Search Results - "Kummetha, Indrasena Reddy"
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Genome-Wide CRISPR Screen for Essential Cell Growth Mediators in Mutant KRAS Colorectal Cancers
Published in Cancer research (Chicago, Ill.) (15-11-2017)“…Targeting mutant KRAS signaling pathways continues to attract attention as a therapeutic strategy for KRAS-driven tumors. In this study, we exploited the power…”
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An efficient synthesis and biological screening of benzofuran and benzo[d]isothiazole derivatives for Mycobacterium tuberculosis DNA GyrB inhibition
Published in Bioorganic & medicinal chemistry (01-12-2014)“…[Display omitted] A series of twenty eight molecules of ethyl 5-(piperazin-1-yl)benzofuran-2-carboxylate and 3-(piperazin-1-yl)benzo[d]isothiazole were…”
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HIV-1 Escape from Small-Molecule Antagonism of Vif
Published in mBio (26-02-2019)“…The HIV-1 accessory protein Vif, which counteracts the antiviral action of the DNA-editing cytidine deaminase APOBEC3G (A3G), is an attractive and yet…”
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Discovery and Mechanism of SARS-CoV‑2 Main Protease Inhibitors
Published in Journal of medicinal chemistry (24-02-2022)“…The emergence of a new coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), presents an urgent public health crisis. Without available…”
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Rational Design and Optimization of m6A‑RNA Demethylase FTO Inhibitors as Anticancer Agents
Published in Journal of medicinal chemistry (25-08-2022)“…Aberrant regulation of N 6-methyladenosine (m6A) RNA modification has been implicated in the progression of multiple diseases, including cancer. Previously, we…”
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Rational Design and Optimization of m 6 A-RNA Demethylase FTO Inhibitors as Anticancer Agents
Published in Journal of medicinal chemistry (25-08-2022)Get full text
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1,2,3-Triazoles as Amide Bioisosteres: Discovery of a New Class of Potent HIV‑1 Vif Antagonists
Published in Journal of medicinal chemistry (25-08-2016)“…RN-18 based viral infectivity factor (Vif), Vif antagonists reduce viral infectivity by rescuing APOBEC3G (A3G) expression and enhancing A3G-dependent Vif…”
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Design, synthesis, biological evaluation of substituted benzofurans as DNA gyraseB inhibitors of Mycobacterium tuberculosis
Published in Bioorganic & medicinal chemistry (01-09-2014)“…DNA gyrase of Mycobacterium tuberculosis (MTB) is a type II topoisomerase and is a well-established and validated target for the development of novel…”
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Small-molecule PTPN2 Inhibitors Sensitize Resistant Melanoma to Anti-PD-1 Immunotherapy
Published in Cancer research communications (01-01-2023)“…Although immune checkpoint inhibitors targeting T-cell immunoregulatory proteins have revolutionized cancer treatment, they are effective only in a limited…”
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