-
2
-
-
0020596551
-
Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS)
-
F Barre-Sinoussi JC Chermann F Rey MT Nugeyre S Chamaret J Gruest C Dauguet C Axler-Blin F Vezinet-Brun C Rouzioux W Rozenbaum L Montagnier 1983 Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS) Science 220 868 871
-
(1983)
Science
, vol.220
, pp. 868-871
-
-
Barre-Sinoussi, F.1
Chermann, J.C.2
Rey, F.3
Nugeyre, M.T.4
Chamaret, S.5
Gruest, J.6
Dauguet, C.7
Axler-Blin, C.8
Vezinet-Brun, F.9
Rouzioux, C.10
Rozenbaum, W.11
Montagnier, L.12
-
3
-
-
0028850110
-
Phenylethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs
-
FW Bell AS Cantrell M Hogberg SR Jaskunas NG Johansson CL Jordan MD Kinnic P Lind JM Morin R Noreen B Oberg JA Palkowitz CA Parrish P Pranc C Sahlberg RJ Ternansky RT Vasileff L Vrang SJ West H Zhang XX Zhou 1995 Phenylethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs J Med Chem 38 4929 4936
-
(1995)
J Med Chem
, vol.38
, pp. 4929-4936
-
-
Bell, F.W.1
Cantrell, A.S.2
Hogberg, M.3
Jaskunas, S.R.4
Johansson, N.G.5
Jordan, C.L.6
Kinnic, M.D.7
Lind, P.8
Morin, J.M.9
Noreen, R.10
Oberg, B.11
Palkowitz, J.A.12
Parrish, C.A.13
Pranc, P.14
Sahlberg, C.15
Ternansky, R.J.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
Zhou, X.X.21
more..
-
4
-
-
0037920567
-
Three-dimensional quantitative structure-activity relationship analyses using comparative molecular field analysis and comparative molecular similarity indices analysis to elucidate selectivity differences of inhibitors binding to trypsin, thrombin, and factor Xa
-
M Bohm J Sturzebecher G Klebe 1999 Three-dimensional quantitative structure-activity relationship analyses using comparative molecular field analysis and comparative molecular similarity indices analysis to elucidate selectivity differences of inhibitors binding to trypsin, thrombin, and factor Xa J Med Chem 42 458 477
-
(1999)
J Med Chem
, vol.42
, pp. 458-477
-
-
Bohm, M.1
Sturzebecher, J.2
Klebe, G.3
-
5
-
-
0037075132
-
CoMFA and CoMSIA 3D QSAR and docking studies on conformationally- restrained cinnamoyl HIV-1 integrase inhibitors: Exploration of a binding mode at the active site
-
JK Buolamwini H Assefa 2002 CoMFA and CoMSIA 3D QSAR and docking studies on conformationally-restrained cinnamoyl HIV-1 integrase inhibitors: Exploration of a binding mode at the active site J Med Chem 45 841 852
-
(2002)
J Med Chem
, vol.45
, pp. 841-852
-
-
Buolamwini, J.K.1
Assefa, H.2
-
6
-
-
10244222420
-
Phenylethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs
-
AS Cantrell P Engelhardt M Hogberg SR Jaskunas NG Johansson CL Jordan MD Kinnic P Lind JM Morin R Noreen B Oberg JA Palkowitz CA Parrish P Pranc C Sahlberg RJ Ternansky RT Vasileff L Vrang SJ West H Zhang 1996 Phenylethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs J Med Chem 39 4261 4274
-
(1996)
J Med Chem
, vol.39
, pp. 4261-4274
-
-
Cantrell, A.S.1
Engelhardt, P.2
Hogberg, M.3
Jaskunas, S.R.4
Johansson, N.G.5
Jordan, C.L.6
Kinnic, M.D.7
Lind, P.8
Morin, J.M.9
Noreen, R.10
Oberg, B.11
Palkowitz, J.A.12
Parrish, C.A.13
Pranc, P.14
Sahlberg, C.15
Ternansky, R.J.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
more..
