Mrinmoy Saha, Ph.D.
|2014||Department of Chemistry||Oregon State University, Corvallis, OR|
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|Nikolayevskiy H, Robello M, Scerba MT, et al. (2019) The structure-activity profile of mercaptobenzamides' anti-HIV activity suggests that thermodynamics of metabolism is more important than binding affinity to the target. European Journal of Medicinal Chemistry. 178: 818-837|
|Zheng H, Saha M, Appella DH. (2018) Synthesis of Fmoc-Protected ( S, S)- trans-Cyclopentane Diamine Monomers Enables the Preparation and Study of Conformationally Restricted Peptide Nucleic Acids. Organic Letters|
|Tagad HD, Debnath S, Clausse V, et al. (2018) Chemical features important for activity in a class of inhibitors targeting the Wip1 flap subdomain. Chemmedchem|
|Saha M, Scerba MT, Shank NI, et al. (2017) Probing Mercaptobenzamides as HIV Inactivators via Nucleocapsid Protein 7. Chemmedchem|
|Hartman TL, Yang L, Helfrick AN, et al. (2016) Preclinical evaluation of a mercaptobenzamide and its prodrug for NCp7-Targeted inhibition of human immunodeficiency virus. Antiviral Research|
|Saha M, Li X, Collett ND, et al. (2016) Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity. The Journal of Organic Chemistry|
|Veerasamy N, Carlson EC, Collett ND, et al. (2013) Enantioselective approach to quinolizidines: total synthesis of cermizine D and formal syntheses of senepodine G and cermizine C. The Journal of Organic Chemistry. 78: 4779-800|
|Saha M, Carter RG. (2013) Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine. Organic Letters. 15: 736-9|