diffraction (XRD), N2 physical adsorption, Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), H2 temperature programmed reduction (H2-TPR), and NH3 temperature-programmed desorption (NH3-TPD) were employed to analyze the structure and surface properties of the catalysts. Notably, the optimized reaction temperature was found to be 360 °C. The catalyst exhibited the most favorable performance when the calcination temperature of the support was 500 °C and the Mn/Al molar ratio reached 0.18. Under these conditions, the catalyst demonstrated the most suitable oxygen vacancy concentration, yielding impressive results: a conversion rate of 87.90% and a benzaldehyde selectivity of 86.1%. These achievements were attained at 360 °C, atmospheric pressure, a hydrogen to methyl benzoate molar ratio of 40:1, and a Gas Hourly Space Velocity (GHSV) of 800 h−1. This research underscores the potential for optimizing catalysts to enhance the efficiency and sustainability of benzaldehyde synthesis. [ABSTRACT FROM AUTHOR]

Ethyl salicylate (EtSA) and ethyl benzoate (EtBZ) as alternative extraction solvents have been evaluated for vortex-assisted surfactant-enhanced emulsification microextraction (VASEME) of target fungicides (e.g. carbendazim, thiabendazole, and fuberidazole) before the high-performance liquid chromatographic analysis. Under optimum conditions, the preconcentration factors about 16–28 (18–33) and limits of detection in the range of 0.01–0.1 µg/L were achieved for both extraction solvents. Good recoveries in the range of 76.2–118.4% (85.7–114.6%) with the acceptable relative standard deviation lower than 10.4 were obtained at the concentration evaluation of 20 µg/L and 50 µg/L each fungicide in different water sample matrices. As a result, the proposed extraction solvents can be used as an alternative to other related solvents like methyl salicylate (MeSA) and methyl benzoate (MeBZ) for the preconcentration of target fungicides. [ABSTRACT FROM AUTHOR]

Lily is one of the most important cut flowers in the world, with a rich floral fragrance. To further explore the fragrance emission mechanisms of lily cultivars, headspace solid-phase microextraction–gas chromatography–mass spectrometry (HS-SPME-GC-MS) and organic solvent extraction–gas chromatography–mass spectrometry (OSE-GC-MS) were used to unveil the volatile organic compounds (VOCs) and endogenous extracts of seven lily cultivars. Furthermore, real-time quantitative PCR (qRT-PCR) was used to determine the expression levels of two key genes (TPS and BSMT) related to the biosynthesis of monoterpenoids and methyl benzoate. The results show that forty-five VOCs were detected in the petals of seven lily cultivars, and the main compounds were monoterpenoids and phenylpropanoids/benzenoids. Dichloromethane was the best solvent for extracting the endogenous extracts of Lilium 'Viviana' petals and eighteen endogenous extracts were detected using dichloromethane to extract the petals of seven lily cultivars. Each compound's emission ratio (natural logarithm of the ratio of VOC content to endogenous extract content) was calculated, and linear regression analyses between emission ratios and boiling points were conducted. Significant linear negative correlations existed between the emission ratios and boiling points of compounds, and the regression equations' coefficients of determination (R2) were all greater than 0.7. TPS was expressed highly in 'Viviana', 'Pink News', and 'Palazzo', and BSMT was expressed highly in 'Pink News' and 'Palazzo'. Correlation analyses between the gene expression levels and the monoterpenoids and methyl benzoate contents found that the TPS expression levels have strong positive correlations with monoterpenoids content, while no correlations were found between the expression levels of BSMT and the contents of methyl benzoate. This study lays the foundation for research on the release patterns of VOCs in the flowers of Lilium, and the breeding of lilies for their floral fragrance. [ABSTRACT FROM AUTHOR]

Lily is a popular flower worldwide due to its elegant appearance and pleasant fragrance. Floral volatiles of lily are predominated by monoterpenes and benzenoids. While a number of genes for monoterpene biosynthesis have been characterized, the molecular mechanism underlying floral benzenoid formation in lily remains unclear. Here, we report on the identification and characterization of a novel BAHD acyltransferase gene that contributes to the biosynthesis of two related floral scent benzoate esters, ethyl benzoate and methyl benzoate, in the scented Lilium oriental hybrid 'Siberia'. The emission of both methyl benzoate and ethyl benzoate in L. 'Siberia' was found to be tepal-specific, floral development-regulated and rhythmic. Through transcriptome profiling and bioinformatic analysis, a BAHD acyltransferase gene designated LoAAT1 was identified as the top candidate gene for the production of ethyl benzoate. In vitro enzyme assays and substrate feeding assays provide substantial evidence that LoAAT1 is responsible for the biosynthesis of ethyl benzoate. It was interesting to note that in in vitro enzyme assay, LoAAT1 can also catalyze the formation of methyl benzoate, which is typically formed by the action of benzoic acid methyltransferase (BAMT). The lack of an expressed putative BAMT gene in the flower transcriptome of L. 'Siberia', together with biochemical and expression evidence, led us to conclude that LoAAT1 is also responsible for, or at least contributes to, the biosynthesis of the floral scent compound methyl benzoate. This is the first report that a member of the plant BAHD acyltransferase family contributes to the production of both ethyl benzoate and methyl benzoate, presenting a new mechanism for the biosynthesis of benzoate esters. [ABSTRACT FROM AUTHOR]

