New Anthraquinone Derivatives as Inhibitors of the HIV-1 Reverse Transcriptase-Associated Ribonuclease H Function (Q58196901)

Angela Corona

2

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Enzo Tramontano

Enzo Tramontano

5

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Luca Zinzula

3

Luca Zinzula

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Tatyana Kharlamova

4

The structural biology of HIV-1: mechanistic and therapeutic insights

Tatyana Kharlamova

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publication date

2012

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published in

Chemotherapy

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volume

58

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issue

4

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page(s)

299-307

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cites work

1 reference

HIV-1 Reverse Transcriptase Still Remains a New Drug Target: Structure, Function, Classical Inhibitors, and New Inhibitors with Innovative Mechanisms of Actions.

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6-[1-(4-Fluorophenyl)methyl-1H-pyrrol-2-yl)]-2,4-dioxo-5-hexenoic acid ethyl ester a novel diketo acid derivative which selectively inhibits the HIV-1 viral replication in cell culture and the ribonuclease H activity in vitro

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Development of a series of 3-hydroxyquinolin-2(1H)-ones as selective inhibitors of HIV-1 reverse transcriptase associated RNase H activity

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HIV-1 Reverse Transcriptase Structure with RNase H Inhibitor Dihydroxy Benzoyl Naphthyl Hydrazone Bound at a Novel Site

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