The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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Imidazopyridine compounds inhibit mycobacterial growth by depleting ATP levels.Synthesis of Compounds of the Pyrimidine Series Based on the Reactions of 3-Arylmethylidenefuran-2(3H)-ones with N,N-Binucleophilic Reagents.

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The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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name

The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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P1476

The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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Aaron Korkegian

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Edison S Zuniga

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Erik J Hembre

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Guillermo Cortez

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Jeffrey Cramer

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Joshua Odingo

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Kallolmay Biswas

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Naresh Kumar

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Paul L Ornstein

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Philip A Hipskind

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Structure-Guided Lead Optimization of Triazolopyrimidine-Ring Substituents Identifies Potent Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitors with Clinical Candidate Potential

Identification of novel imidazo[1,2-a]pyridine inhibitors targeting M. tuberculosis QcrB

A dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosis

Fueling open-source drug discovery: 177 small-molecule leads against tuberculosis.

Advent of Imidazo[1,2-a]pyridine-3-carboxamides with Potent Multi- and Extended Drug Resistant Antituberculosis Activity

Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice

Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization.

Identification of a metabolically stable triazolopyrimidine-based dihydroorotate dehydrogenase inhibitor with antimalarial activity in mice

Triazolopyrimidine compounds containing first-row transition metals and their activity against the neglected infectious Chagas disease and leishmaniasis.

Essramycin: a first triazolopyrimidine antibiotic isolated from nature.

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scholarly article

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10.1016/J.BMC.2017.05.030

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English

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2017-05-19T00:00:00Z

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The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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P2860

P2860

The synthesis and evaluation of triazolopyrimidines as anti-tubercular agents.

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