Synthesis and antiviral activities of methylenecyclopropane analogs with 6-alkoxy and 6-alkylthio substitutions that exhibit broad-spectrum antiviral activity against human herpesviruses. (Q37036545)

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scientific article published on 13 May 2013

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English	Synthesis and antiviral activities of methylenecyclopropane analogs with 6-alkoxy and 6-alkylthio substitutions that exhibit broad-spectrum antiviral activity against human herpesviruses.	scientific article published on 13 May 2013

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scholarly article

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1 March 2020

Synthesis and antiviral activities of methylenecyclopropane analogs with 6-alkoxy and 6-alkylthio substitutions that exhibit broad-spectrum antiviral activity against human herpesviruses (English)

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John D Williams

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Gloria Komazin-Meredith

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Atiyya R Khan

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Nathan B Price

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Geraldine M Jefferson

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Emma A Harden

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Caroll B Hartline

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Norton P Peet

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Terry L Bowlin

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13 May 2013

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Antimicrobial Agents and Chemotherapy

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3518-3527

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8

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1 March 2020

Synthesis and antiviral activity of certain second generation methylenecyclopropane nucleosides

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Progress in the development of new therapies for herpesvirus infections

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(Z)- and (E)-2-(1,2-dihydroxyethyl)methylenecyclopropane analogues of 2'-deoxyadenosine and 2'-deoxyguanosine. Synthesis of all stereoisomers, absolute configuration, and antiviral activity.

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Oral activity of a methylenecyclopropane analog, cyclopropavir, in animal models for cytomegalovirus infections

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Synthesis and enantioselectivity of the antiviral effects of (R,Z)-,(S,Z)-methylenecyclopropane analogues of purine nucleosides and phosphoralaninate prodrugs: influence of heterocyclic base, type of virus and host cells

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Identifiers

10.1128/AAC.00429-13

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1 March 2020

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1 March 2020

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