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Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors
by
Famiglini, Valeria
, Silvestri, Romano
in
Antiretroviral agents
/ Antiretroviral drugs
/ Drug development
/ HIV
/ Human immunodeficiency virus
/ Indoles
/ Nitrogen
/ Non-nucleoside reverse transcriptase inhibitors
/ RNA-directed DNA polymerase
/ Special Issue Collection
2018
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Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors
by
Famiglini, Valeria
, Silvestri, Romano
in
Antiretroviral agents
/ Antiretroviral drugs
/ Drug development
/ HIV
/ Human immunodeficiency virus
/ Indoles
/ Nitrogen
/ Non-nucleoside reverse transcriptase inhibitors
/ RNA-directed DNA polymerase
/ Special Issue Collection
2018
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Do you wish to request the book?
Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors
by
Famiglini, Valeria
, Silvestri, Romano
in
Antiretroviral agents
/ Antiretroviral drugs
/ Drug development
/ HIV
/ Human immunodeficiency virus
/ Indoles
/ Nitrogen
/ Non-nucleoside reverse transcriptase inhibitors
/ RNA-directed DNA polymerase
/ Special Issue Collection
2018
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Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors
Journal Article
Indolylarylsulfones, a fascinating story of highly potent human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors
2018
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Overview
Indolylarylsulfones are a potent class of human immunodeficiency virus type 1 non-nucleoside reverse transcriptase inhibitors. In this review, the structure activity relationship (SAR) studies to improve the profile of sulfone L-737,126 discovered by Merck AG have been analysed with focus on introduction of the 3′,5′-dimethyl groups at the 3-phenylsulfonyl moiety, the 2-hydroxyethyl tail at the indole-2-carboxamide nitrogen, coupling of the carboxamide nitrogen with one or two glycinamide and alaninamide units, a fluorine atom at position 4 of the indole ring and correlation between configuration of the asymmetric centre and linker length. IAS derivatives look like promising drug candidates for the treatment of AIDS and related infections in combination with other antiretroviral agents.
Publisher
SAGE Publications,Sage Publications Ltd
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