Structure-based drug design and the evaluation of irreversible HCV-protease inhibitors

被引：0

作者：

Qiao, Lixin ^{[1
]}

Niu, Deqiang ^{[1
]}

Zhu, Zhendong ^{[1
]}

Labenski, Matt ^{[1
]}

Hagel, Margit ^{[1
]}

St Martin, Thia ^{[1
]}

Sheet, Michael ^{[1
]}

Bernard, Hugues ^{[1
]}

Nacht, Mariana ^{[1
]}

Westlin, Willian ^{[1
]}

Petter, Russell ^{[1
]}

Singh, Juswinder ^{[1
]}

机构：

[1] Avila Therapeut Inc, Waltham, MA 02453 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2011年 / 242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：

102-MEDI

引用

页数：1

共 50 条

[1] Structure-based drug design of HIV protease inhibitors.
Navia, MA
Tung, RD
Chaturvedi, PR
Rao, BG
Partaledis, JA
Kim, EE
[J]. FASEB JOURNAL, 1996, 10 (06): : 2436 - 2436
[2] Structure-based drug design of novel peptidomimetic cellulose derivatives as HCV-NS3 protease inhibitors
Saleh, Noha A.
Elshemey, Wael M.
[J]. LIFE SCIENCES, 2017, 187 : 58 - 63
[3] Structure-based design of parasitic protease inhibitors
Li, RS
Chen, XW
Gong, BQ
Selzer, PM
Li, Z
Davidson, E
Kurzban, G
Miller, RE
Nuzum, EO
McKerrow, JH
Fletterick, RJ
Gillmor, SA
Craik, CS
Kuntz, ID
Cohen, FE
Kenyon, GL
[J]. BIOORGANIC & MEDICINAL CHEMISTRY, 1996, 4 (09) : 1421 - 1427
[4] STRUCTURE-BASED DESIGN OF ASPARTYL PROTEASE INHIBITORS
THAISRIVONGS, S
[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 209 : 20 - CINF
[5] Structure-based design of irreversible, peptidomimetic human rhinovirus 3C protease inhibitors
Dragovich, PS
Webber, SE
Fuhrman, SA
Patick, AK
Matthews, DA
Prins, TJ
Zhou, R
Marakovits, JT
Ford, CE
Meador, JW
Ferre, RA
Worland, ST
[J]. MEDICINAL CHEMISTRY INTO THE MILLENNIUM, 2001, (264): : 223 - 232
[6] Structure-based design of irreversible human rhinovirus 3C protease inhibitors.
Dragovich, PS
Webber, SE
Babine, RE
Fuhrman, SA
Patick, AK
Matthews, DA
Reich, SH
Prins, TJ
Marakovits, JT
Littlefield, ES
Zhou, R
Tikhe, J
Ford, CE
Wallace, MB
Bleckman, TM
Meador, JW
Ferre, RA
Brown, EL
Binford, SL
DeLisle, DM
Worland, ST
[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 215 : U863 - U863
[7] ITERATIVE PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF HIV PROTEASE INHIBITORS
KALISH, V
KALDOR, S
SHETTY, B
TATLOCK, J
DAVIES, J
HAMMOND, M
DRESSMAN, B
FRITZ, J
APPELT, K
REICH, S
MUSICK, L
WU, BW
SU, K
[J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1995, 30 : S201 - S214
[8] PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF NONPEPTIDIC HIV PROTEASE INHIBITORS
TATLOCK, JH
KALISH, VJ
DAVIES, J
APPELT, K
REICH, S
MUSICK, L
WU, B
KALDOR, S
[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 209 : 120 - MEDI
[9] PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF NONPEPTIDIC HIV PROTEASE INHIBITORS
GAJDA, C
DOMAGALA, J
TAIT, B
HAGEN, S
TUMINO, P
FERGUSON, D
PAVLOVSKY, A
RUBIN, J
LUNNEY, E
[J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1995, 210 : 21 - MEDI
[10] Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors
Scheidt, KA
Roush, WR
McKerrow, JH
Selzer, PM
Hansell, E
Rosenthal, PJ
[J]. BIOORGANIC & MEDICINAL CHEMISTRY, 1998, 6 (12) : 2477 - 2494

← 1 2 3 4 5 →