-
1
-
-
10244222420
-
Phenethylthiazolylthiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and further structure-activity relationship studies of PETT anlogs
-
Cantrell, A. S.; Engelhardt, P.; Hogberg, M.; Jaskunas, S. R.; Johansson, N. G.; Jordan, C. L.; Kangasmetsa, J.; Kinnick, M. D.; Lind, P.; Morin, J. M. Jr.; Muesing, M. A.; Noreen, R.; Oberg, B.; Pranc, P.; Sahlberg, C.; Ternansky, R. J.; Vasileff, R. T.; Vrang, L.; West, S. J.; Zhang, H. Phenethylthiazolylthiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and further structure-activity relationship studies of PETT anlogs. J. Med. Chem. 1996, 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
Kangasmetsa, J.7
Kinnick, M.D.8
Lind, P.9
Morin Jr., J.M.10
Muesing, M.A.11
Noreen, R.12
Oberg, B.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..
-
2
-
-
0028850110
-
Phenethylthiazolylthiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT anlogs
-
Bell, F. W.; Cantrell, A. S.; Hogberg, M.; Jaskunas, S. R.; Johansson, N. G.; Jordan, C. L.; Kinnick, M. D.; Lind, P.; Morin, J. M. Jr.; Noreen, R.; Oberg, B.; Palkowitz, J. A.; Parrish, C. A.; Pranc, P.; Sahlberg, C.; Ternansky, R. T.; Vasileff, R. T.; Vrang, L.; West, S. J.; Zhang, H.; Zhou, X. X. Phenethylthiazolylthiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT anlogs. J. Med. Chem. 1995, 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
Kinnick, M.D.7
Lind, P.8
Morin Jr., 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.T.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
Zhou, X.X.21
more..
-
3
-
-
0032544145
-
Structure-based design of N-[2-(1-piperidinyl ethyl)]-N′-[2-(5- bromopyridyl)]-thiourea and N-[2-1-piperazmylethy10]-N′-[2-(5- bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Mao, C.; Vig, R.; Venkatachalam, T. K.; Sudbeck, E. A.; Uckun, F. M. Structure-based design of N-[2-(1-piperidinyl ethyl)]-N′-[2-(5- bromopyridyl)]-thiourea and N-[2-(1-piperazmylethy10]-N′-[2-(5- bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett. 1998, 8, 2213-2218.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2213-2218
-
-
Mao, C.1
Vig, R.2
Venkatachalam, T.K.3
Sudbeck, E.A.4
Uckun, F.M.5
-
4
-
-
0033532653
-
Rational design of N-[2-(2,5-dimethoxy phenylethyl)]-N′-[2-(5- bromopyridyl)]-thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus
-
Mao, C.; Sudbeck, E. A.; Venkatachalam, T. K.; Uckun, F. M. Rational design of N-[2-(2,5-dimethoxy phenylethyl)]-N′-[2-(5-bromopyridyl)]- thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus. Bioorg. Med. Chem. Lett. 1999, 9, 1593-1598.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 1593-1598
-
-
Mao, C.1
Sudbeck, E.A.2
Venkatachalam, T.K.3
Uckun, F.M.4
-
5
-
-
0034333415
-
Structure-based drug design of non-nucleoside inhibitors for wild-type and drug-resistant HIV reverse transcriptase
-
Mao, C.; Sudbeck, E. A.; Venkatachalam, T. K.; Uckun, F. M. Structure-based drug design of non-nucleoside inhibitors for wild-type and drug-resistant HIV reverse transcriptase. Biochem. Pharmacol. 2000, 60, 1251-1265.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 1251-1265
-
-
Mao, C.1
Sudbeck, E.A.2
Venkatachalam, T.K.3
Uckun, F.M.4
-
6
-
-
0033588963
-
N-[2-(1-cyclohexenyl)ethyl]-N′-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-cyclohexenyl)ethyl]-N′-[2-(5-chloropyridyl)]-thiourea as potent inhibitors of multi-drug resistant human immunodeficiency virus-1
-
Uckun, F. M.; Mao, C.; Pendergrass, S.; Maher, D.; Zhu, D.; Tuel-Ahlgren, L.; Venkatachalam, T. K. N-[2-(1-cyclohexenyl)ethyl]-N′-[2-(5- bromopyridyl)]-thiourea and N-[2-(1-cyclohexenyl)ethyl]-N′-[2-(5- chloropyridyl)]-thiourea as potent inhibitors of multi-drug resistant human immunodeficiency virus-1. Bioorg. Med. Chem. Lett. 1999, 9, 2721-2726.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2721-2726
-
-
Uckun, F.M.1
Mao, C.2
Pendergrass, S.3
Maher, D.4
Zhu, D.5
Tuel-Ahlgren, L.6
Venkatachalam, T.K.7
-
7
-
-
0034012087
-
N-[2-(4-methylphenyl)ethyl]-N′-[2-(5-bromopyridyl)]-thiourea as a potent inhibitor of NNRTI resistant and multi-drug resistant human immunodeficiency virus
-
Uckun, F. M.; Mao, C.; Pendergrass, S.; Maher, D.; Zhu, D.; Tuel-Ahlgren, L.; Venkatachalam, T. K. N-[2-(4-methylphenyl)ethyl]-N′-[2-(5- bromopyridyl)]-thiourea as a potent inhibitor of NNRTI resistant and multi-drug resistant human immunodeficiency virus. Antiviral. Chem. Chemother. 2000, 11, 135-140.
