Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Shaoman Zhou"'
Autor:
Longhu Zhou, Hongwang Zhang, Chengwei Li, Coralie De Schutter, Ozkan Sari, Seema Mengshetti, Shaoman Zhou, Mahesh Kasthuri, Steven J. Coats, Raymond F. Schinazi, Franck Amblard
Publikováno v:
ACS Omega, Vol 7, Iss 1, Pp 1452-1461 (2021)
Externí odkaz:
https://doaj.org/article/e014eeef2887439f89555878649fce6a
Autor:
Shaoman Zhou, Franck Amblard, Peng Liu, Zhe Yang, Iulia A. Kovari, Ladislau C. Kovari, Justin Hackett, Nicholas Spellmon, Raymond F. Schinazi, Benjamin D. Kuiper, Joseph S. Brunzelle, Kendall M. Muzzarelli
Publikováno v:
Biochemistry
Norovirus is the leading cause of acute gastroenteritis worldwide with a yearly reported 700 million cases driving a $60 billion global socioeconomic burden. With no United States Food and Drug Administration approved therapeutics and the chance for
Autor:
Sijia, Tao, Longhu, Zhou, Hongwang, Zhang, Shaoman, Zhou, Sheida, Amiralaei, Jadd, Shelton, Maryam, Ehteshami, Yong, Jiang, Franck, Amblard, Steven J, Coats, Raymond F, Schinazi
Publikováno v:
Nucleosides Nucleotides Nucleic Acids
β-D-2’-C-Methyl-2,6-diaminopurine ribonucleoside (2’-C-Me-DAPN) phosphoramidate prodrug (DAPN-PD) is a selective hepatitis C virus inhibitor that is metabolized intracellularly into two active metabolites: 2’-C-Methyl-DAPN triphosphate (2’-C
Autor:
Shaoman Zhou, Raymond F. Schinazi, Ahmed Khalil, Steven J. Coats, Reuben Ovadia, Leda Bassit, Seema Mengshetti, Franck Amblard, Hao Li, Coralie De Schutter
Publikováno v:
Bioorganicmedicinal chemistry. 27(4)
We report herein the synthesis and evaluation of a series of β-d-2'-deoxy-2'-α-chloro-2'-β-fluoro and β-d-2'-deoxy-2'-α-bromo-2'-β-fluoro nucleosides along with their corresponding phosphoramidate prodrugs. Key intermediates, lactols 11 and 12,
Autor:
Jack Yoon, Kendall M. Muzzarelli, Shaoman Zhou, Peng Liu, Benjamin D. Kuiper, Ladislau C. Kovari, Raymond F. Schinazi, Franck Amblard, Bryan Cox
A series of tripeptidyl transition state inhibitors with new P1 and warhead moieties were synthesized and evaluated in a GI-1 norovirus replicon system and against GII-4 and GI-1 norovirus proteases. Compound 19, containing a 6-membered ring at the P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21573d2e96ffb96a94814a3e21368387
https://europepmc.org/articles/PMC6425952/
https://europepmc.org/articles/PMC6425952/
Autor:
Peng Liu, Zhe Yang, Bradley J. Keusch, Ladislau C. Kovari, Shaoman Zhou, Benjamin D. Kuiper, Joshua Holcomb, Iulia A. Kovari, Franck Amblard, Raymond F. Schinazi, Kendall M. Muzzarelli
Publikováno v:
Infect Disord Drug Targets
BACKGROUND: Noroviruses are the leading cause of acute gastroenteritis worldwide. Norovirus proteases, which are responsible for cleavage of the viral polyprotein, have become an attractive drug target to treat norovirus infections. Genogroup II (GII
Autor:
Shaoman Zhou, Hongwang Zhang, Satish N. Chavre, Lavanya Bondada, Franck Amblard, Sheida Amiralaei, Peng Liu, Jong Hyun Cho, Hao Li, Chengwei Li, Maryam Ehteshami, Raymond F. Schinazi, Judy S. Mathew, Xiao Lu, Sebastien Boucle, Steven J. Coats, Ethel C. Garnier-Amblard, Jadd R. Shelton, Longhu Zhou
Publikováno v:
Antiviral Research. 102:119-147
Chutes and Ladders is an exciting up-and-down-again game in which players race to be the first to the top of the board. Along the way, they will find ladders to help them advance, and chutes that will cause them to move backwards. The development of
Publikováno v:
Journal of Medicinal Chemistry. 52:3397-3407
Chiral Z- and E-stereoisomers of (1,2-dihydroxyethyl)methylenecyclopropane analogues of 2'-deoxyadenosine and 2'-deoxyguanosine were synthesized, and their antiviral activity was investigated. (S)-Methylenecyclopropylcarbinol (16) was converted in se
Publikováno v:
Tetrahedron. 63:9406-9412
Synthesis of methylene-2-ethynylcyclopropane analogues of nucleosides 12a , 12b , 13a , and 13b is described. Ethyl methylenecyclopropane carboxylate 14 was hydroxymethylated to give alcohol 15 , which was reduced to diol 16 . Selective protection wi
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 26:231-243
Synthesis of fluorinated cyclopropavir analogues 13a, 13b, 14a, and 14b is described starting from alkene 15. Addition of carbene derived from dibromofluoromethane gave bromofluoro cyclopropane 16. Reduction (compound 17) followed by desilylation gav