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Delavirdine
Known as:
Delavirdin
, 1-(3-((1-Methylethyl)amino)-2-pyridinyl)-4-((5-((methylsulfonyl)amino)-1H-indol-2-yl)carbonyl)piperazine
, Delavirdina
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A synthetic, non-nucleoside reverse transcriptase inhibitor. In combination with other anti-retroviral drugs, this agent has been shown to reduce HIV…
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National Institutes of Health
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Related topics
Related topics
29 relations
Acquired Immunodeficiency Syndrome
Alprazolam
Astemizole
Cisapride
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Broader (5)
Anti-HIV Agents
Antiviral Agents
Indoles
Piperazines
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Narrower (2)
Rescriptor
U-90152
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
Probing nonnucleoside inhibitor‐induced active‐site distortion in HIV‐1 reverse transcriptase by transient kinetic analyses
Qing Xia
,
Jessica A. Radzio
,
K. Anderson
,
N. Sluis-Cremer
Protein Science
2007
Corpus ID: 22085379
Nonnucleoside reverse transcriptase inhibitors (NNRTI) are a group of structurally diverse compounds that bind to a single site…
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2007
2007
Management and treatment of hepatitis C virus in patients with HIV and hepatitis C virus coinfection: A practical guide for health care professionals.
P. Cote
,
J. Baril
,
+17 authors
A. Piché
The Canadian journal of infectious diseases…
2007
Corpus ID: 41527784
Concomitant HIV and hepatitis C virus (HCV) is a common yet complex coinfection. The present document is a practical guide for…
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Highly Cited
2001
Highly Cited
2001
Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds.
T. Venkatachalam
,
E. Sudbeck
,
C. Mao
,
F. Uckun
Bioorganic & Medicinal Chemistry Letters
2001
Corpus ID: 7078073
2001
2001
Potentiation of Inhibition of Wild-Type and Mutant Human Immunodeficiency Virus Type 1 Reverse Transcriptases by Combinations of Nonnucleoside Inhibitors and d- and l-(β)-Dideoxynucleoside…
G. Maga
,
U. Hübscher
,
M. Pregnolato
,
D. Ubiali
,
G. Gosselin
,
S. Spadari
Antimicrobial Agents and Chemotherapy
2001
Corpus ID: 3049160
ABSTRACT Combinations of reverse transcriptase (RT) inhibitors are currently used in anti-human immunodeficiency virus therapy in…
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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
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
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
ACTG 260: a Randomized, Phase I-II, Dose-Ranging Trial of the Anti-Human Immunodeficiency Virus Activity of Delavirdine Monotherapy
M. Para
,
P. Meehan
,
+8 authors
W. Freimuth
Antimicrobial Agents and Chemotherapy
1999
Corpus ID: 42059658
ABSTRACT ACTG 260 was an open-label, four-arm trial designed to study the safety and anti-human immunodeficiency virus (anti-HIV…
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1999
1999
Acute Hypersensitivity with Delavirdine
G. Mills
,
J. Morgan
,
G. Hales
,
D. Smith
Antiviral Therapy
1999
Corpus ID: 21406698
Delavirdine is an antiretroviral drug now being used as part of combination antiretroviral therapy for the management of human…
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Highly Cited
1986
Highly Cited
1986
Resistance to anthrapyrazoles and anthracyclines in multidrug-resistant P388 murine leukemia cells: reversal by calcium blockers and calmodulin antagonists.
W. Klohs
,
R. Steinkampf
,
M. Havlick
,
R. Jackson
Cancer Research
1986
Corpus ID: 5933207
A series of anthrapyrazoles was examined for their cytotoxic effect on P388 cells resistant (P388R) to anthracyclines, N-[4-(9…
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