Tetrahydrofuran, tetrahydropyran, triazoles and related heterocyclic derivatives as HIV protease inhibitors. - Test2 - elhamkhani - TriplyDB

Tetrahydrofuran, tetrahydropyran, triazoles and related heterocyclic derivatives as HIV protease inhibitors.

Tetrahydrofuran, tetrahydropyran, triazoles and related heterocyclic derivatives as HIV protease inhibitors.

http://www.wikidata.org/entity/Q37909409

about

A fission yeast cell-based system for multidrug resistant HIV-1 proteases.Asymmetric organocatalytic methods for the synthesis of tetrahydropyrans and their application in total synthesis.Molecular basis and potential activity of HIV-1 reverse transcriptase toward trimethylamine-based compounds.Straightforward and highly diastereoselective synthesis of 2,2-di-substituted perhydrofuro[2,3-b]pyran (and furan) derivatives promoted by BiCl3.Diastereoselective synthesis of 3-acetoxy-4-(3-aryloxiran-2-yl)azetidin-2-ones and their transformation into 3,4-oxolane-fused bicyclic β-lactams.A neighboring group participation strategy: direct and highly diastereoselective synthesis of 2-substituted and 2,2-bisubstituted perhydrofuro[2,3-b]pyran derivatives.Lewis Acid Mediated Cyclizations: Diastereoselective Synthesis of Six- to Eight-Membered Substituted Cyclic Ethers.

P2860

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P2860

Tetrahydrofuran, tetrahydropyran, triazoles and related heterocyclic derivatives as HIV protease inhibitors.

http://www.wikidata.org/entity/Q37909409

description

article científic

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article scientifique

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articol științific

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articolo scientifico

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artigo científico

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artigo científico

@pt

artigo científico

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artikel ilmiah

@id

artikull shkencor

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artículo científico

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name

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@en

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@nl

type

label

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@en

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@nl

prefLabel

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@en

Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@nl

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Future Medicinal Chemistry

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Tetrahydrofuran, tetrahydropyr ...... es as HIV protease inhibitors.

@en

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Arun K Ghosh

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David D Anderson

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P2860

Discovery of HIV-1 protease inhibitors with picomolar affinities incorporating N-aryl-oxazolidinone-5-carboxamides as novel P2 ligands

Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2‘ Ligands in Pseudosymmetric Dipeptide Isosteres

Potent New Antiviral Compound Shows Similar Inhibition and Structural Interactions with Drug Resistant Mutants and Wild Type HIV-1 Protease †

Structure-guided design of C2-symmetric HIV-1 protease inhibitors based on a pyrrolidine scaffold

Structural and kinetic analysis of pyrrolidine-based inhibitors of the drug-resistant Ile84Val mutant of HIV-1 protease

Targeting the open-flap conformation of HIV-1 protease with pyrrolidine-based inhibitors

Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein−Ligand X-ray Studies †

Potent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein–ligand X-ray studies

Design of HIV-1 Protease Inhibitors with Pyrrolidinones and Oxazolidinones as Novel P1′-Ligands To Enhance Backbone-Binding Interactions with Protease: Synthesis, Biological Evaluation, and Protein−Ligand X-ray Studies ∞

Small-sized human immunodeficiency virus type-1 protease inhibitors containing allophenylnorstatine to explore the S2' pocket

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1181-1197

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scholarly article

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10.4155/FMC.11.68

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9

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3

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2011-07-01T00:00:00Z

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51537616

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21806380

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3164575

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