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• High-speed (~5 mm·s−1) continuous solution-shearing method was introduced to fabricate the large grained (>100 μm) perovskite thin films and their photovoltaic devices. • Only 3.5 μL of perovskite precursor solution was consumed for 4.25 cm2 film so that this shearing deposition is more environmentally eco-friendly approach compared to the spin-coating. • The hydrophobic top plate enables to deposit more densely packed films with less void formation, consequently leading to the improved photovoltaic performance. High-speed continuous deposition of solution-processed perovskite thin films with controlled microstructural morphology has been intensively pursued toward practical commercialization of high-efficiency perovskite solar cells. In order to meet this urgent demand in a timely manner, we present a rapid (~5 mm·s−1) scalable meniscus-controlled coating method to deposit large-grained (>100 μm) perovskite thin films over large area. Shearing movement of the meniscus of perovskite solution, confined by the hydrophobic-treated top and temperature-controlled bottom plates enables a rapid crystallization of perovskite grains, also facilitating the continuous influx of solutes at the meniscus for continuous film growth with less consumption of perovskite solution. Optical and structural analyses revealed that the rapid-shear-deposited perovskite thin films possess a large-grained, densely-packed and highly-crystalline phase. Consequently, perovskite solar cell based this film exhibits the power conversion efficiency of 10.9% even without compositional engineering and additive controls. Therefore, it can be claimed that this rapid shearing deposition of perovskite solution paves a way to achieve a cost-competitive production of the high-efficiency solar cell. [ABSTRACT FROM AUTHOR]

Graphical abstract Abstract Discovery of mutant-selective kinase inhibitors is one of the challenges in medicinal chemistry and is a main issue for epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors. We tried to improve the selectivity of pan-HER inhibitors for mutant EGFRs. Utilizing click chemistry, triazole-tethered quinazoline derivatives were synthesized, based on a quinazoline scaffold showing pan-HER inhibition. The representative compound 5j exhibited 17- and 52-fold improved selectivity for EGFR L858R/T790M over wild-type EGFR and HER2, respectively, and demonstrated 6.7-fold more potent antiproliferative activity against PC9 cells harboring EGFR-activating mutation than gefitinib. Although the described quinazolines did not surpass pyrimidines as 3rd generation EGFR inhibitors in terms of selectivity for mutant EGFRs, our approach might provide information that would help in the identification of mutant-selective compounds among pan-HER inhibitors using the quinazoline scaffold. [ABSTRACT FROM AUTHOR]

Cells in tissues encounter a range of physical cues as they migrate. Probing single cell and collective migratory responses to physically defined three-dimensional (3D) microenvironments and the factors that modulate those responses are critical to understanding how tissue migration is regulated during development, regeneration, and cancer. One key physical factor that regulates cell migration is topography. Most studies on surface topography and cell mechanics have been carried out with single migratory cells, yet little is known about the spreading and motility response of 3D complex multi-cellular tissues to topographical cues. Here, we examine the response to complex topographical cues of microsurgically isolated tissue explants composed of epithelial and mesenchymal cell layers from naturally 3D organized embryos of the aquatic frog Xenopus laevis . We control topography using fabricated micropost arrays (MPAs) and investigate the collective 3D migration of these multi-cellular systems in these MPAs. We find that the topography regulates both collective and individual cell migration and that dense MPAs reduce but do not eliminate tissue spreading. By modulating cell size through the cell cycle inhibitor Mitomycin C or the spacing of the MPAs we uncover how 3D topographical cues disrupt collective cell migration. We find surface topography can direct both single cell motility and tissue spreading, altering tissue-scale processes that enable efficient conversion of single cell motility into collective movement. [ABSTRACT FROM AUTHOR]

Abstract: 5,6,7,8-Tetrahydro-4H-cyclohepta[d]isoxazole derivatives were synthesized and evaluated as a novel class of inhibitors for α-melanocyte-stimulating hormone (α-MSH) induced melanogenesis in a mouse melanoma B16F10 cell line. Compound 8e (IC50 =0.67μM), 8h (IC50 =1.01μM) and 9b (IC50 =0.99μM) exhibited a potent inhibitory activity approximately 85- to 126-fold greater than kojic acid, a well-known potent inhibitor. A biochemical study indicates that the activity of this series should be displayed via down-regulation of the expression of tyrosinase. [Copyright &y& Elsevier]

Abstract: Phagocytosis and subsequent degradation of pathogens by macrophages play a pivotal role in host innate immune response to microbial infections. To find small molecule regulators for the investigation of complicated phagocytic process, we screened our in-house chemical library and found chemicals which inhibit phagocytosis of zymosan by macrophages. A representative compound 5a reduced phagocytosis of zymosan in both peritoneal macrophages and RAW264.7 cells in a dose-dependent manner. Treatment of 5a led to downregulate the key regulators of phagocytosis, Rac1, Rac2 and Cdc42, and slightly reduced phosphorylation of Akt by zymosan. [Copyright &y& Elsevier]

Abstract: 1,3,4-Oxadiazole derivatives were found to enhance astrocyte differentiation in rat fetal neural stem cells (NSCs). Differentiation activity was assessed by immunocytochemistry and analysis of mRNA expression of astrocyte markers, GFAP and S100. Compounds 7 and 8 showed approximately a two-fold increase in astrocyte differentiation without engagement of neuronal differentiation and detectable cytotoxicity. [Copyright &y& Elsevier]

Abstract: As a model compound for the transcription factor hijacking mechanism of action of DNA damaging agent that simultaneously bind to the nuclear receptor, we designed and synthesized a chimeric molecule, RA-mustard, which can bind with both retinoic acid receptor α (RARα) and DNA. The interaction between RA-mustard with RARα was confirmed by binding assay using RARα-overexpressing cell extract. RA-mustard-modified DNA diminished the RARα-dependent luciferase expression in the RARα-abundant cells. [Copyright &y& Elsevier]