-
9
-
-
84988115618
-
Validation of the general purpose tripos 5.2 force field
-
M Clark RD Cramer III: NV Opdenbosch 1989 Validation of the general purpose tripos 5.2 force field J Comput Chem 10 982 1012
-
(1989)
J Comput Chem
, vol.10
, pp. 982-1012
-
-
Clark, M.1
Cramer III, R.D.2
Opdenbosch, N.V.3
-
10
-
-
0029011730
-
Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
-
E De Clercq 1995 Toward improved anti-HIV chemotherapy: therapeutic strategies for intervention with HIV infections J Med Chem 38 2491 2517
-
(1995)
J Med Chem
, vol.38
, pp. 2491-2517
-
-
De Clercq, E.1
-
11
-
-
0032946731
-
Three-dimensional quantitative structure-activity relationship study on cyclic urea derivatives as HIV-1 protease inhibitors: Application of comparative molecular field analysis
-
AK Debnath 1999 Three-dimensional quantitative structure-activity relationship study on cyclic urea derivatives as HIV-1 protease inhibitors: Application of comparative molecular field analysis J Med Chem 42 249 259
-
(1999)
J Med Chem
, vol.42
, pp. 249-259
-
-
Debnath, A.K.1
-
12
-
-
0021261510
-
Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS
-
RC Gallo SZ Salahuddin M Popovic GM Shearer M Kaplan BF Haynes TJ Palker R Redfield J Oleske B Safai 1984 Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS Science 224 500 503
-
(1984)
Science
, vol.224
, pp. 500-503
-
-
Gallo, R.C.1
Salahuddin, S.Z.2
Popovic, M.3
Shearer, G.M.4
Kaplan, M.5
Haynes, B.F.6
Palker, T.J.7
Redfield, R.8
Oleske, J.9
Safai, B.10
-
13
-
-
0033006546
-
Comparison of azacyclic urea A-98881 as HIV-1 protease inhibitor with cage dimeric N-benzyl 4-(4-methozyphenyl)-1, 4-dihydropyridine as representative of a novel class of HIV-1 protease inhibitors: A molecular modeling study
-
A Hilgeroth R Fleischer M Wiese FW Heinemann 1999 Comparison of azacyclic urea A-98881 as HIV-1 protease inhibitor with cage dimeric N-benzyl 4-(4-methozyphenyl)-1, 4-dihydropyridine as representative of a novel class of HIV-1 protease inhibitors: a molecular modeling study J Comput-Aided Mol Des 13 233 242
-
(1999)
J Comput-Aided Mol des
, vol.13
, pp. 233-242
-
-
Hilgeroth, A.1
Fleischer, R.2
Wiese, M.3
Heinemann, F.W.4
-
14
-
-
33748311541
-
QSAR analysis of indomethacin derivatives as selective COX-2 inhibitors
-
HK Jain RK Agrawal 2006 QSAR analysis of indomethacin derivatives as selective COX-2 inhibitors Internet Electron J Mol Des 5 224 236
-
(2006)
Internet Electron J Mol des
, vol.5
, pp. 224-236
-
-
Jain, H.K.1
Agrawal, R.K.2
-
15
-
-
33748329448
-
Inhibitory mode of 2-acetoxyphenyl alkyl sulfides against COX-1 and COX-2: QSAR analyses
-
HK Jain RK Agrawal 2006 Inhibitory mode of 2-acetoxyphenyl alkyl sulfides against COX-1 and COX-2: QSAR analyses Bioorg Med Chem Lett 16 5280 5284
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 5280-5284
-
-
Jain, H.K.1
Agrawal, R.K.2
-
16
-
-
0034676326
-
Computational studies on HIV-1 protease inhibitors: Influence of calculated inhibitor-enzyme binding affinities on the statistical quality of 3D-QSAR CoMFA models
-
PRN Jayatilleke AC Nair R Zauhar WJ Welsh 2000 Computational studies on HIV-1 protease inhibitors: Influence of calculated inhibitor-enzyme binding affinities on the statistical quality of 3D-QSAR CoMFA models J Med Chem 43 4446 4451
-
(2000)
J Med Chem
, vol.43
, pp. 4446-4451
-
-
Jayatilleke, P.R.N.1
Nair, A.C.2
Zauhar, R.3
Welsh, W.J.4
-
17
-
-
0027944195
-
Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity
-
G Klebe U Abraham T Mietzner 1994 Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity J Med Chem 37 4130 4146
-
(1994)
J Med Chem
, vol.37
, pp. 4130-4146
-
-
Klebe, G.1
Abraham, U.2
Mietzner, T.3
-
18
-
-
30344477669
-
QSAR by LFER model of HIV protease inhibitor mannitol derivatives using FA-MLR, PCRA and PLS techniques
-
JT Leonard K Roy 2006 QSAR by LFER model of HIV protease inhibitor mannitol derivatives using FA-MLR, PCRA and PLS techniques Bioorg Med Chem 14 1039 1046
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 1039-1046
-
-
Leonard, J.T.1
Roy, K.2
