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1-苯基-3-(2,4,6-三甲氧基苯基)丙-2-烯-1-酮

1-Phenyl-3-(2,4,6-trimethoxy-phen-yl)prop-2-en-1-one.

作者信息

Wu Jianzhang, Zhang Li, Wang Jing, Yang Shulin, Li Xiaokun

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2009 Oct 23;65(Pt 11):o2805. doi: 10.1107/S1600536809041877.

DOI:10.1107/S1600536809041877
PMID:21578397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2971044/
Abstract

In the title compound, C(18)H(18)O(4), a derivative of biologically active chalcones, the dihedral angle between the two rings is 7.43 (7)°. The molecule adopts an E configuration about the central olefinic bonds. In the crystal, there are no strong inter-actions between the mol-ecules.

摘要

在标题化合物C(18)H(18)O(4)中,它是具有生物活性的查耳酮衍生物,两个环之间的二面角为7.43 (7)°。分子围绕中心烯键采取E构型。在晶体中,分子之间不存在强相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ef7/2971044/90c14a74e529/e-65-o2805-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ef7/2971044/90c14a74e529/e-65-o2805-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ef7/2971044/90c14a74e529/e-65-o2805-fig1.jpg

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本文引用的文献

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(E)-1-(2-Thien-yl)-3-(3,4,5-trimethoxy-phen-yl)prop-2-en-1-one.
Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 13;65(Pt 7):o1575-6. doi: 10.1107/S1600536809021850.
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Antifungal activity, mechanism and QSAR studies on chalcones.查耳酮类化合物的抗真菌活性、作用机制及定量构效关系研究
Acta Crystallogr Sect E Struct Rep Online. 2010 Apr 24;66(Pt 5):o1156-7. doi: 10.1107/S1600536810014169.
Chem Biol Drug Des. 2009 Jul;74(1):68-79. doi: 10.1111/j.1747-0285.2009.00828.x.
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Structural antitumoral activity relationships of synthetic chalcones.合成查耳酮的结构抗肿瘤活性关系。
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