Methyl 2-(2-oxo-2H-chromen-4-ylamino)benzoate, C17H13NO4 (1), was prepared by condensation between 4-hydroxycoumarin and methyl 2-aminobenzoate. It crystallizes in the orthorhombic space group Pca21 at 300 K. The molecule of compound 1 consists of the 2H-chromen-2-one part connected by an amine moiety (-NH-) to the methyl benzoate ring. The supramolecular array is formed by hydrogen bonds between the aromatic ring and the O atoms of the lactone and ester portions. The structural details match the spectroscopic data acquired from NMR and IR spectroscopy. [ABSTRACT FROM AUTHOR]

In this paper the density functional theory (DFT) method was employed to investigate the cross‐coupling of methanol with benzyl alcohol to afford methyl benzoate, catalysed by Mn‐PNN pincer complex. The whole reaction process mainly includes three stages: the dehydrogenation of benzyl alcohol to benzaldehyde, the coupling of benzaldehyde with methanol to hemiacetal and the dehydrogenation of hemiacetal to methyl benzoate. The calculated results indicated that two dehydrogenation processes are influenced by two competitive mechanisms of inner and outer spheres. Dehydrogenation of benzyl alcohol to benzaldehyde is the rate‐determining step of the whole reaction, with the energy barrier of 22.1 kcal/mol. In addition, the regeneration of catalyst is also extremely important. Compared with direct dehydrogenation, the dehydrogenation mode assisted by formic acid is more advantageous. This work might provide theoretical insights and shed light on the design of cheap transition‐metal catalysts for the dehydrogenation reaction. [ABSTRACT FROM AUTHOR]

Cocoa pulp represents an interesting by-product of cocoa production, with an appealing flavor. We developed a non-alcoholic beverage via the submerged fermentation of 10% pasteurized cocoa pulp in water with Laetiporus persicinus for 48 h; the product was characterized by tropical fruity notes such as coconut, mango, passion fruit and peach. The overall acceptance of the beverage compared to the non-fermented medium, as rated by a panel, increased from 2.9 to 3.7 (out of 5.0 points) for odor and from 2.1 to 4.2 for taste. (R)-Linalool (flowery, fruity), methyl benzoate (green, sweet), 2-phenylethanol (rose, sweet), 5-butyl-2(5H)-furanone (coconut, peach) and (E)-nerolidol (flowery, woody) contributed to the overall aroma with odor activity values of >1. During aroma dilution analysis, further substances with coconut, passion fruit and peach-like notes were perceived and structurally assigned to the group of sesquiterpenoids. The fermentation generated a highly interesting beverage using only 10% of the valuable cocoa pulp. The aroma formation via the fungus L. persicinus on cocoa pulp is of great interest for further research as an example of the formation of substances not yet described in the literature. [ABSTRACT FROM AUTHOR]

The catalytic activity and cyclic catalysis of different methyl benzoates were studied by using a series of Lewis solid acid catalysts. The iron-supported zirconium/titanium solid acid catalysts were characterized using FTIR, SEM, XRD, and BET. The details of catalytic activity and cyclic catalysis verified that the catalyst catalyzed the reactions of 31 benzoic acids with different substituents and methanol. In addition, the mechanism was revealed according to the microstructure, acid strength, and specific surface area of the catalysts, and the yields of methyl benzoates by the GC-MS. Zr ions had significant effects on the catalytic activity of the catalyst. A certain proportion of Fe and Ti ions additionally enhanced the catalytic activity of the catalyst, with the catalyst-specific composition of Fe:Zr:Ti = 2:1:1 showing optimal catalytic activity. A variety of substituents in the benzene ring, such as the electron-withdrawing group, the electron-donating group, large steric hindrance, and the position of the group on the benzene ring, had regular effects on the catalytic activity of the methyl benzoates. An increase in the catalyst activity occurred owing to the increases in the catalyst surface and the number of acid sites after the Fe ion was added. The catalytic activity remained unchanged after the facile recycling method was performed. [ABSTRACT FROM AUTHOR]

Methyl benzoate (MB) compounds are prepared by reacting various benzoic acids with methanol using an acidic catalyst. In this study, the solid acids of zirconium metal solids fixed with various substances were studied. We determined that zirconium metal catalysts with fixed Ti had the best activity. The catalytic synthesis of a series of MB compounds using titanium zirconium solid acids was studied. The direct condensation of benzoic acid and methanol using a metallic Lewis acid without other auxiliary Bronsted acids is reported for the first time. [ABSTRACT FROM AUTHOR]

