Design and synthesis of novel depsipeptide inhibitors of human rhinovirus 3C protease.

被引：0

作者：

Marakovits, JT ^{[1
]}

Webber, SE ^{[1
]}

Dragovich, PS ^{[1
]}

Prins, TJ ^{[1
]}

Zhou, R ^{[1
]}

Fuhrman, SA ^{[1
]}

Patick, AK ^{[1
]}

Ford, CE ^{[1
]}

Brown, EL ^{[1
]}

Meador, JW ^{[1
]}

Worland, ST ^{[1
]}

Matthews, DA ^{[1
]}

Ferre, R ^{[1
]}

机构：

[1] Agouron Pharmaceut Inc, Med Chem, San Diego, CA 92121 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1999年 / 218卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

281-MEDI

引用

页码：U1011 / U1011

页数：1

共 50 条

[1] Homophthalimides are inhibitors of human rhinovirus 3C protease.
Jungheim, LN
Cohen, JD
Wang, QM
Johnson, RB
Villarreal, EC
Wakulchik, M
Loncharich, RJ
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 213 : 274 - MEDI
[2] Design and synthesis of irreversible depsipeptidyl human rhinovirus 3C protease inhibitors
Webber, SE
Marakovits, JT
Dragovich, PS
Prins, TJ
Zhou, R
Fuhrman, SA
Patick, AK
Matthews, DA
Lee, CA
Srinivasan, B
Moran, T
Ford, CE
Brothers, MA
Harr, JEV
Meador, JW
Ferre, RA
Worland, ST
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (20) : 2683 - 2686
[3] Design, synthesis, and evaluation of nonpeptidic inhibitors of human rhinovirus 3C protease
Webber, SE
Tikhe, J
Worland, ST
Fuhrman, SA
Hendrickson, TF
Matthews, DA
Love, RA
Patick, AK
Meador, JW
Ferre, RA
Brown, EL
DeLisle, DM
Ford, CE
Binford, SL
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (26) : 5072 - 5082
[4] Design, synthesis, and evaluation of azapeptides as substrates and inhibitors for human rhinovirus 3C protease
Venkatraman, S
Kong, JS
Nimkar, S
Wang, QM
Aubé, J
Hanzlik, RP
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1999, 9 (04) : 577 - 580
[5] Synthesis of glycopeptides potential inhibitors of human rhinovirus 3C Protease
Danalev, L.
Lubin-Germain, N.
Uziel, J.
Auge, J.
JOURNAL OF PEPTIDE SCIENCE, 2010, 16 : 56 - 56
[6] Design and structure-activity relationships of novel inhibitors of human rhinovirus 3C protease
Kawatkar, S. P.
Gagnon, M.
Hoesch, V.
Tiong-Yip, C.
Johnson, K.
Ek, M.
Nilsson, E.
Lister, T.
Olsson, L.
Patel, J.
Yu, Q.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (14) : 3248 - 3252
[7] Structure-based design and synthesis of macrocyclic human rhinovirus 3C protease inhibitors
Namoto, Kenji
Sirockin, Finton
Sellner, Holger
Wiesmann, Christian
Villard, Frederic
Moreau, Robert J.
Valeur, Eric
Paulding, Stephanie C.
Schleeger, Simone
Schipp, Kathrin
Loup, Joachim
Andrews, Lori
Swale, Ryann
Robinson, Michael
Farady, Christopher J.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2018, 28 (05) : 906 - 909
[8] Synthesis and evaluation of tripeptidyl α-ketoamides as human rhinovirus 3C protease inhibitors
Chen, SH
Lamar, J
Victor, F
Snyder, N
Johnson, R
Heinz, BA
Wakulchik, M
Wang, QM
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (20) : 3531 - 3536
[9] Human rhinovirus 3C protease inhibitors: recent developments
Wang, QM
EXPERT OPINION ON THERAPEUTIC PATENTS, 1998, 8 (09) : 1151 - 1156
[10] S-nitrosothiols as novel, reversible inhibitors of human rhinovirus 3C protease
Xian, M
Wang, QM
Chen, XC
Wang, K
Wang, PG
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (18) : 2097 - 2100

← 1 2 3 4 5 →