Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ngan B. Phung"'
Autor:
Zhiwei, Wen, Veronica, Salmaso, Young-Hwan, Jung, Ngan B, Phung, Varun, Gopinatth, Qasim, Shah, Alexandra T, Patterson, John C R, Randle, Zhoumou, Chen, Daniela, Salvemini, David I, Lieberman, Gregory S, Whitehead, Tadeusz P, Karcz, Donald N, Cook, Kenneth A, Jacobson
Publikováno v:
J Med Chem
High affinity phenyl-piperidine P2Y(14)R antagonist 1 (PPTN) was modified with piperidine bridging moieties to probe receptor affinity and hydrophobicity. Various 2-azanorbornane, nortropane, isonortropane, isoquinuclidine, and ring-opened cyclopenty
Autor:
Kenneth A. Jacobson, Donald N. Cook, Tadeusz P Karcz, John C R Randle, John M. Bennett, Varun Gopinatth, Zhiwei Wen, Ngan B. Phung, Daniela Salvemini, Young-Hwan Jung, David I. Lieberman, Veronica Salmaso, Zhoumou Chen
Publikováno v:
Journal of Medicinal Chemistry. 64:5099-5122
A known zwitterionic, heterocyclic P2Y14R antagonist 3a was substituted with diverse groups on the central phenyl and terminal piperidine moieties, following a computational selection process. The most potent analogues contained an uncharged piperidi
Autor:
Fatma Mufti, Young‐Hwan Jung, Luigino A. Giancotti, Jinha Yu, Zhoumou Chen, Ngan B. Phung, Kenneth A. Jacobson, Daniela Salvemini
Publikováno v:
The FASEB Journal. 36
Autor:
Kenneth A. Jacobson, Fatma Mufti, Ngan B. Phung, Luigino Antonio Giancotti, Daniela Salvemini, Young-Hwan Jung, Jinha Yu, Zhoumou Chen
Publikováno v:
ACS Medicinal Chemistry Letters. 11:1281-1286
Eight P2Y14R antagonists, including three newly synthesized analogues, containing a naphthalene or phenyl-triazolyl scaffold were compared in a mouse model of chronic neuropathic pain (sciatic constriction). P2Y14R antagonists rapidly (≤30 min) rev
Autor:
Zhiwei Wen, Veronica Salmaso, Young-Hwan Jung, Ngan B. Phung, Varun Gopinatth, Qasim Shah, Alexandra T. Patterson, John C. R. Randle, Zhoumou Chen, Daniela Salvemini, David I. Lieberman, Gregory S. Whitehead, Tadeusz P. Karcz, Donald N. Cook, Kenneth A. Jacobson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08a16138dcf66e0cf8b0d97c43fac4e0
http://hdl.handle.net/11577/3459804
http://hdl.handle.net/11577/3459804
Autor:
Young-Hwan, Jung, Veronica, Salmaso, Zhiwei, Wen, John M, Bennett, Ngan B, Phung, David I, Lieberman, Varun, Gopinatth, John C R, Randle, Zhoumou, Chen, Daniela, Salvemini, Tadeusz P, Karcz, Donald N, Cook, Kenneth A, Jacobson
Publikováno v:
J Med Chem
A known zwitterionic, heterocyclic P2Y(14)R antagonist 3a was substituted with diverse groups on the central phenyl and terminal piperidine moieties, following a computational selection process. The most potent analogues contained an uncharged piperi
Autor:
Young-Hwan, Jung, Shanu, Jain, Varun, Gopinatth, Ngan B, Phung, Zhan-Guo, Gao, Kenneth A, Jacobson
Publikováno v:
Bioorg Med Chem Lett
Various 6-alkynyl analogues of a known 3-nitro-2-(trifluoromethyl)-2H-chromene antagonist 3 of the G(q)-coupled P2Y(6) receptor (P2Y(6)R) were synthesized using a Sonogashira reaction to replace a 6-iodo group. The analogues were tested in a function
Autor:
Steven Dudas, Zhan-Guo Gao, Jinha Yu, Zhiwei Wen, Tadeusz P Karcz, John M. Bennett, Kenneth A. Jacobson, Sierra Duca, Ngan B. Phung, Daniela Salvemini, Young-Hwan Jung, Veronica Salmaso, Donald N. Cook, Zhoumou Chen
Publikováno v:
J Med Chem
Various heteroaryl and bicyclo-aliphatic analogues of zwitterionic biaryl P2Y(14) receptor (P2Y(14)R) antagonists were synthesized, and affinity was measured in P2Y(14)R-expressing Chinese hamster ovary cells by flow cytometry. Given this series’ l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07e1e7f295e8914ed6cd6052e64fe4cb
https://europepmc.org/articles/PMC8040948/
https://europepmc.org/articles/PMC8040948/
Autor:
Kiran S. Toti, Anna Junker, Ngan B. Phung, Shanu Jain, Paola Oliva, Varun Gopinatth, Kenneth A. Jacobson, Mirko Scortichini, Clemens Dobelmann
Publikováno v:
Bioorg Med Chem Lett
The G(q)-coupled P2Y(6) receptor (P2Y(6)R) is a component of the purinergic signaling system and functions in inflammatory, cardiovascular and metabolic processes. UDP, the native P2Y(6)R agonist and P2Y(14)R partial agonist, is subject to hydrolysis
Autor:
Zhan-Guo Gao, Ngan B. Phung, Shanu Jain, Varun Gopinatth, Kenneth A. Jacobson, Young-Hwan Jung
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 41:128008
Various 6-alkynyl analogues of a known 3-nitro-2-(trifluoromethyl)-2H-chromene antagonist 3 of the Gq-coupled P2Y6 receptor (P2Y6R) were synthesized using a Sonogashira reaction to replace a 6-iodo group. The analogues were tested in a functional ass