30 results on '"Markwalder, Jay A."'
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2. Supplementary Table S3 from Identification of a nonkinase target mediating cytotoxicity of novel kinase inhibitors
3. Supplementary Methods from Identification of a nonkinase target mediating cytotoxicity of novel kinase inhibitors
4. Understanding and modulating cyclin-dependent kinase inhibitor specificity: molecular modeling and biochemical evaluation of pyrazolopyrimidinones as CDK2/cyclin A and CDK4/cyclin D1 inhibitors
5. A kinetic characterization of the glycosyltransferase activity of Escherichia coli PBP1b and development of a continuous fluorescence assay
6. Pyrazolo[3,4-d]pyrimidin-4-ones
7. Template-constrained cyclic peptides: design of high-affinity ligands for GPIIb/IIIa
8. Development of a series of novel o-phenylenediamine-based indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors
9. Identification and optimization of a novel series of indoleamine 2,3-dioxygenase inhibitors
10. The Species-Dependent Metabolism of Efavirenz Produces a Nephrotoxic Glutathione Conjugate in Rats
11. Synthesis and evaluation of analogs of Efavirenz (SUSTIVA TM) as HIV-1 reverse transcriptase inhibitors
12. Lipid II: Total synthesis of the bacterial cell wall precursor and utilization as a substrate for glycosyltransfer and transpeptidation by penicillin binding protein (PBP) 1b of Eschericia coli
13. ChemInform Abstract: Lipid II: Total Synthesis of the Bacterial Cell Wall Precursor and Utilization as a Substrate for Glycosyltransfer and Transpeptidation by Penicillin Binding Protein (PBP) 1b of Eschericia coli.
14. Synthesis and NMR conformational analysis of a β-turn mimic incorporated into gramicidin S
15. Identification of a nonkinase target mediating cytotoxicity of novel kinase inhibitors
16. Synthesis and Biological Evaluation of 1-Aryl-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-4-one Inhibitors of Cyclin-Dependent Kinases
17. Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3
18. Regulated Expression of the Escherichia coli lepB Gene as a Tool for Cellular Testing of Antimicrobial Compounds That Inhibit Signal Peptidase I In Vitro
19. Identification of selective inhibitors of cyclin dependent kinase 4
20. ChemInform Abstract: 3,3a-Diyhdropyrano[4,3,2-de]quinazolin-2(1H)-ones Are Potent Non-Nucleoside Reverse Transcriptase Inhibitors.
21. Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz
22. 3,3a-Dihydropyrano[4,3,2- de ]quinazolin-2(1 H )-ones are potent non-nucleoside reverse transcriptase inhibitors
23. Synthesis and evaluation of analogs of Efavirenz (SUSTIVATM) as HIV-1 reverse transcriptase inhibitors
24. One-Pot Conversion of α-Thioureido Esters to Imidazol-2-ones and Imidazole-2-thiones
25. Cyclic HIV Protease Inhibitors: Synthesis, Conformational Analysis, P2/P2‘ Structure−Activity Relationship, and Molecular Recognition of Cyclic Ureas
26. 3,3a-Dihydropyrano[4,3,2-de]quinazolin-2(1H)-ones are potent non-nucleoside reverse transcriptase inhibitors
27. Synthesis and NMR conformational analysis of a β-turn mimic incorporated into gramicidin S.
28. Regulated Expression of the Escherichia coli lepBGene as a Tool for Cellular Testing of Antimicrobial Compounds That Inhibit Signal Peptidase I In Vitro
29. Remote double stereodiffrentiation in macrocylizations of α-alkoxyallylstannanes
30. ChemInform Abstract: Lipid II: Total Synthesis of the Bacterial Cell Wall Precursor and Utilization as a Substrate for Glycosyltransfer and Transpeptidation by Penicillin Binding Protein (PBP) 1b of Eschericia coli.
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