D. Srinivasa Reddy

Affiliations: 
2003-2007 Dr. Reddy's Laboratories 
 2007-2010 Advinus Therapeutics Pvt. Ltd 
 2010- CSIR-National Chemical Laboratory, Pune, India 
Area:
Total synthesis of natural products, medicinal chemistry
Website:
http://academic.ncl.res.in/ds.reddy/profile
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"D. Srinivasa Reddy"
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Publications

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Reddy DS, Jachak G, Athawale P, et al. (2019) Access to Stereoisomer Library of Solomonamide Macrocycles. Chemistry, An Asian Journal
Kalmode HP, Handore KL, Rajput R, et al. (2018) Total Synthesis and Biological Evaluation of Cell Adhesion Inhibitors Peribysin A and B: Structural Revision of Peribysin B. Organic Letters
Verma AK, Waghmare TS, Jachak GR, et al. (2018) Nitrosporeusine analogue ameliorates Chandipura virus induced inflammatory response in CNS via NFκb inactivation in microglia. Plos Neglected Tropical Diseases. 12: e0006648
Das P, Babbar P, Malhotra N, et al. (2018) Specific Stereoisomeric Conformations Determine the Drug Potency of Cladosporin Scaffold against Malarial Parasite. Journal of Medicinal Chemistry
Ramesh R, Reddy DS. (2017) Quest for Novel Chemical Entities through Incorporation of Silicon in Drug Scaffolds. Journal of Medicinal Chemistry
Thakare R, Singh AK, Das S, et al. (2017) Repurposing ivacaftor for treatment of staphylococcus aureus infections. International Journal of Antimicrobial Agents
Kalmode HP, Handore KL, Reddy DS. (2017) An Access to Fused Tricyclic γ-Butyrolactones, A Natural Product-like Scaffold. The Journal of Organic Chemistry
Philkhana SC, Verma AK, Jachak GR, et al. (2017) Identification of new anti-inflammatory agents based on nitrosporeusine natural products of marine origin. European Journal of Medicinal Chemistry. 135: 89-109
Philkhana SC, Mehrotra S, Murray TF, et al. (2016) Synthesis and biological evaluation of palmyrolide A macrocycles as sodium channel blockers towards neuroprotection. Organic & Biomolecular Chemistry
Pal S, Ramu V, Taye N, et al. (2016) GSH Induced Controlled Release of Levofloxacin form a Pur-pose-built Prodrug: Luminescence Response for Probing the Drug Release in E-coli and Staphylococcus aureus. Bioconjugate Chemistry
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