Gregory Douglas Cuny
Affiliations: | 1992 | Pharmacological and Pharmaceutical Sciences | University of Houston, Houston, TX, United States |
Area:
medicinal chemistryWebsite:
http://www.uh.edu/pharmacy/directory-home/pps-faculty/greg-cuny/Google:
"Gregory Douglas Cuny"Mean distance: 7.29 | S | N | B | C | P |
Parents
Sign in to add mentorStephen L. Buchwald | grad student | 1992 | MIT | |
(The utilisation of zirconium intermediates and the development of hydroformylatlon processes in organic synthesis) |
Children
Sign in to add traineeAngela F. Ku | grad student | 2011-2016 | University of Houston |
Chalada Suebsuwong | grad student | 2012-2017 | University of Houston |
Sameer Nikhar | grad student | 2013-2018 | University of Houston |
Zhuming Sun | post-doc | 2012-2014 | University of Houston |
Mohana Rao Vippila | post-doc | 2012-2016 | University of Houston |
Yong Wang | post-doc | 2015-2016 | University of Houston |
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Publications
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Chen H, Lye MF, Gorgulla C, et al. (2023) A small molecule exerts selective antiviral activity by targeting the human cytomegalovirus nuclear egress complex. Plos Pathogens. 19: e1011781 |
Modi G, Marqus GM, Vippila MR, et al. (2021) The Enzymatic Activity of Inosine 5'-Monophosphate Dehydrogenase May Not Be a Vulnerable Target for Infections. Acs Infectious Diseases |
Nikhar S, Siokas I, Schlicher L, et al. (2021) Design of pyrido[2,3-d]pyrimidin-7-one inhibitors of receptor interacting protein kinase-2 (RIPK2) and nucleotide-binding oligomerization domain (NOD) cell signaling. European Journal of Medicinal Chemistry. 215: 113252 |
Lee S, Ku A, Rao Vippila M, et al. (2020) Mycophenolic anilides as broad specificity inosine-5'-monophosphate dehydrogenase (IMPDH) inhibitors. Bioorganic & Medicinal Chemistry Letters. 127543 |
Cuny GD, Degterev A. (2020) RIPK protein kinase family: Atypical lives of typical kinases. Seminars in Cell & Developmental Biology |
Suebsuwong C, Dai B, Pinkas DM, et al. (2020) Receptor-interacting protein kinase 2 (RIPK2) and nucleotide-binding oligomerization domain (NOD) cell signaling inhibitors based on a 3,5-diphenyl-2-aminopyridine scaffold. European Journal of Medicinal Chemistry. 200: 112417 |
Pawlowic MC, Somepalli M, Sateriale A, et al. (2019) Genetic ablation of purine salvage in reveals nucleotide uptake from the host cell. Proceedings of the National Academy of Sciences of the United States of America |
Ali G, Cuny GD. (2019) An efficient synthesis of an 8-phenoxy aporphine derivative utilizing mono-ligated palladium ortho-phenol arylation Tetrahedron. 75: 4318-4324 |
Kearney SE, Zahoránszky-Kőhalmi G, Brimacombe KR, et al. (2018) Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space. Acs Central Science. 4: 1727-1741 |
Jiang JK, Huang X, Shamim K, et al. (2018) Discovery of 3-(4-sulfamoylnaphthyl)pyrazolo[1,5-a]pyrimidines as potent and selective ALK2 inhibitors. Bioorganic & Medicinal Chemistry Letters |