(Q28377075)

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Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2' substituents

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Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2' substituents (English)

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author name string

M Patel

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1

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J D Rodgers

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2

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R J McHugh

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3

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B L Johnson

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4

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B C Cordova

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5

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R M Klabe

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6

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L T Bacheler

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7

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S Erickson-Viitanen

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8

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S S Ko

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9

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language of work or name

English

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publication date

15 November 1999

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published in

Bioorganic & Medicinal Chemistry Letters

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volume

9

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issue

22

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page(s)

3217-20

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cites work

Potent cyclic urea HIV protease inhibitors with 3-aminoindazole P2/P2' groups

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https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900564-8

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7 January 2021

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Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors

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https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900564-8

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7 January 2021

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Nonsymmetric P2/P2' cyclic urea HIV protease inhibitors. Structure-activity relationship, bioavailability, and resistance profile of monoindazole-substituted P2 analogues

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7 January 2021

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Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

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Synthetic Transformations of Vinyl and Aryl Triflates

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7 January 2021

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Cyclic urea amides: HIV-1 protease inhibitors with low nanomolar potency against both wild type and protease inhibitor resistant mutants of HIV

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https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900564-8

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7 January 2021

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Potency and selectivity of inhibition of human immunodeficiency virus protease by a small nonpeptide cyclic urea, DMP 323

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7 January 2021

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10.1016/S0960-894X(99)00564-8

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PubMed publication ID

10576691

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(Q28377075)

Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2' substituents

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