35 results on '"Zhong, Boyu"'
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2. Abstract 4027: TSN084, a multi-kinase inhibitor, overcomes acquired drug-resistant mutations of cMet, Trks, and Flt3, and displays broad activities against kinase oncotargets Axl, DDRs, and CDK8/19
3. Creep deformation and rupture behavior of CLAM steel at 823 K and 873 K
4. LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R, and other oncoproteins, and displays anti-tumor activities in mouse xenograft models
5. Meeting the potential emergency global drug supply challenge of hydroxychloroquine for COVID-19
6. Europium-labeled melanin-concentrating hormone analogues: ligands for measuring binding to melanin-concentrating hormone receptors 1 and 2
7. Design and synthesis of novel 3-sulfonylpyrazol-4-amino pyrimidines as potent anaplastic lymphoma kinase (ALK) inhibitors
8. Discovery of 2-arylamino-4-(1-methyl-3-isopropylsulfonyl-4-pyrazol-amino)pyrimidines as potent anaplastic lymphoma kinase (ALK) inhibitors
9. Abstract 2096: Bozitinib, a highly selective inhibitor of cMet, demonstrates robust activity in gastric, lung, hepatic and pancreatic in vivo models
10. Observations concerning the existence and reactivity of free alpha-amino aldehydes as chemical intermediates: evidence for epimerization-free adduct formation with various nucleophiles
11. Preparation of chiral, C-protected alpha-amino aldehydes of high optical purity and their use as condensation components in a linear synthesis strategy
12. Identification of the active site in bovine liver monoamine oxidase
13. Improved procedure for the synthesis of substituted beta-hydroxynitriles
14. LY2801653 is an orally bioavailable multi-kinase inhibitor with potent activity against MET, MST1R, and other oncoproteins, and displays anti-tumor activities in mouse xenograft models
15. Novel Route to the Synthesis of 4-Quinolyl Isothiocyanates.
16. Structure-based design of a new class of highly selective aminoimidazo[1,2-a]pyridine-based inhibitors of cyclin dependent kinases
17. Poly(ethylene glycol)-Supported Enzyme Inactivators. Efficient Identification of the Site of Covalent Attachment to α-Chymotrypsin by PEG-TPCK
18. Novel route to the synthesis of 4-quinolyl isothiocyanates
19. Asymmetric synthesis of chiral organofluorine compounds: Use of nonracemic fluoriodacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors
20. ChemInform Abstract: Synthesis of C-Protected α-Amino Aldehydes of High Enantiomeric Excess from Highly Epimerizable N-Protected α-Amino Aldehydes.
21. Synthesis of C-Protected α-Amino Aldehydes of High Enantiomeric Excess from Highly Epimerizable N-Protected α-Amino Aldehydes
22. ChemInform Abstract: Synthesis of Highly Epimerizable N‐Protected α‐Amino Aldehydes of High Enantiomeric Excess.
23. Observations Concerning the Existence and Reactivity of Free α-Amino Aldehydes as Chemical Intermediates: Evidence for Epimerization-Free Adduct Formation with Various Nucleophiles
24. Synthesis of highly epimerizable N-protected α-amino aldehydes of high enantiomeric excess
25. ChemInform Abstract: Preparation of Chiral, C‐Protected α‐Amino Aldehydes of High Optical Purity and Their Use as Condensation Components in a Linear Synthesis Strategy.
26. Anomalous Schmidt reaction products of phenylacetic acid and derivatives
27. Preparation of Chiral,C-Protected α-Amino Aldehydes of High Optical Purity and Their Use as Condensation Components in a Linear Synthesis Strategy
28. Syntheses of amino nitrones. Potential intramolecular traps for radical intermediates in monoamine oxidase-catalyzed reactions
29. Negativeion, Chemical-Ionization Mass Spectrometry of Sulfonic Acid Esters of Carbohydrates
30. An Improved Procedure for the Synthesis of Substituted β-Hydroxynitriles
31. Additions and corrections
32. Identification of the Active Site Cysteine in Bovine Liver Monoamine Oxidase B
33. Direct Continuous Fluorometric Assay for Monoamine Oxidase B
34. Rearrangement of aromatic sulfonate anions in the gas phase
35. Poly(ethylene glycol)-supported enzyme inactivators. Efficient identification of the site of covalent attachment to alpha-chymotrypsin by PEG-TPCK.
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