Search Results - "Tangirala, Raghuram"
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Design and synthesis of functionalized piperazin-1yl-(E)-stilbenes as inhibitors of 17α-hydroxylase-C17,20-lyase (Cyp17)
Published in Bioorganic & medicinal chemistry letters (15-07-2018)“…[Display omitted] •Cyp17 (17α-hydroxylase-17,20-lyase) is a validated prostate cancer target.•Novel stilbenes disclosed herein are potent, selective inhibitors…”
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Discovery of Tetralones as Potent and Selective Inhibitors of Acyl-CoA:Diacylglycerol Acyltransferase 1
Published in ACS medicinal chemistry letters (08-02-2018)“…Acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) plays an important role in triglyceride synthesis and is a target of interest for the treatment of metabolic…”
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3
Design, synthesis, and evaluation of (2S,4R)-Ketoconazole sulfonamide analogs as potential treatments for Metabolic Syndrome
Published in Bioorganic & medicinal chemistry letters (01-12-2016)“…[Display omitted] Metabolic Syndrome, also referred to as ‘Syndrome X’ or ‘Insulin Resistance Syndrome,’ remains a major, unmet medical need despite over…”
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1‑(2-Hydroxy-2-methyl-3-phenoxypropanoyl)indoline-4-carbonitrile Derivatives as Potent and Tissue Selective Androgen Receptor Modulators
Published in Journal of medicinal chemistry (27-03-2014)“…We present a novel series of selective androgen receptor modulators (SARMs) which shows excellent biological activity and physical properties…”
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5
Synthesis of Privileged Scaffolds by Using Diversity-Oriented Synthesis
Published in Chemistry, an Asian journal (01-06-2013)“…An elegant reagent‐controlled strategy has been developed for the generation of a diverse range of biologically active scaffolds from a chiral bicyclic lactam…”
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Corrigendum: Synthesis of Privileged Scaffolds by Using Diversity-Oriented Synthesis
Published in Chemistry, an Asian journal (01-07-2014)Get full text
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7
Azaindolines: derisking the indoline structural alert
Published in Tetrahedron letters (25-01-2012)“…4-Substitued azaindolines, which are isosteres of indolines, are useful synthetic building blocks that reduce the risk of bioactivation induced idiosyncratic…”
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601 Development of improved small molecule STING agonists suitable for systemic administration
Published in Journal for immunotherapy of cancer (01-11-2020)“…BackgroundStimulator of Interferon Genes (STING) is a major player in the activation of robust innate immune response leading to initiation and enhancement of…”
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9
Synthesis and biological assays of E-ring analogs of camptothecin and homocamptothecin
Published in Bioorganic & medicinal chemistry (15-09-2006)“…Analogs of the anti-tumor agent camptothecin with both closed E-rings (lactone and ether) and open E-rings (reduced acid, hydrazide, and protected Weinreb…”
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Asymmetric total synthesis of (20 R)-homocamptothecin, substituted homocamptothecins and homosilatecans
Published in Tetrahedron (05-08-2002)“…An efficient asymmetric synthesis of a key DE lactone pyridone intermediate in the synthesis of homocamptothecin is reported. The synthesis is scalable and…”
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11
Total and semisynthesis and in vitro studies of both enantiomers of 20-fluorocamptothecin
Published in Bioorganic & medicinal chemistry letters (01-11-2005)“…Both enantiomers of 20-fluorocamptothecin and the racemate have been prepared by total synthesis. The ( R)-enantiomer is essentially inactive in a…”
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Abstract 1280: New generation of STING agonists: Development and characterization of a novel series of systemic immunomodulators with improved potency
Published in Cancer research (Chicago, Ill.) (01-07-2021)“…Abstract Background. Stimulator of interferon genes, known as STING, is an intracellular sensor of nucleic acids and one of key regulators in activating the…”
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Cascade radical cyclization: Application to the development of novel camptothecin analogs and a short synthesis of luotonin A and its analogs
Published 01-01-2005“…Cascade radical cyclizations have been employed in the synthesis of several novel analogs of camptothecin and luotonin A. The mild conditions of the…”
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Dissertation