Michelia crassipes is a great ornamental plant, the flowers of which have high economic value. In this study, we employed headspace solid-phase microextraction (HS–SPME) combined with gas chromatography high-resolution mass spectrometry (GC–HRMS) for the first time to identify the volatile compounds emitted from different organs of M. crassipes flowers at different flowering stages. M. crassipes flower odor comprises 69 volatile compounds that are dominated by terpenes constituting 84% of collected volatiles. It was found that α-guaiene, β-caryophyllene and germacrene B had the highest relative amounts, while ethyl 3-methyl valerate, methyl benzoate and β-damascone had the highest odor activity values (OAVs). This contributed to the complex fruity, woody and floral aromas of M. crassipes. Total odor emission increased along the flower blooming, which was most abundant in the pistil followed by tepals and stamens. Paraffin sections of M. crassipes flower organs showed the highest density of oil secretory cells in the pistil at the full flowering stage, which was positively correlated with total odor release. The scent of the pistil and tepals was characterized by terpenes, whereas stamens was characterized by benzenoids. We suggest that the benzenoids in stamens might contribute to pollinator attraction in M. crassipes. [ABSTRACT FROM AUTHOR]

A new series of 3-(5-aryl-1-phenyl-1H-pyrazol-3-yl)-5-aryl-1,2,4-oxadiazole (9a–x) have been synthesized by a reaction of 5-aryl-N′-hydroxy-1-phenyl-1H-pyrazole-3-carboximidamide (7a–d) with substituted methyl benzoate (8a–f). The newly synthesized 3-(5-aryl-1-phenyl-1H-pyrazol-3-yl)-5-aryl-1,2,4-oxadiazole (9a–x) derivatives were characterized by spectroscopic techniques and screened for in vitro antibacterial activity against Gram-positive bacterial strains Bacillus subtilis (NCIM 2063), Staphylococcus albus (NCIM 2178). Gram-negative bacterial strains Escherichia coli (NCIM 2574), it was noticed that compounds 9h, 9i, and 9j in which R = 4-Cl and R1 = 2-Cl/4-Cl or 4-CH3 showed good activity against B. subtilis with MIC 31.25 μg/mL against standard S. albus having MIC 7.81 μg/mL. Proteus mirabilis (NCIM 2388) and in vitro antifungal activity against Aspergillus niger (ATCC 504) Candida albicans (NCIM 3100). 3-(5-Aryl-1-phenyl-1H-pyrazol-3-yl)-5-aryl-1,2,4-oxadiazole derivatives like compound 9a (R = H, R1 = 2-Cl), 9b (R = H, R1 = 2-Cl), 9d (R = H, R1 = 4-Cl), and 9k (R = 4-Cl, R1 = 4-OCH3) showed good activity against A. niger with MIC 31.25 µg/mL, which are comparable to standard drug ravuconazole having MIC 31.5 µg/mL. Compounds 9h (R = 4-Cl, R1 = 2-Cl) and 9j (R = 4-Cl, R1 = 4-CH3) showed activity against A. niger with MIC 7.81 µg/mL which is comparable to standard drug Fluconazole having MIC 7.81 µg/mL and fourfold more activity with respect to drug Ravuconazole. The antibacterial activity of 3-(5-aryl-1-phenyl-1H-pyrazol-3-yl)-5-aryl-1,2,4-oxadiazole (9a–x) derivatives led to the conclusion that these scaffolds could aid in the creation of lead drugs to treat microbial infection. [ABSTRACT FROM AUTHOR]

The herb of Trigonella caerulea (Fabaceae), commonly known as blue fenugreek, is used for the production of traditional cheese and bread varieties in the Alpine region. Despite its frequent consumption, only one study so far has focused on the constituent pattern of blue fenugreek, revealing qualitative information on some flavor-determining constituents. However, with regard to the volatile constituents present in the herb, the applied methods were insufficient and did not take relevant terpenoids into account. In the present study, we analyzed the phytochemical composition of T. caerulea herb applying a set of analytical methods, such as headspace-GC, GC-MS, LC-MS, and NMR spectroscopy. We thus determined the most dominant primary and specialized metabolites and assessed the fatty acid profile as well as the amounts of taste-relevant α-keto acids. In addition, eleven volatiles were quantified, of which tiglic aldehyde, phenylacetaldehyde, methyl benzoate, n-hexanal, and trans-menthone were identified as most significantly contributing to the aroma of blue fenugreek. Moreover, pinitol was found accumulated in the herb, whereas preparative works led to the isolation of six flavonol glycosides. Hence, our study shows a detailed analysis of the phytochemical profile of blue fenugreek and provides an explanation for its characteristic aroma and its health-beneficial effects. [ABSTRACT FROM AUTHOR]

