Saibal Chakraborty, Ph.D.
Affiliations: | 2011 | Chemistry | University of Maryland, Baltimore County, Baltimore, MD, United States |
Area:
Biochemistry, Organic ChemistryGoogle:
"Saibal Chakraborty"Mean distance: (not calculated yet)
Parents
Sign in to add mentorJames C. Fishbein | grad student | 2011 | UMBC | |
(Total synthesis and guanase inhibition studies of azepinomycin and its analogs.) |
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Publications
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Shah NH, Noe MR, Agnew-Heard KA, et al. (2021) Non-Targeted Analysis Using Gas Chromatography-Mass Spectrometry for Evaluation of Chemical Composition of E-Vapor Products. Frontiers in Chemistry. 9: 742854 |
Junker A, Renn C, Dobelmann C, et al. (2019) Structure-Activity Relationship of Purine and Pyrimidine Nucleotides as Ecto-5'-Nucleotidase (CD73) Inhibitors. Journal of Medicinal Chemistry |
Toti KS, Jain S, Ciancetta A, et al. (2017) Pyrimidine Nucleotides Containing a (S)-Methanocarba Ring as P2Y6 Receptor Agonists. Medchemcomm. 8: 1897-1908 |
Rodriguez D, Chakraborty S, Warnick E, et al. (2016) Structure-based screening of unchartered chemical space for atypical adenosine receptor agonists. Acs Chemical Biology |
Tantravedi S, Chakraborty S, Shah NH, et al. (2013) Analogs of iso-azepinomycin as potential transition-state analog inhibitors of guanase: synthesis, biochemical screening, and structure-activity correlations of various selectively substituted imidazo[4,5-e][1,4]diazepines. Bioorganic & Medicinal Chemistry. 21: 4893-903 |
Chakraborty S, Shah NH, Fishbein JC, et al. (2012) Investigations into specificity of azepinomycin for inhibition of guanase: discrimination between the natural heterocyclic inhibitor and its synthetic nucleoside analogues. Bioorganic & Medicinal Chemistry Letters. 22: 7214-8 |
Chakraborty S, Shah NH, Fishbein JC, et al. (2011) A novel transition state analog inhibitor of guanase based on azepinomycin ring structure: Synthesis and biochemical assessment of enzyme inhibition. Bioorganic & Medicinal Chemistry Letters. 21: 756-9 |