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trovirdine
Known as:
1-(5-Bromo-2-pyridyl)-3-(2-(2-pyridyl)ethyl)-2-thiourea
A thiourea non-nucleoside reverse transcriptase inhibitor.
National Institutes of Health
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Pyridines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Efficacy of antiretroviral compounds against Toxoplasma gondii in vitro.
Jin-Lei Wang
,
H. Elsheikha
,
+5 authors
W. Cong
International Journal of Antimicrobial Agents
2019
Corpus ID: 201830123
2007
2007
Design, synthesis and biological evaluation of a series of thioamides as non-nucleoside reverse transcriptase inhibitors.
A. Mehanna
,
Jitendra D. Belani
,
C. Kelley
,
Luke A Pallansc
Medicinal chemistry
2007
Corpus ID: 22367027
A series of thioamides were designed as bio-isosteres to the non-nucleoside reverse transcriptase inhibitor trovirdine by…
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2003
2003
Synthesis and Anti-HIV Activity of Some Heterodimers [NRTI]-Glycyl-Succinyl-[Trovirdine Analogue] of Known HIV-1 Reverse Transcriptase Inhibitors
E. Sugeac
,
C. Fossey
,
D. Ladurée
,
S. Schmidt
,
G. Laumond
,
A. Aubertin
Journal of Enzyme Inhibition and Medicinal…
2003
Corpus ID: 23096393
Expected for their ability to inhibit HIV replication, four heterodimers with a Nucleoside Reverse Transcriptase Inhibitor (NRTI…
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2000
2000
Stereochemistry of halopyridyl and thiazolyl thiourea compounds is a major determinant of their potency as nonnucleoside inhibitors of HIV-1 reverse transcriptase.
T. Venkatachalam
,
E. Sudbeck
,
C. Mao
,
F. Uckun
Bioorganic & Medicinal Chemistry Letters
2000
Corpus ID: 24568397
2000
2000
N-[2-(4-Methylphenyl)Ethyl]-N′-[2-(5-Bromopyridyl)]-Thiourea as a Potent Inhibitor of NNRTI-Resistant and Multidrug-Resistant Human Immunodeficiency Virus Type 1
F. Uckun
,
Chen Mao
,
+4 authors
T. Venkatachalam
Antiviral Chemistry & Chemotherapy
2000
Corpus ID: 10520579
The composite non-nucleoside reverse transcriptase inhibitor (NNRTI) binding pocket model was used to study a number of thiourea…
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1999
1999
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 multidrug-resistant human immunodeficiency…
F. Uckun
,
C. Mao
,
+4 authors
T. Venkatachalam
Bioorganic & Medicinal Chemistry Letters
1999
Corpus ID: 9319754
1999
1999
N'-[2-(2-thiophene)ethyl]-N'-[2-(5-bromopyridyl)] thiourea as a potent inhibitor of NNI-resistant and multidrug-resistant human immunodeficiency virus-1.
F. Uckun
,
S. Pendergrass
,
+4 authors
T. Venkatachalam
Bioorganic & Medicinal Chemistry Letters
1999
Corpus ID: 20711884
1999
1999
Novel derivatives of phenethyl-5-bromopyridylthiourea and dihydroalkoxybenzyloxopyrimidine are dual-function spermicides with potent anti-human immunodeficiency virus activity.
O. D’cruz
,
F. Uckun
Biology of Reproduction
1999
Corpus ID: 41053270
Sexually active women represent the fastest growing HIV/AIDS (human immunodeficiency virus/acquired immunodeficiency syndrome…
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Highly Cited
1998
Highly Cited
1998
Structure-based design of N-[2-(1-piperidinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1…
C. Mao
,
R. Vig
,
T. Venkatachalam
,
E. Sudbeck
,
F. Uckun
Bioorganic & Medicinal Chemistry Letters
1998
Corpus ID: 10858921
1995
1995
Inhibition of human immunodeficiency virus type 1 wild-type and mutant reverse transcriptases by the phenyl ethyl thiazolyl thiourea derivatives trovirdine and MSC-127.
Hong Zhang
,
L. Vrang
,
+4 authors
Bo Öberg
Antiviral Research
1995
Corpus ID: 25617886
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