It is hypothesized that in heterostylous plant species, standardization of signals of floral attraction between different morphs is advantageous, encouraging flower visitors to switch between morphs. It remains unclear whether signals of floral attraction (floral odor and properties of nectar) are similar between morphs in distylous species pollinated by hawkmoths, and how these relate to hawkmoth behavior. We observed the behavior of visitors to distylous Luculia pinceana (Rubiaceae), collected and analyzed floral odor, and examined properties of nectar (volume, sugar concentration, and composition) of long‐styled and short‐styled morphs during the day and night. Pollinator responses to the floral scent were tested with a Y‐tube olfactometer. We conducted diurnal and nocturnal pollination treatments and six other pollination treatments to test the importance of nocturnal pollinators and to examine the self‐incompatibility system. A species of hawkmoth, Cechenena lineosa, was the effective pollinator. The floral odor was rich in methyl benzoate, and sucrose was dominant in the nectar. There were no significant differences between the two morphs in the methyl benzoate content or the properties of nectar. Flowers released more methyl benzoate and secreted larger volumes of nectar with lower sugar concentration at night than during the day. The hawkmoth had a significant preference for methyl benzoate. Luculia pinceana was partially self‐incompatible and relied on nocturnal pollinators for reproductive success. This study verifies that floral attraction signals are consistent between different morphs in this distylous species, promoting compatible pollination, and the features and the diel pattern of these signals between day and night are adapted to hawkmoth behavior. [ABSTRACT FROM AUTHOR]

The main bottleneck in inkjet printing (IJP) is a stable and jettable ink formulation. This paper discusses the ink formulation for the small molecule phosphorescent dopant/host system. The study involves the estimation of Hansen solubility parameters (HSP) to formulate inkjet‐printed ink of an iridium complex‐based phosphorescent material, bis(4‐phenylthieno[3,2‐c]pyridinato‐N,C2') (acetylacetonate) iridium(III) (PO‐01) as dopant and 4, 40‐bis (carbazol‐9‐yl) biphenyl as the host of the emissive layer. Based on dopant and host HSP analyses, toluene and methyl benzoate are chosen as ink solvents. Our ink is stable for a month and can be replicated with great accuracy. The interaction of individual drops is examined in detail since resolution or film quality is highly influenced by the drop formation and spread on a substrate. Finally, an inkjet‐printed emissive layer is demonstrated on both glass and flexible substrates. The fabricated devices exhibit the maximum current efficiency and luminance of 6.4 cd A−1 and 5781 cd m−2. A technique is also shown to print large‐area organic light‐emitting diode (OLED) devices having different patterns without patterning or pixelization of the active area of the electrodes. Up to 80 × 80 mm2 large‐area OLED tiles are made using IJP of the emissive layer. [ABSTRACT FROM AUTHOR]

Quadruple-bond dimolybdenum complexes provide invaluable insight into the two-electron bond, with structural chemistry providing a foundation for examination of bond properties. The synthesis and solid-state structure of the quadruple-bonded dimolybdenum(II) complex tetra­kis­(μ-4-methyl­benzoato-κ²O:O′)bis[(tetra­hydro­furan-κO)molybdenum(II)] tetra­hydro­furan disolvate, [Mo2(C8H7O2)4(C4H8O)2]·2C4H8O, are presented. This complex crystallizes in a triclinic cell with low-symmetry space group P[\overline{1}]. The dimolybdenum paddlewheel structure comprises four methyl­benzoate ligands and two axial THF ligands. The dimolybdenum bond distance of 2.1012 (4) Å is exemplary of this class of compounds. [ABSTRACT FROM AUTHOR]

Floral fragrance is an important trait that contributes to the ornamental properties and pollination of crabapple. However, research on the physiological and molecular biology of the floral volatile compounds of crabapple is rarely reported. In this study, metabolomic and transcriptomic analyses of the floral volatile compounds of standard Malus robusta flowers (Mr), and progeny with strongly and weakly fragrant flowers (SF and WF, respectively), were conducted. Fifty-six floral volatile compounds were detected in the plant materials, mainly comprising phenylpropane/benzene ring-type compounds, fatty acid derivatives, and terpene compounds. The volatile contents were significantly increased before the early flowering stage (ES), and the contents of SF flowers were twice those of WF and Mr flowers. Odor activity values were determined for known fragrant volatiles and 10--11 key fragrant volatiles were identified at the ES. The predominant fragrant volatiles were methyl benzoate, linalool, leaf acetate, and methyl anthranilate. In the petals, stamens, pistil, and calyx of SF flowers, 26 volatiles were detected at the ES, among which phenylpropane/benzene ring-type compounds were the main components accounting for more than 75% of the total volatile content. Functional analysis of transcriptome data revealed that the phenylpropanoid biosynthesis pathway was significantly enriched in SF flowers. By conducting combined analyses between volatiles and differentially expressed genes, transcripts of six floral scent-related genes were identified and were associated with the contents of the key fragrant volatiles, and other 23 genes were potentially correlated with the key volatile compounds. The results reveal possible mechanisms for the emission of strong fragrance by SF flowers, and provide a foundation for improvement of the floral fragrance and development of new crabapple cultivars. [ABSTRACT FROM AUTHOR]

