(Q42537190)

English

5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series

scientific article published on June 1998

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

author name string

Vig R

1

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

Mao C

2

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

Venkatachalam TK

3

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

Tuel-Ahlgren L

4

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

Sudbeck EA

5

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

Uckun FM

6

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

language of work or name

0 references

publication date

1 June 1998

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

Bioorganic & Medicinal Chemistry Letters

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

8

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Europe PubMed Central

PubMed publication ID

1 November 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

1461-1466

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

The molecular biology of human immunodeficiency virus type 1 infection

1 reference

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Molecular targets for AIDS therapy

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Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives

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A new class of HIV-1-specific 6-substituted acyclouridine derivatives: synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)

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Synthesis and anti-HIV activity of novel N-1 side chain-modified analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT).

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Synthesis and potent anti-HIV-1 activity of novel 6-benzyluracil analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine

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Highly potent and selective inhibition of HIV-1 replication by 6-phenylthiouracil derivatives

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Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs

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Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs

1 reference

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The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase

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Synthesis and anti-HIV-1 activity of novel 2,3-dihydro-7H-thiazolo[3,2-a]pyrimidin-7-ones

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Dihydro(alkylthio)(naphthylmethyl)oxopyrimidines: novel non-nucleoside reverse transcriptase inhibitors of the S-DABO series

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Anti-HIV active naphthyl analogues of HEPT and DABO.

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Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor

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High resolution structures of HIV-1 RT from four RT-inhibitor complexes

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Structure of HIV-1 reverse transcriptase in a complex with the non-nucleoside inhibitor alpha-APA R 95845 at 2.8 A resolution

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Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors

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Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance

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Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors

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Scintillation proximity assay

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Inhibition of HIV replication by pokeweed antiviral protein targeted to CD4+ cells by monoclonal antibodies

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Anti-human immunodeficiency virus type 1 activity of an anti-CD4 immunoconjugate containing pokeweed antiviral protein

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Identifiers

10.1016/S0960-894X(98)00250-9

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 November 2017

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