Search Results - "Palde, Prakash B"
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Molecular Basis for Redox Activation of Epidermal Growth Factor Receptor Kinase
Published in Cell chemical biology (21-07-2016)“…Epidermal growth factor receptor (EGFR) is a target of signal-derived H2O2, and oxidation of active-site cysteine 797 to sulfenic acid enhances kinase…”
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2
A universal entropy-driven mechanism for thioredoxin–target recognition
Published in Proceedings of the National Academy of Sciences - PNAS (30-06-2015)“…Cysteine residues in cytosolic proteins are maintained in their reduced state, but can undergo oxidation owing to posttranslational modification during redox…”
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3
Safe and Efficient Tetrazole Synthesis in a Continuous-Flow Microreactor
Published in Angewandte Chemie International Edition (04-04-2011)“…Safer flow: The synthesis of 5‐substituted tetrazoles in flow (see scheme) is safe, efficient, scalable, requires no metal promoter, and uses a near‐equimolar…”
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Dynamic Combinatorial Selection of Molecules Capable of Inhibiting the (CUG) Repeat RNA−MBNL1 Interaction In Vitro: Discovery of Lead Compounds Targeting Myotonic Dystrophy (DM1)
Published in Journal of the American Chemical Society (03-12-2008)“…Myotonic dystrophy type 1 (DM1), the most common form of muscular dystrophy in adults, is an RNA-mediated disease. Dramatically expanded (CUG) repeats…”
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Selective Recognition of Alkyl Pyranosides in Protic and Aprotic Solvents
Published in Journal of the American Chemical Society (23-07-2008)“…The design and synthesis of receptors capable of selective, noncovalent recognition of carbohydrates continues to be a signature challenge in bioorganic…”
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Dissecting the molecular determinants of clinical PARP1 inhibitor selectivity for tankyrase1
Published in The Journal of biological chemistry (01-01-2021)“…Poly-ADP-ribosyltransferases play a critical role in DNA repair and cell death, and poly(ADP-ribosyl) polymerase 1 (PARP1) is a particularly important…”
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Substituted 4-methylquinolines as a new class of anti-tuberculosis agents
Published in Bioorganic & medicinal chemistry letters (24-03-2003)“…We report synthesis and anti-tuberculosis activities of a series of novel ring-substituted quinolines. The most effective compound of the series 3d (MIC=6.25…”
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Functional Site Discovery in a Sulfur Metabolism Enzyme by Using Directed Evolution
Published in Chembiochem : a European journal of chemical biology (04-10-2016)“…In human pathogens, the sulfate assimilation pathway provides reduced sulfur for biosynthesis of essential metabolites, including cysteine and…”
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First-in-Class Inhibitors of Sulfur Metabolism with Bactericidal Activity against Non-Replicating M. tuberculosis
Published in ACS chemical biology (15-01-2016)“…Development of effective therapies to eradicate persistent, slowly replicating M. tuberculosis (Mtb) represents a significant challenge to controlling the…”
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Characterization of Specific N -α-Acetyltransferase 50 (Naa50) Inhibitors Identified Using a DNA Encoded Library
Published in ACS medicinal chemistry letters (11-06-2020)“…Two novel compounds were identified as Naa50 binders/inhibitors using DNA-encoded technology screening. Biophysical and biochemical data as well as cocrystal…”
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Strategies for Recognition of Stem−Loop RNA Structures by Synthetic Ligands: Application to the HIV-1 Frameshift Stimulatory Sequence
Published in Journal of medicinal chemistry (26-08-2010)“…Production of the Gag-Pol polyprotein in human immunodeficiency virus (HIV) requires a −1 ribosomal frameshift, which is directed by a highly conserved RNA…”
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Synthesis and antimycobacterial activities of ring-substituted quinolinecarboxylic acid/ester analogues. Part 1
Published in Bioorganic & medicinal chemistry (01-08-2004)“…The antimycobacterial activities of ring-substituted quinolinecarboxylic acids/esters (Series 1–4) against M. tuberculosis H37Rv strains are described. The…”
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Ring-substituted quinolines. Part 2: Synthesis and antimycobacterial activities of ring-substituted quinolinecarbohydrazide and ring-substituted quinolinecarboxamide analogues
Published in Bioorganic & medicinal chemistry (15-12-2004)“…The antimycobacterial activities of ring-substituted quinolinecarbohydrazide and ring-substituted quinolinecarboxamide analogues (series 1–5) against M…”
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14
Safe and Efficient Tetrazole Synthesis in a Continuous-Flow Microreactor
Published in Angewandte Chemie (04-04-2011)“…Die Durchfluss‐Synthese von 5‐substituierten Tetrazolen (siehe Schema) gelingt sicher und effizient, benötigt keinen Metallpromotor, kommt mit einer annähernd…”
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15
universal entropy-driven mechanism for thioredoxinâtarget recognition
Published in Proceedings of the National Academy of Sciences - PNAS (2015)“…Cysteine residues in cytosolic proteins are maintained in their reduced state, but can undergo oxidation owing to posttranslational modification during redox…”
Get full text
Journal Article -
16
Safe and Efficient Tetrazole Synthesis in a Continuous‐Flow Microreactor
Published in Angewandte Chemie (04-04-2011)Get full text
Journal Article -
17
Strategies for Recognition of Stem-loop RNA Structures by Synthetic Ligands: Application to the HIV-1 Frameshift Stimulatory Sequencei
Published in Journal of medicinal chemistry (26-08-2010)“…Production of the Gag-Pol polyprotein in human immunodeficiency virus (HIV) requires a -1 ribosomal frameshift, which is directed by a highly conserved RNA…”
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18
Conformational and Structural Analysis of a ter-Cyclopentane Scaffold for Molecular Recognition
Published in European Journal of Organic Chemistry (01-01-2007)“…Well‐defined oligomers of cycloalkanes comprise a relatively unstudied class of organic compounds, and may have general utility in the development of receptors…”
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Book Review Journal Article -
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Corrigendum to “Ring-substituted quinolines. Part 2: Synthesis and antimycobacterial activities of ring-substituted quinolinecarbohydrazide and ring-substituted quinolinecarboxamide analogues”: [Bioorg. Med. Chem. 12 (2004) 6465]
Published in Bioorganic & medicinal chemistry (01-03-2005)Get full text
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