The compounds of the homologous series of n-alkyl benzoates (PhCOO-n-CnH2n+1) have a number of important applications. As for many low-volatile compounds, a few data on the vaporization thermodynamics of this class of compounds are available. Here we systemized and critically analyzed the available information on vapor pressures and vaporization enthalpies of short linear alkyl benzoates from methyl to pentyl and complemented these data by additional experimental investigation of long-chained compounds: the heat capacities and vapor pressures of pentadecyl, hexadecyl and heptadecyl benzoates were measured for the first time between 340 and 490 K using DSC and TG-FSC. Based on the experimental data and empirical approaches, we completely described the vaporization thermodynamics of a series of alkyl benzoates from methyl to eicosyl and established the correlation of some properties with the chain length. A way to predict the vaporization enthalpies and vapor pressures inside the homologous series in a wide temperature range was proposed and tested. [ABSTRACT FROM AUTHOR]

Soil microbes are an abundant source of enzymes with unique properties that may be useful for industrial applications. As most wild-type strains show low chlorogenic acid esterase expression and activity, and most microbes cannot be cultured in the laboratory, a metagenomic approach provides methods of identifying new enzymes. In this study, a gene encoding a chlorogenic acid esterase, named Tan410, was isolated from a soil metagenomic library and overexpressed in Escherichia coli BL21 (DE3). The recombinant enzyme, with a predicted molecular weight of 54.88 kDa, was purified to homogeneity. The Km and Vmax values for Tan410 were 1.26 mM and 0.33 mM min–1, respectively, with chlorogenic acid as the substrate. Its optimum temperature and pH for reaction were 30 °C and 7.5, respectively. The enzyme exhibited moderate thermostability and broad pH stability (3.0–10.0). Tan410 was also able to hydrolyse ethyl ferulate, methyl caffeate, propyl gallate, ethyl gallate, methyl vanillate, methyl benzoate, ethyl benzoate, methyl 2,5-dihydroxybenzoate, and methyl 3,5-dihydroxybenzoate, and it released caffeic and ferulic acids from agricultural byproducts (destarched wheat bran and coffee pulp). Tan140 has potential for industrial application in biomass valorization. [ABSTRACT FROM AUTHOR]

Methyl benzoate (MBe), a volatile organic molecule, has been shown to have insecticidal effects on a variety of agricultural, stored products, and urban arthropod pests in recent investigations. However, the toxicity of MBe against nontarget organisms has rarely been investigated. This study investigated the lethal and sublethal effects of MBe on the generalist predator Orius laevigatus (Fieber) (Hemiptera: Anthocoridae) via different exposure routes. This species is an important natural enemy of thrips, aphids, and mites in biological control programs globally. Acute toxicity bioassays conducted on O. laevigatus showed that the lethal median concentration (LC50) values of MBe for topical and residual toxicity were 0.73 and 0.94%, respectively, after 24 hr of exposure. Importantly, a sublethal concentration of MBe (LC30 = 0.51%) did not affect the survival and reproduction of O. laevigatus. In addition, prey consumption by O. laevigatus under different exposure conditions with varying densities of Aphis gossypii (Glover) (Hemiptera: Aphididae) adults demonstrated a good fit for a Type II functional response. The sublethal concentration of MBe did not affect the attack rate and handling time of O. laevigatus compared to untreated insects, nor did it affect the longevity and fecundity of O. laevigatus females. Thus, according to the International Organization for Biological Control, the sublethal MBe concentration for O. laevigatus is categorized as harmless and may be used in conjunction with this predator species for integrated control of many agricultural insect pests. Graphical Abstract [ABSTRACT FROM AUTHOR]

Two new biphenylpropanoids (1 and 2) were isolated from the rhizomes of Acorus tatarinowii Schott. The structures of compounds 1 and 2 were determined by means of extensive spectroscopic methods. Their structures were identified as (R)-3-[1-hydroxy-3-(3,4-dimethoxyphenyl)propan-2-yl]-4,5-dimethoxy methyl benzoate (1) and (R)-3-[1-hydroxy-3-(3,4-dimethoxyphenyl)propan-2-yl]-4,5-dimethoxy ethyl benzoate (2). In addition, the xanthine oxidase (XOD) inhibitory activity of the isolated compounds was reported. Compounds 1 and 2 exhibited weak XOD inhibitory activity in the test. [ABSTRACT FROM AUTHOR]

