Efficient synthesis of novel 3-aryl-5-(4-chloro-2-morpholinothiazol-5-yl)-4,5-dihydro-1H-pyrazoles and their antifungal activity alone and in combination with commercial antifungal agents.

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Hybrid Molecules Containing a 7-Chloro-4-aminoquinoline Nucleus and a Substituted 2-Pyrazoline with Antiproliferative and Antifungal Activity.In Vitro Activities of Novel Azole Compounds ATTAF-1 and ATTAF-2 against Fluconazole-Susceptible and -Resistant Isolates of Candida Species.

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P2860

Efficient synthesis of novel 3-aryl-5-(4-chloro-2-morpholinothiazol-5-yl)-4,5-dihydro-1H-pyrazoles and their antifungal activity alone and in combination with commercial antifungal agents.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Efficient synthesis of novel 3 ...... commercial antifungal agents.

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Efficient synthesis of novel 3 ...... commercial antifungal agents.

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Efficient synthesis of novel 3 ...... commercial antifungal agents.

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Efficient synthesis of novel 3 ...... commercial antifungal agents.

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Efficient synthesis of novel 3 ...... commercial antifungal agents.

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Efficient synthesis of novel 3 ...... commercial antifungal agents.

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P1476

Efficient synthesis of novel 3 ...... h commercial antifungal agents

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P2093

Braulio Insuasty

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María Victoria Rodríguez

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Rodrigo Abonia

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Susana A Zacchino

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P2860

High-throughput synergy screening identifies microbial metabolites as combination agents for the treatment of fungal infections

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Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies

Potent in vitro synergism of fluconazole and berberine chloride against clinical isolates of Candida albicans resistant to fluconazole.

Discovery and optimization of a series of 2-aryl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazoles as novel anticancer agents.

Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl-thiazoles analogues as potent and orally bioavailable anticancer agents

Overview of the chemistry of 2-thiazolines.

Discovery of 4-substituted methoxybenzoyl-aryl-thiazole as novel anticancer agents: synthesis, biological evaluation, and structure-activity relationships

2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization.

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566-575

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scholarly article

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10.1002/ARDP.201400084

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347

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Jairo Quiroga

Maximiliano Sortino

Juan Ramírez

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2014-06-04T00:00:00Z

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262845053

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Efficient synthesis of novel 3-aryl-5-(4-chloro-2-morpholinothiazol-5-yl)-4,5-dihydro-1H-pyrazoles and their antifungal activity alone and in combination with commercial antifungal agents.

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P2860

P2860

Efficient synthesis of novel 3-aryl-5-(4-chloro-2-morpholinothiazol-5-yl)-4,5-dihydro-1H-pyrazoles and their antifungal activity alone and in combination with commercial antifungal agents.

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