NOVEL AZA-CYCLIC UREAS THAT ARE POTENT INHIBITORS OF HIV PROTEASE .2.

被引：0

作者：

STEWART, KD ^{[1
]}

PARK, CH ^{[1
]}

KONG, XP ^{[1
]}

SHAM, HL ^{[1
]}

ZHAO, C ^{[1
]}

HERRIN, T ^{[1
]}

BETEBENNER, DA ^{[1
]}

ROSENBROOK, W ^{[1
]}

MADIGAN, D ^{[1
]}

LIN, SQ ^{[1
]}

SALDIVAR, A ^{[1
]}

WIDEBURG, NE ^{[1
]}

KEMPF, DJ ^{[1
]}

NORBECK, DW ^{[1
]}

机构：

[1] ABBOTT LABS,DIV PHARMACEUT PROD,ABBOTT PK,IL

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1995年 / 210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：

引用

页码：8 / MEDI

共 50 条

[41] 4-hydroxy-5,6-dihydropyrones .2. Potent non-peptide inhibitors of HIV protease
Tait, BD
Hagen, S
Domagala, J
Ellsworth, EL
Gajda, C
Hamilton, HW
Prasad, JVNV
Ferguson, D
Graham, N
Hupe, D
Nouhan, C
Tummino, PJ
Humblet, C
Lunney, EA
Pavlovsky, A
Rubin, J
Gracheck, SJ
Baldwin, ET
Bhat, TN
Erickson, JW
Gulnik, SV
Liu, BS
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (23) : 3781 - 3792
[42] Molecules - Novel HIV protease inhibitors
Lloyd, AW
DRUG DISCOVERY TODAY, 2000, 5 (09) : 427 - 427
[43] Highly potent HIV protease inhibitors with substituted oxindoles in P2′
Gulnik, S. V.
Afonina, El
Yokoe, H.
Yu, B.
Guerassina, T.
Silva, A. M.
Erickson, J. W.
Eissenstat, M.
ANTIVIRAL THERAPY, 2008, 13 (04) : A35 - A35
[44] Current and Novel Inhibitors of HIV Protease
Pokorna, Jana
Machala, Ladislav
Rezacova, Pavlina
Konvalinka, Jan
VIRUSES-BASEL, 2009, 1 (03): : 1209 - 1239
[45] Novel syntheses of HIV protease inhibitors
Judge, TM
Gammill, RB
Zhang, Q
Romines, KR
Lovasz, KD
Morris, JK
Luke, G
Morris, J
Chrusciel, RA
Tustin, JM
Phillips, G
Dolak, LA
Seest, EP
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 212 : 110 - ORGN
[46] From nonpeptide toward noncarbon protease inhibitors:: Metallacarboranes as specific and potent inhibitors of HIV protease
Cígler, P
Kozísek, M
Rezácová, P
Brynda, J
Otwinowski, Z
Pokorná, J
Plesek, J
Grüner, B
Dolecková-Maresová, L
Mása, M
Sedlácek, J
Bodem, J
Kräusslich, HG
Král, V
Konvalinka, J
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (43) : 15394 - 15399
[47] Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors
Dai, YJ
Guo, Y
Frey, RR
Ji, ZQ
Curtin, ML
Ahmed, AA
Albert, DH
Arnold, L
Arries, SS
Barlozzari, T
Bauch, JL
Bouska, JJ
Bousquet, PF
Cunha, GA
Glaser, KB
Guo, J
Li, JL
Marcotte, PA
Marsh, KC
Moskey, MD
Pease, LJ
Stewart, KD
Stoll, VS
Tapang, P
Wishart, N
Davidsen, SK
Michaelides, MR
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (19) : 6066 - 6083
[48] Synthesis of unsymmetric cyclic urea diols, a novel class of HIV protease inhibitors.
Stone, BRP
Harris, GD
Cann, RO
Smyser, TE
Confalone, PN
TETRAHEDRON LETTERS, 1998, 39 (34) : 6127 - 6130
[49] Nonsymmetrically substituted cyclic urea HIV protease inhibitors
Wilkerson, WW
Dax, S
Cheatham, WW
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (25) : 4079 - 4088
[50] Six-membered cyclic ureas as HIV-1 protease inhibitors: A QSAR study based on CODESSA PRO approach
Katritzky, AR
Oliferenko, A
Lomaka, A
Karelson, M
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (23) : 3453 - 3457

← 1 2 3 4 5 →