Paraoxonase 1 (PON1) can metabolize some compounds such as aromatic carboxylic acid and unsaturated aliphatic esters, arylesters, cyclic carbonate, plucuronide drugs, some carbamate insecticide classes, nerve gases, and lactone compounds. Methyl benzoate has recently been shown to display potent toxicity against several insect species. In the current study, we aimed to investigate the effect of the methyl benzoate compounds (1–17) on PON1 activity. Methyl benzoate compounds inhibited PON1 with KI values ranging from 25.10 ± 4.73 to 502.10 ± 64.72 μM. Compound 10 (methyl 4‐amino‐2‐bromo benzoate) showed the best inhibition (KI = 25.10 ± 4.73 μM). Furthermore, using the ADME‐Tox, Glide XP, and MM‐GBSA tools of the Schrödinger Suite 2021‐4, a complete ligand–receptor interaction prediction was performed to characterize the methyl benzoates (1–17), probable binding modalities versus the PON1. [ABSTRACT FROM AUTHOR]

Cholinesterase (ChE) inhibitors are an important group of drugs used in Alzheimer's, glaucoma, and myasthenia gravis. In recent years, cholinesterase inhibition potentials of compounds have been investigated in new drug discovery studies. In this study (5-formylfuran-2-yl) methyl 4-nitro benzoate (compound 1) and newly designed (5-formylfuran-2-yl) methyl 3,4-dimethoxybenzoate (compound 2) were synthesized. The chemical structures of the synthesized compounds were characterized by spectral data (HRMS, ¹H NMR, and 13C NMR). The ChE inhibitory activity of the compounds was evaluated using in vitro colorimetric Ellman method. Compound 1 and compound 2 exhibited inhibitory activity against AChE at IC50 values of 3.25 µM and 8.45 µM, respectively. Compound 1 and Compound 2 showed inhibitory activity against BuChE at IC50 values of 8.45 µM and 14.44 µM, respectively. In Docking simulations with 1EVE and 1P0I, the binding free energy scores of compound 1 were higher than the binding free energy scores of compound 2. In this respect, in silico molecular docking studies overlapped with in vitro enzyme inhibition studies. These derivatives can be used to develop new drugs such as cholinesterase inhibitors. [ABSTRACT FROM AUTHOR]

Phenolic acids represent a large collection of phytochemical molecules present in the plant kingdom; they have an important role as epigenetic regulators, particularly as inhibitors of DNA methylation. In the present study, 14 methyl benzoate and cinnamate analogs were synthesized (11–24). Their cytotoxic activity on hepatocellular carcinoma cells (Hep3B) and immortalized human hepatocyte cells was then evaluated. In addition, its effect on the inhibition of global DNA methylation in Hep3B was also determined. Our results showed that the cinnamic derivatives 11–14 and 20–22 were more potent than the free caffeic acid (IC50 109.7–364.2 µM), being methyl 3,4‐dihydroxycinammate (12) the most active with an IC50 = 109.7 ± 0.8 µM. Furthermore, 11–14, 20–23 compounds decreased overall DNA methylation levels by 63% to 97%. The analogs methyl 4‐hydroxycinnamate (11), methyl 3,4,5‐trimethoxycinnamate (14), methyl 4‐methoxycinnamate (21), and methyl 3,4‐dimethoxycinnamate (22) showed relevant activities of both cytotoxicity and global DNA methylation inhibition. The molecular docking of 21 and 14 suggested that they partly bind to the SAH‐binding pocket of DNA methyltransferase 1. These results emphasize the importance of natural products and their analogs as potential sources of DNA methylation modulating agents. [ABSTRACT FROM AUTHOR]

The aim of this study is to evaluate the phytochemical profile, oral acute toxicity, and the effect of ylang-ylang (Cananga odorata Hook. F. & Thomson) essential oil (YEO) on acute inflammation. YEO was analyzed by gas chromatography/mass spectrometry. For in vitro tests, YEO was assessed using cytotoxicity, neutrophil chemotaxis induced by N-formyl methionyl leucyl phenylalanine (fMLP), and phagocytic activity tests. YEO was orally administered in zymosan-induced peritonitis, carrageenan-induced leukocyte rolling, and adhesion events in the in situ microcirculation model and in carrageenan-induced paw edema models. YEO (2000 mg/kg) was also tested using an acute toxicity test in Swiss mice. YEO showed a predominance of benzyl acetate, linalool, benzyl benzoate, and methyl benzoate. YEO did not present in vitro cytotoxicity. YEO reduced the in vitro neutrophil chemotaxis induced by fMLP and reduced the phagocytic activity. The oral treatment with YEO reduced the leukocyte recruitment and nitric oxide production in the zymosan-induced peritonitis model, reduced rolling and adherent leukocyte number induced by carrageenan in the in situ microcirculation model, and reduced carrageenan-induced edema and mechanical hyperalgesia. YEO did not present signs of toxicity in the acute toxicity test. In conclusion, YEO affected the leukocyte activation, and presented antiedematogenic, anti-hyperalgesic, and anti-inflammatory properties. [ABSTRACT FROM AUTHOR]