-
19
-
-
33746233230
-
Comparative QSAR modeling of CCR5 receptor binding affinity of substituted 1-(3,3-diphenylpropyl)-piperidinyl amides and ureas
-
JT Leonard K Roy 2006 Comparative QSAR modeling of CCR5 receptor binding affinity of substituted 1-(3,3-diphenylpropyl)-piperidinyl amides and ureas Bioorg Med Chem Lett 16 4467 4474
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 4467-4474
-
-
Leonard, J.T.1
Roy, K.2
-
20
-
-
18744427428
-
Biaryl acids: Novel non-nucleoside inhibitors of HIV reverse transcriptase types 1 and 2
-
J Milton MJ Slater AJ Bird D Spinks G Scott CE Price S Downing DVS Green S Madar R Bethell DK Stammers 1998 Biaryl acids: Novel non-nucleoside inhibitors of HIV reverse transcriptase types 1 and 2 Bioorg Med Chem Lett 8 2623 2628
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 2623-2628
-
-
Milton, J.1
Slater, M.J.2
Bird, A.J.3
Spinks, D.4
Scott, G.5
Price, C.E.6
Downing, S.7
Green, D.V.S.8
Madar, S.9
Bethell, R.10
Stammers, D.K.11
-
21
-
-
0037075124
-
Computational studies on tetrahydropyrimidine-2-one HIV-1 protease inhibitors: Improving three-dimensional quantitative structure-activity relationship comparative molecular field analysis models by inclusion of calculated inhibitor-and receptor based properties
-
AC Nair P Jayatilleke X Wang S Miertus WJ Welsh 2002 Computational studies on tetrahydropyrimidine-2-one HIV-1 protease inhibitors: improving three-dimensional quantitative structure-activity relationship comparative molecular field analysis models by inclusion of calculated inhibitor-and receptor based properties J Med Chem 45 973 983
-
(2002)
J Med Chem
, vol.45
, pp. 973-983
-
-
Nair, A.C.1
Jayatilleke, P.2
Wang, X.3
Miertus, S.4
Welsh, W.J.5
-
22
-
-
0034463939
-
Three-dimensional quantitative structure-activity relationships study on HIV-1 reverse transcriptase inhibitors in the class of dipyridodiazepinone derivatives, using comparative molecular field analysis
-
P Pungpo S Hannongbua 2000 Three-dimensional quantitative structure-activity relationships study on HIV-1 reverse transcriptase inhibitors in the class of dipyridodiazepinone derivatives, using comparative molecular field analysis J Mol Graphics Model 18 581 590
-
(2000)
J Mol Graphics Model
, vol.18
, pp. 581-590
-
-
Pungpo, P.1
Hannongbua, S.2
-
24
-
-
34548456464
-
QSAR study of novel 1, 1, 3 - Trioxo [1, 2, 4] - Thiadiazine (TTDs) analogues as potent anti-HIV agents
-
V Ravichandran VK Mourya RK Agrawal 2007 QSAR study of novel 1, 1, 3 - trioxo [1, 2, 4] - thiadiazine (TTDs) analogues as potent anti-HIV agents Arkivoc XIV 204 212
-
(2007)
Arkivoc
, vol.14
, pp. 204-212
-
-
Ravichandran, V.1
Mourya, V.K.2
Agrawal, R.K.3
-
25
-
-
38149038721
-
QSAR prediction of HIV-1 reverse transcriptase inhibitory activity of benzoxazinone derivatives
-
V Ravichandran VK Mourya RK Agrawal 2007 QSAR prediction of HIV-1 reverse transcriptase inhibitory activity of benzoxazinone derivatives Internet Electron J Mol Des 6 363 374
-
(2007)
Internet Electron J Mol des
, vol.6
, pp. 363-374
-
-
Ravichandran, V.1
Mourya, V.K.2
Agrawal, R.K.3
-
27
-
-
34948822189
-
QSAR analysis of caffeoyl naphthalene sulphonamide derivatives as HIV-1 Integrase inhibitors
-
KK Sahu V Ravichandran VK Mourya RK Agrawal 2007 QSAR analysis of caffeoyl naphthalene sulphonamide derivatives as HIV-1 Integrase inhibitors Med Chem Res 15 418 430
-
(2007)
Med Chem Res
, vol.15
, pp. 418-430
-
-
Sahu, K.K.1
Ravichandran, V.2
Mourya, V.K.3
Agrawal, R.K.4
-
28
-
-
0028785708
-
L-743, 726 (DMP-266): A novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase
-
SD Young SF Britcher LO Tran LS Payne WC Lumma TA Lyle JR Huff PS Anderson DB Olsen SS Carroll 1995 L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase Antimicrob Agents Chemother 39 2602 2605
-
(1995)
Antimicrob Agents Chemother
, vol.39
, pp. 2602-2605
-
-
Young, S.D.1
Britcher, S.F.2
Tran, L.O.3
Payne, L.S.4
Lumma, W.C.5
Lyle, T.A.6
Huff, J.R.7
Anderson, P.S.8
Olsen, D.B.9
Carroll, S.S.10
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