Synthesis and biological properties of amino acid amide ligand-based pyridinioalkanoyl thioesters as anti-HIV agents (Q40745504)

23 September 2017

title

Synthesis and biological properties of amino acid amide ligand-based pyridinioalkanoyl thioesters as anti-HIV agents (English)

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23 September 2017

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2

Atul Goel

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23 September 2017

5

Judy A Mikovits

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23 September 2017

Yongsheng Song

1

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23 September 2017

Venkatesha Basrur

3

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23 September 2017

Paula E A Roberts

4

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23 September 2017

John K Inman

6

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23 September 2017

Jim A Turpin

7

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23 September 2017

William G Rice

8

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23 September 2017

Ettore Appella

9

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23 September 2017

language of work or name

English

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publication date

1 May 2002

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Bioorganic & Medicinal Chemistry

23 September 2017

published in

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23 September 2017

volume

10

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23 September 2017

issue

5

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23 September 2017

page(s)

1263-1273

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Clinical correlates of in vitro HIV-1 resistance ot zidovudine. Results of the Multicentre Canadian AZT Trial

23 September 2017

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Potential metal-binding domains in nucleic acid binding proteins

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Genetic analysis of the zinc finger in the Moloney murine leukemia virus nucleocapsid domain: replacement of zinc-coordinating residues with other zinc-coordinating residues yields noninfectious particles containing genomic RNA

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Anti-HIV agents that selectively target retroviral nucleocapsid protein zinc fingers without affecting cellular zinc finger proteins

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Reactivity of the HIV-1 nucleocapsid protein p7 zinc finger domains from the perspective of density-functional theory

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2,2'-Dithiobisbenzamides derived from alpha-, beta- and gamma-amino acids possessing anti-HIV activities: synthesis and structure-activity relationship

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The human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein zinc ejection activity of disulfide benzamides and benzisothiazolones: correlation with anti-HIV and virucidal activities

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Biophysical characterization of zinc ejection from HIV nucleocapsid protein by anti-HIV 2,2'-dithiobis[benzamides] and benzisothiazolones

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Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein.

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Synthesis and biological properties of novel pyridinioalkanoyl thiolesters (PATE) as anti-HIV-1 agents that target the viral nucleocapsid protein zinc fingers.

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Inactivation of HIV-1 nucleocapsid protein P7 by pyridinioalkanoyl thioesters. Characterization of reaction products and proposed mechanism of action.

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Chemical synthesis of phosphorylated peptides of the carboxy-terminal domain of human p53 by a segment condensation method

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Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins

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7 January 2021

Inhibitors of human immunodeficiency virus type 1 zinc fingers prevent normal processing of gag precursors and result in the release of noninfectious virus particles

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Identifiers

DOI

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23 September 2017

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