Simple Summary: The stick tea thrip Dendrothrips minowai is a key pest in tea plantations in China. In recent years, plant-derived semiochemicals have attracted considerable attention as promising attractants for the management of thrips, due to their safety and low cost. In this study, compounds that have been reported to attract other thrips or emitted from tea plants were evaluated for their electroantennogram (EAG), behavioral tests and field trapping efficacy for D. minowai. The EAG relative response value of D. minowai evoked by p-anisaldehyde, 3-methyl butanal, (E)-β-ocimene, farnesene, nonanal, eugenol, (+)-α-pinene, limonene, (−)-α-pinene, and γ-terpinene was significantly higher than the other compounds. Meanwhile, p-anisaldehyde, eugenol, farnesene, methyl benzoate, 3-methyl butanal, (E)-β-ocimene, (−)-α-pinene, (+)-α-pinene, and γ-terpinene led to attraction or repellency responses of female D. minowai. In addition, trap capture numbers of female D. minowai on sticky traps baited with p-anisaldehyde, eugenol, farnesene, and 3-methyl butanal were significantly higher than the control in tea plantations. Overall, our results highlight the potential application of plant volatiles in the development of effective, eco-friendly lure formulations for use in the monitoring and management of thrips. The stick tea thrip (Dendrothrips minowai Priesner) is the main pest thrip in tea (Camellia sinensis) plantations in China, and seriously affects the quality and yield of tea. Plant-derived semiochemicals provide an alternative to pheromones as lures and these compounds possess powerful attractiveness. In this study, we selected 20 non-pheromone semiochemicals, including compounds that have been reported to attract other thrips and some volatiles emitted from tea plants as the potential attractant components for D. minowai. In electroantennogram (EAG) assays, 10 synthetic compounds (p-anisaldehyde, 3-methyl butanal, (E)-β-ocimene, farnesene, nonanal, eugenol, (+)-α-pinene, limonene, (−)-α-pinene, and γ-terpinene) elicited significant antennal responses in female D. minowai. In addition, a two-choice H-tube olfactometer bioassay showed that D. minowai displayed significant positive responses to eight compound dilutions (p-anisaldehyde, eugenol, farnesene, methyl benzoate, 3-methyl butanal, (E)-β-ocimene, (−)-α-pinene, and (+)-α-pinene) when compared with the solvent control at both 1 and 2 h. Moreover, γ-terpinene exhibited a significantly deterrent effect on D. minowai. Finally, trap catches of four compounds (p-anisaldehyde, eugenol, farnesene, and 3-methyl butanal, respectively) significantly increase in tea plantations. Among these, the maximum number of D. minowai collected by blue sticky traps baited with p-anisaldehyde was 7.7 times higher than the control. In conclusion, p-anisaldehyde, eugenol, farnesene, and 3-methyl butanal could significantly attract D. minowai in the laboratory and under field conditions, suggesting considerable potential as commercial attractants to control D. minowai populations. [ABSTRACT FROM AUTHOR]

The pentose phosphate pathway (PPP), whose products are vital in biosynthetic events, is targeted in the treatment of many diseases such as cancer and malaria. The objective of this study was to identify new PPP inhibitors. The inhibition effects of methyl 4‐amino benzoates on glucose 6‐phosphate dehydrogenase (G6PD) and 6‐phosphogluconate dehydrogenase (6PGD) were analyzed through in vitro experiments and molecular docking studies were used to estimate inhibition mechanisms. IC50 values of compounds were found between 100.8 and 430.8 μM for G6PD and 206 and 693.2 μM for 6PGD. Molecular docking analysis showed that compound 1 was found the most effective inhibitor against hG6PD and compound 4 had the highest inhibitory potency against h6PGD with the estimated binding energy of −6.71 and −7.61 kcal/mol, respectively. In conclusion, it was determined that in vitro and in silico outcomes of the study were highly correlated with each other. The structure of these benzoates may aid in the development of drugs that target the PPP. [ABSTRACT FROM AUTHOR]

Methyl 2-hydroxy-5-[(trimethylsilyl)ethynyl]benzoate and methyl 2-hydroxy-5-ethynylbenzoate have been synthesized, and the crystallographic data on these compounds are reported. Due to their planar molecular structures, both compounds are layered. At the same time, planar molecules do not form a stack packing. In methyl 2-hydroxy-5-ethynylbenzoate, molecules in a layer are bound by hydrogen bonds (including those involving the terminal proton of the ethynyl group). The IR spectra are reported, and the fundamental absorption bands are interpreted for both compounds. The photoluminescence spectrum of methyl 2-hydroxy-5-[(trimethylsilyl)ethynyl]benzoate is also recorded: the emission maxima in the solid state and in chloroform solution are located at ~566 and 500 nm, respectively. [ABSTRACT FROM AUTHOR]