-
(2000)
Antiviral. Chem. Chemother.
, vol.11
, pp. 135-140
-
-
Uckun, F.M.1
Mao, C.2
Pendergrass, S.3
Maher, D.4
Zhu, D.5
Tuel-Ahlgren, L.6
Venkatachalam, T.K.7
-
8
-
-
0033590276
-
N-[2-(2-Thiophene)ethyl]-N′-[2-(5-bromopyridyl)]-thiourea as a potent inhibitor of NNI-resistant and multi-drug resistant human immunodeficiency virus-1
-
Uckun, F. M.; Pendergrass, S.; Maher, D.; Zhu, D.; Tuel-Ahlgren, L.; Mao, C.; Venkatachalam, T. K. N-[2-(2-Thiophene)ethyl]-N′-[2-(5-bromopyridyl)] -thiourea as a potent inhibitor of NNI-resistant and multi-drug resistant human immunodeficiency virus-1. Bioorg. Med. Chem. Lett. 1999, 9, 3411-3416.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 3411-3416
-
-
Uckun, F.M.1
Pendergrass, S.2
Maher, D.3
Zhu, D.4
Tuel-Ahlgren, L.5
Mao, C.6
Venkatachalam, T.K.7
-
9
-
-
0032537520
-
5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series
-
Vig, R.; Mao, C.; Venkatachalam, T. K.; Tuel-Ahlgren, L.; Sudbeck, E. A.; Uckun, F. M. 5-Alkyl-2-[(methylthiomethyl)thio]-6-[(benzyl)-pyrimidin-4-(1H)- ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series. Bioorg. Med. Chem. Lett. 1998, 8, 1461-1466.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1461-1466
-
-
Vig, R.1
Mao, C.2
Venkatachalam, T.K.3
Tuel-Ahlgren, L.4
Sudbeck, E.A.5
Uckun, F.M.6
-
10
-
-
3543052950
-
Synthesis of β-fluorophenethyl halopyridyl thiourea compounds as non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Venkatachalam, T. K.; Uckun, F. M. Synthesis of β-fluorophenethyl halopyridyl thiourea compounds as non-nucleoside inhibitors of HIV-1 reverse transcriptase. Synth. Commun. 2004, 34, 2462-2472.
-
(2004)
Synth. Commun.
, vol.34
, pp. 2462-2472
-
-
Venkatachalam, T.K.1
Uckun, F.M.2
-
11
-
-
3543147840
-
Regiospecific synthesis of 5-halo-substituted thiophene pyridyl thiourea compounds as non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Venkatachalam, T. K.; Uckun, F. M. Regiospecific synthesis of 5-halo-substituted thiophene pyridyl thiourea compounds as non-nucleoside inhibitors of HIV-1 reverse transcriptase. Synth. Commun. 2004, 34, 1-11.
-
(2004)
Synth. Commun.
, vol.34
, pp. 1-11
-
-
Venkatachalam, T.K.1
Uckun, F.M.2
-
12
-
-
0037655091
-
Introduction of carbohydrate moiety into the structure of thiourea compounds targeting HIV-1 reverse transcriptase
-
Mallikarjun, P.; Venkatachalam, T. K.; Uckun, F. M. Introduction of carbohydrate moiety into the structure of thiourea compounds targeting HIV-1 reverse transcriptase. Synth. Commun. 2003, 33, 1185-1193.
-
(2003)
Synth. Commun.
, vol.33
, pp. 1185-1193
-
-
Mallikarjun, P.1
Venkatachalam, T.K.2
Uckun, F.M.3
-
13
-
-
2342502598
-
Effect of stereo and regiochemistry towards wild and multidrug resistant HIV-1 virus: Viral potency of chiral PETT derivatives
-
Venkatachalam, T. K.; Mao, C.; Uckun, F. M. Effect of stereo and regiochemistry towards wild and multidrug resistant HIV-1 virus: Viral potency of chiral PETT derivatives. Biochem. Pharmacol. 2004, 67, 1933-1946.
-
(2004)
Biochem. Pharmacol.
, vol.67
, pp. 1933-1946
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.M.3
-
14
-
-
3042836102
-
Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds
-
Venkatachalam, T. K.; Mao, C.; Uckun, F. M. Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds. Bioorg. Med. Chem. 2004, 12, 4275-4284.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 4275-4284
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.M.3
-
15
-
-
0035197888
-
Stereochemistry as a major determinant of the anti-HIV activity of chiral naphthyl thiourea compounds
-
Venkatachalam, T. K.; Mao, C.; Uckun, F. M. Stereochemistry as a major determinant of the anti-HIV activity of chiral naphthyl thiourea compounds. Antivir. Chem. Chemother. 2001, 12, 213-221.
-
(2001)
Antivir. Chem. Chemother.
, vol.12
, pp. 213-221
-
-
Venkatachalam, T.K.1
Mao, C.2
Uckun, F.M.3
-
16
-
-
0033818253
-
Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Venkatachalam, T. K.; Sudbeck, E. A.; Mao, C.; Uckun, F. M. Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as non-nucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett. 2000, 10, 2071-2074.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2071-2074
-
-
Venkatachalam, T.K.1
Sudbeck, E.A.2
Mao, C.3
Uckun, F.M.4
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