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Bioorganic & Medicinal Chemistry Letters|October 23, 2012
Investigations into specificity of azepinomycin for inhibition of guanase: discrimination between the natural heterocyclic inhibitor and its synthetic nucleoside analoguesSaibal Chakraborty, Niti H Shah, James C Fishbein, et al.
Bioorganic & Medicinal Chemistry Letters|December 25, 2010
A novel transition state analog inhibitor of guanase based on azepinomycin ring structure: Synthesis and biochemical assessment of enzyme inhibitionSaibal Chakraborty, Niti H Shah, James C Fishbein, et al.
Plos One|April 16, 2026
The tip of the iceberg: Profiling cooling agents using computational approaches to inform tobacco regulatory scienceSaibal Chakraborty, P Dilip Venugopal, Maria Kaltcheva, et al.
ACS Chemical Biology|July 21, 2016
Structure-Based Screening of Uncharted Chemical Space for Atypical Adenosine Receptor AgonistsDavid Rodríguez, Saibal Chakraborty, Eugene Warnick, et al.
Purinergic Signalling|January 29, 2020
Prevention and rescue of cardiac dysfunction by methanocarba adenosine monophosphonate derivativesJian-Bing Shen, Kiran S Toti, Saibal Chakraborty, et al.
Medchemcomm|February 10, 2018
Pyrimidine Nucleotides Containing a (S)-Methanocarba Ring as P2Y6 Receptor AgonistsKiran S Toti, Shanu Jain, Antonella Ciancetta, et al.
Computational and Structural Biotechnology Journal|May 15, 2015
John Daly Lecture: Structure-guided Drug Design for Adenosine and P2Y ReceptorsKenneth A Jacobson, Zhan-Guo Gao, Silvia Paoletta, et al.
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