Poly-L-lactic acid (PLLA) aerogel-based scaffolds were obtained from physical PLLA gels containing cyclopentanone (CPO) or methyl benzoate (BzOMe) molecules. An innovative single step method of solvent extraction, using supercritical CO2, was used to achieve cylindrical monolithic aerogels. The pore distribution and size, analyzed by SEM microscopy, were found to be related to the crystalline forms present in the physical nodes that hold the gels together, the stable α'-form and the metastable co-crystalline ε-form, detected in the PLLA/BzOMe and PLLA/CPO aerogels, respectively. A higher mechanical compressive strength was found for the PLLA/CPO aerogels, which exhibit a more homogenous porosity. In vitro biocompatibility tests also indicated that monolithic PLLA/CPO aerogels exhibited greater cell viability than PLLA/BzOMe aerogels. An improved biocompatibility of PLLA/CPO monolithic aerogels was finally observed by coating the surface of the aerogels with polydopamine (PDA) obtained by the in situ polymerization of dopamine (DA). The synergistic effect of biodegradable polyester (PLLA) and the biomimetic interface (PDA) makes this new 3D porous scaffold, with porosity and mechanical properties that are tunable based on the solvent used in the preparation process, attractive for tissue engineering applications. [ABSTRACT FROM AUTHOR]

In this note we report the synthesis of a doubly acylated cis-THF-diol product synthesised in three steps by the stereoselective RuO4-catalysed oxidative cyclisation of 1,5-hexadiene, followed by benzoylation and acetylation. This substance is one of the substrates chosen to probe a new developed oxidative procedure to transform bis-acylated THF-diols into bis-acylated 1,4-diketones. This new derivative was fully characterised by spectroscopic methods. [ABSTRACT FROM AUTHOR]

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The hydrogenation of esters catalyzed by a manganese complex of phosphine‐aminopyridine ligand was developed. Using this protocol, a variety of (hetero)aromatic and aliphatic carboxylates including biomass‐derived esters and lactones were hydrogenated to primary alcohols with 63–98% yields. The manganese catalyst was found to be active for the hydrogenation of methyl benzoate, providing benzyl alcohol with turnover numbers (TON) as high as 45,000. Investigation of catalyst intermediates indicated that the amido manganese complex was the active catalyst species for the reaction. [ABSTRACT FROM AUTHOR]

In this study, headspace solid‐phase microextraction coupled with gas chromatography‐mass spectrometry (HS‐SPME‐GC/MS) was used to identify individual volatile compounds in five jujube varieties, and E‐nose was used to identify their flavor. The results showed that a total of 45 volatile compounds were detected by GC‐MS in the five varieties, and the proportion of acids was the highest (38.29%–54.95%), followed by that of aldehydes (22.94%–47.93%) and esters (6.33%–26.61%). Moreover, different varieties had obviously different volatile components. E‐nose analysis showed that the R7 and R9 sensors were more sensitive to the aroma of jujube than other sensors. The strong response of R7 sensor was attributed to terpenes (or structurally similar substances) in jujube fruit, such as 1‐penten‐3‐one, 2‐octenal, (E)‐2‐heptanaldehyde, and (E)‐2‐hexenal and that of R9 sensor was attributed to the cyclic volatile components such as benzaldehyde, benzoic acid, and methyl benzoate. The multivariate data analysis (PCA, OPLS‐DA, and HCA) of the results of GC/MS and E‐nose showed that the five varieties could be divided into three groups: (1) Ziziphus jujuba Mill. cv. Huizao (HZ) and Z. jujuba cv. Junzao (JZ). Acids were the main volatile components for this group (accounting for 47.44% and 54.95%, respectively); (2) Z. jujuba cv. Hamidazao (HMDZ). This group had the most abundant volatile components (41), and the concentrations were also the highest (1285.43 µg/kg); (3) Winter jujube 1 (Z. jujuba cv. Dongzao, WJ1) and Winter jujube 2 (Z. jujuba cv. Dongzao, WJ2). The proportion of acids (38.38% and 38.29%) and aldehydes (40.35% and 38.19%) were similar in the two varieties. Therefore, the combination of headspace solid‐phase microextraction coupled with gas chromatography‐mass spectrometry and E‐nose could quickly and accurately identify the volatile components in jujube varieties from macro‐ and microperspectives. This study can provide guidance for the evaluation and distinguishing of jujube varieties and jujube cultivation and processing. [ABSTRACT FROM AUTHOR]