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Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides.
Liu, Xing-Hai; Shi, Yan-Xia; Ma, Yi; Zhang, Chuan-Yu; Dong, Wei-Li; Pan, Li; Wang, Bao-Lei; Li, Bao-Ju; Li, Zheng-Ming.
Affiliation
  • Liu XH; State-Key Laboratory of Elemento-Organic Chemistry, National Pesticidal Engineering Centre (Tianjin), Tianjin Key Laboratory of Pesticide Science, Nankai University, Tianjin, China.
Eur J Med Chem ; 44(7): 2782-6, 2009 Jul.
Article de En | MEDLINE | ID: mdl-19246128
A series of cyclopropanecarboxamide were prepared and tested for antifungal activity in vivo. The preliminary bioassays indicated that some compounds are comparable to the commercial fungicides. To further explore the comprehensive structure-activity relationship on the basis of fungicidal activity data, comparative molecular field analysis (CoMFA) was performed, and a statistically reliable model with good predictive power (r(2)=0.8, q(2)=0.516) was achieved. Based on the CoMFA, compound 7p was designed and synthesized, which was found to display a good antifungal activity (79.38%) as 7g and 7h.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Cyclopropanes / Relation quantitative structure-activité / Champignons / Amides / Antifongiques Type d'étude: Prognostic_studies Langue: En Journal: Eur J Med Chem Année: 2009 Type de document: Article Pays d'affiliation: Chine Pays de publication: France

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Cyclopropanes / Relation quantitative structure-activité / Champignons / Amides / Antifongiques Type d'étude: Prognostic_studies Langue: En Journal: Eur J Med Chem Année: 2009 Type de document: Article Pays d'affiliation: Chine Pays de publication: France