23 results on '"Raghavan, Subharekha"'
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2. Identification of the Molecular Basis of Anti-fibrotic Effects of Soluble Guanylate Cyclase Activator Using the Human Lung Fibroblast Phosphoproteome
3. A highly stereoselective total synthesis of hispidospermidin: derivation of a pharmacophore model
4. Scavenging byproducts in the sulfoxide glycosylation reaction: application to the synthesis of ciclamycin O
5. Staurospine and ent-staurospine: the first total syntheses, prospects for a regioselective approach, and activity profiles
6. Selective Formation of Functionalized α-Quaternary Malononitriles toward 5,5-Disubstituted Pyrrolopyrimidinones
7. The discovery of high affinity agonists of GPR109a with reduced serum shift and improved ADME properties
8. GPR109a agonists. Part 2: Pyrazole-acids as agonists of the human orphan G-protein coupled receptor GPR109a
9. Anthranilic acid replacements in a niacin receptor agonist
10. Pyrazole acids as niacin receptor agonists for the treatment of dyslipidemia
11. GPR109a agonists. Part 1: 5-Alkyl and 5-aryl-pyrazole–tetrazoles as agonists of the human orphan G-protein coupled receptor GPR109a
12. Stereocontrolled total synthesis of hispidospermidin
13. First total synthesis of staurosporine and ent-staurosporine
14. Targeting native and apo-sGC
15. The synthesis and conformational analysis of amino acid–tetrahydroanthranilic acid hybrids
16. Tetrahydro anthranilic acid as a surrogate for anthranilic acid: Application to the discovery of potent niacin receptor agonists
17. A one-step synthesis of the ciclamycin trissacharide
18. Discovery of a Biaryl Cyclohexene Carboxylic Acid (MK-6892): A Potent and Selective High Affinity Niacin Receptor Full Agonist with Reduced Flushing Profiles in Animals as a Preclinical Candidate
19. Synthesis of novel HIV protease inhibitors (PI) with activity against PI-resistant virus
20. Design and synthesis of highly potent HIV protease inhibitors with activity against resistant virus
21. Combinatorial library of indinavir analogues: replacement for the aminoindanol at P2′
22. Scavenging Byproducts in the Sulfoxide Glycosylation Reaction: Application to the Synthesis of Ciclamycin 0
23. Combinatorial library of indinavir analogues: replacement for the aminoindanol at P2′
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