Search Results - "Bhat, Shridhar"
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1
Inhibition of eukaryotic translation elongation by cycloheximide and lactimidomycin
Published in Nature chemical biology (01-03-2010)“…Cycloheximide is a natural product that cell biologists have used for decades as a tool to arrest protein synthesis in eukaryotes. Biochemical data now refine…”
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2
XPB, a subunit of TFIIH, is a target of the natural product triptolide
Published in Nature chemical biology (01-03-2011)“…Triptolide is a bioactive natural product isolated from plants used in traditional Chinese medicine. A target identification approach shows that triptolide…”
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3
Three‐Component Synthesis of 3‐(Arylsulfonyl)benzothiophenes Using Acetic Acid as a Quencher for Methyl Radical‐Mediated Side Reactions
Published in Advanced synthesis & catalysis (12-05-2023)“…A one‐pot, three‐component synthesis of 3‐(arylsulfonyl)benzothiophenes was developed. The reaction did not require any catalysts or additives. The desired…”
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4
Hydrazide Mimics for Protein Lysine Acylation To Assess Nucleosome Dynamics and Deubiquitinase Action
Published in Journal of the American Chemical Society (01-08-2018)“…A range of acyl-lysine (acyl-Lys) modifications on histones and other proteins have been mapped over the past decade but for most, their functional and…”
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5
Disulfiram Reactivates Latent HIV-1 in a Bcl-2-Transduced Primary CD4+ T Cell Model without Inducing Global T Cell Activation
Published in Journal of Virology (01-06-2011)“…Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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6
The HBV Drug Entecavir — Effects on HIV-1 Replication and Resistance
Published in The New England journal of medicine (21-06-2007)“…Entecavir is a new antiviral medication to treat hepatitis B virus (HBV) infection. Initial in vitro studies suggested it had no activity against human…”
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Inhibition of eukaryotic translation elongation by the antitumor natural product Mycalamide B
Published in RNA (Cambridge) (01-08-2011)“…Mycalamide B (MycB) is a marine sponge-derived natural product with potent antitumor activity. Although it has been shown to inhibit protein synthesis, the…”
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Comorbid conditions responsible for the higher complications and poorer outcome in cardiac and vascular surgery: Time to reconsider hyperhomocysteinemia and its repercussions
Published in Indian journal of vascular and endovascular surgery (2019)“…Background: Plasma homocysteine is a perceived risk factor for the cardiovascular diseases. Many studies confirmed its remarkably high level with severity of…”
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9
Synthesis of antiproliferative flavones from calycopterin, major flavonoid of Calycopteris floribunda Lamk
Published in Bioorganic & medicinal chemistry (01-01-2011)“…Eighteen new analogues of the potent natural cytotoxic and antimitotic flavone 1 were synthesized from calycopterin 4. One of them, the 3′-amino analogue 5…”
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10
Novel glycosaminoglycan precursors as anti-amyloid agents, part III
Published in Journal of molecular neuroscience (01-01-2003)“…In vivo amyloids consist of two classes of constituents. The first is the disease-defining protein, e.g., amyloid beta (Abeta) in Alzheimer's disease (AD). The…”
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Short-Chain Aliphatic Polysulfonates Inhibit the Entry of Plasmodium into Red Blood Cells
Published in Antimicrobial Agents and Chemotherapy (01-08-2002)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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12
Rapamycin-inspired macrocycles with new target specificity
Published in Nature chemistry (01-03-2019)“…Rapamycin and FK506 are macrocyclic natural products with an extraordinary mode of action, in which they form binary complexes with FK506-binding protein…”
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13
Macromolecular crowding induces compaction and DNA binding in the disordered N-terminal domain of hUNG2
Published in DNA repair (01-02-2020)“…[Display omitted] Many human DNA repair proteins have disordered domains at their N- or C-termini with poorly defined biological functions. We recently…”
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14
Guanine-containing ssDNA and RNA induce dimeric and tetrameric structural forms of SAMHD1
Published in Nucleic acids research (11-12-2023)“…Abstract The dNTPase activity of tetrameric SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1) plays a critical role in…”
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15
Deoxyguanosine-Linked Bifunctional Inhibitor of SAMHD1 dNTPase Activity and Nucleic Acid Binding
Published in ACS chemical biology (20-10-2023)“…Sterile alpha motif histidine-aspartate domain protein 1 (SAMHD1) is a deoxynucleotide triphosphohydrolase that exists in monomeric, dimeric, and tetrameric…”
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16
Substituted oxines inhibit endothelial cell proliferation and angiogenesis
Published in Organic & biomolecular chemistry (21-04-2012)“…Two substituted oxines, nitroxoline (5) and 5-chloroquinolin-8-yl phenylcarbamate (22), were identified as hits in a high-throughput screen aimed at finding…”
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Catalyst‐Free, One‐Pot, Three‐Component Synthesis of 3‐Arylsulfonylated Thioflavones
Published in Advanced synthesis & catalysis (06-09-2022)“…A one‐pot, three‐component synthesis of 3‐arylsulfonylated thioflavones has been developed. The reactions were carried out without using any catalysts or…”
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18
Direct C3 Carbamoylation of 2H‐Indazoles
Published in European journal of organic chemistry (21-06-2021)“…We developed a novel method for direct C3 carbamoylation of 2H‐indazoles using oxamic acids as carbamoyl radical sources. In the presence of ammonium…”
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Inhibition of Angiogenesis by the Antifungal Drug Itraconazole
Published in ACS chemical biology (01-04-2007)“…Angiogenesis, the formation of new blood vessels, is implicated in a number of important human diseases, including cancer, diabetic retinopathy, and rheumatoid…”
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20
Structure-activity relationship study of itraconazole, a broad-range inhibitor of picornavirus replication that targets oxysterol-binding protein (OSBP)
Published in Antiviral research (01-08-2018)“…Itraconazole (ITZ) is a well-known, FDA-approved antifungal drug that is also in clinical trials for its anticancer activity. ITZ exerts its anticancer…”
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