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carbovir
Known as:
(+ -)-Carbovir
, 2',3'-didehydro-2',3'-dideoxyguanosine
A nucleoside reverse transcriptase inhibitor analog of guanosine. Carbovir decreases HIV viral loads, retards or prevents the damage to the immune…
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National Institutes of Health
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Related topics
Related topics
3 relations
Broader (2)
Anti-HIV Agents
Dideoxynucleosides
Narrower (1)
NSC 614846
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Molecular Mechanism by Which the K70E Mutation in Human Immunodeficiency Virus Type 1 Reverse Transcriptase Confers Resistance to Nucleoside Reverse Transcriptase Inhibitors
N. Sluis-Cremer
,
C. Sheen
,
Shannon Zelina
,
Pedro S Argoti Torres
,
U. Parikh
,
J. Mellors
Antimicrobial Agents and Chemotherapy
2006
Corpus ID: 24946144
ABSTRACT The K70E mutation in human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) has become more prevalent in…
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Highly Cited
2005
Highly Cited
2005
A combination of decreased NRTI incorporation and decreased excision determines the resistance profile of HIV-1 K65R RT
K. White
,
N. Margot
,
+7 authors
Michael D. Miller
AIDS (London)
2005
Corpus ID: 2137967
Objective:To determine the mechanisms of resistance of K65R mutant reverse transcriptase (RT) to the currently approved…
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2001
2001
Antiviral Activity of Cyclosaligenyl Prodrugs of Acyclovir, Carbovir and Abacavir
J. Balzarini
,
F. Haller-Meier
,
E. De Clercq
,
C. Meier
Antiviral Chemistry & Chemotherapy
2001
Corpus ID: 22858760
The cyclosaligenyl (cycloSal) derivatives of the monophosphates of three acyclic or carbocyclic guanosine analogues, for example…
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2000
2000
A novel, one-pot ring expansion of cyclobutanones. Syntheses of carbovir and aristeromycin.
Brian Brown
,
L. Hegedus
Journal of Organic Chemistry
2000
Corpus ID: 19288928
A novel, one-pot ring-expansion procedure was developed using Me3S(O)I, NaH, and Sc(OTf)3. The scope and limitations were briefly…
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1999
1999
Stereoselective Synthesis of 4'-α-Alkylcarbovir Derivatives Based on an Asymmetric Synthesis or Chemoenzymatic Procedure
Keisuke Kato
,
H. Suzuki
,
+4 authors
H. Akita
1999
Corpus ID: 59145128
Stereoselective synthesis of 4'-α-alkylcarbovir derivatives 4 was described based on asymmetric synthesis or a chemoenzymatic…
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1994
1994
Enzyme-catalysed kinetic resolution of 4-endo-hydroxy-2-oxabicyclo[3.3.0]oct-7-en-3-one and employment of the pure enantiomers for the synthesis of anti-viral and hypocholestemic agents.
R. Mackeith
,
R. Mccague
,
H. Olivo
,
S. Roberts
,
S. Taylor
,
H. Xiong
Bioorganic & Medicinal Chemistry
1994
Corpus ID: 36233840
1992
1992
DNA chain termination activity and inhibition of human immunodeficiency virus reverse transcriptase by carbocyclic 2',3'-didehydro-2',3'-dideoxyguanosine triphosphate.
D. Orr
,
H. T. Figueiredo
,
C. Mo
,
C. Penn
,
J. Cameron
Journal of Biological Chemistry
1992
Corpus ID: 21013179
Highly Cited
1992
Highly Cited
1992
Synthesis and anti-HIV activity of 9-[c-4,t-5-bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine.
N. Katagiri
,
M. Nomura
,
H. Satō
,
C. Kaneko
,
K. Yusa
,
T. Tsuruo
Journal of Medicinal Chemistry
1992
Corpus ID: 45109467
The synthesis and in vitro anti-HIV activity of two new racemic nucleoside analogues are described; namely, 9-[c-4,t-5-bis…
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Highly Cited
1991
Highly Cited
1991
Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases alpha, beta, and gamma by the 5'-triphosphates of carbovir, 3'-azido-3'-deoxythymidine…
W. Parker
,
E L White
,
+6 authors
W. M. Shannon
Journal of Biological Chemistry
1991
Corpus ID: 24847636
1990
1990
Metabolism of the carbocyclic nucleoside analogue carbovir, an inhibitor of human immunodeficiency virus, in human lymphoid cells.
L. L. Bondoc
,
W. M. Shannon
,
J. Secrist
,
R. Vince
,
A. Fridland
Biochemistry
1990
Corpus ID: 29912269
Carbovir (CBV) is a highly selective carbocyclic nucleoside inhibitor of HIV replication in human lymphocytes and is potentially…
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