Benzoylindoles
Benzoylindoles are a class of organic compounds characterized by the presence of an indole ring fused to a benzene ring, with one or more carbonyl groups attached. These molecules exhibit diverse biological activities and have been extensively studied for their potential in various therapeutic areas. Commonly, benzoylindoles are known for their antimicrobial properties, particularly against Gram-positive bacteria, due to their ability to disrupt bacterial cell wall synthesis and membrane function. Additionally, some benzoylindoles show promise as potential antifungal agents by interfering with fungal metabolism and growth processes. Due to their structural complexity and functional diversity, these compounds have attracted significant interest in the development of new antibacterial and antifungal drugs. Research into benzoylindoles continues, focusing on optimizing their chemical structure for improved efficacy and reduced side effects.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Indomethacin 1-Glycerin Ester | 71848-87-8 | C22H22ClNO6 |
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Indomethacin Acyl-b-D-glucuronide | 75523-11-4 | C25H24ClNO10 |
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Indomethacin Isopropyl Ester | 72616-25-2 | C22H22ClNO4 |
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3-(4'-Fluorobenzoyl)indole | 152807-26-6 | C15H10FNO |
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Glucametacin | 52443-21-7 | C25H27ClN2O8 |
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Indomethacin Methyl Ester | 1601-18-9 | C20H18ClNO4 |
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Methanone,(4-chlorophenyl)(7,8-dihydrocyclopenta[b]-1,3-dioxolo[4,5-f]indol-5(6H)-yl)- | 50332-13-3 | C19H14ClNO3 |
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Methanone, (2,3-diphenyl-1H-indol-1-yl)phenyl- | 5448-01-1 | C27H19NO |
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Oxametacin | 27035-30-9 | C19H17ClN2O4 |
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1H-indol-1-yl(phenyl)methanone | 1496-76-0 | C15H11NO |
Related Literature
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Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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Jialiang Yuan,Ran Dong,Yuan Li,Yang Liu,Zhuo Zheng,Yuxia Liu,Yan Sun,Benhe Zhong,Zhenguo Wu,Xiaodong Guo Chem. Commun., 2021,57, 13004-13007
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
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