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Molecules
Volume 16
Issue 11
10.3390/molecules16119739
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Open AccessArticle

Diversity Oriented Design of Various Benzophenone Derivatives and Their in Vitro Antifungal and Antibacterial Activities

by , , , , , and
Dequn Sun
*
Marine College, Shandong University, Weihai Wenhua West Road, No.180, Weihai 264209, China
*
Author to whom correspondence should be addressed.
Molecules 2011, 16(11), 9739-9754; https://doi.org/10.3390/molecules16119739
Received: 3 October 2011 / Revised: 9 November 2011 / Accepted: 14 November 2011 / Published: 23 November 2011
(This article belongs to the Section Medicinal Chemistry)
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Abstract

A series of new substituted benzophenone derivatives was designed, synthesized and screened for their antifungal and antibacterial activities. The bioassays indicated that most of the synthesized compounds showed some antifungal activity against the tested phytopathogenic fungi, but lower antibacterial activities towards the five vibrios isolated from marine sources. The preliminary structure activity relationship (SAR) of the compounds was also discussed. View Full-Text
Keywords: benzophenone derivatives; bioactivity; phytopathogenic fungi; vibrio benzophenone derivatives; bioactivity; phytopathogenic fungi; vibrio
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MDPI and ACS Style

Sun, L.; Wu, J.; Luo, M.; Wang, X.; Pan, M.; Gou, Z.; Sun, D. Diversity Oriented Design of Various Benzophenone Derivatives and Their in Vitro Antifungal and Antibacterial Activities. Molecules 2011, 16, 9739-9754. https://doi.org/10.3390/molecules16119739

AMA Style

Sun L, Wu J, Luo M, Wang X, Pan M, Gou Z, Sun D. Diversity Oriented Design of Various Benzophenone Derivatives and Their in Vitro Antifungal and Antibacterial Activities. Molecules. 2011; 16(11):9739-9754. https://doi.org/10.3390/molecules16119739

Chicago/Turabian Style

Sun, Li; Wu, Jie; Luo, Min; Wang, Xiaoli; Pan, Man; Gou, Zhaopin; Sun, Dequn. 2011. "Diversity Oriented Design of Various Benzophenone Derivatives and Their in Vitro Antifungal and Antibacterial Activities" Molecules 16, no. 11: 9739-9754. https://doi.org/10.3390/molecules16119739

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