Searching for the Stereoisomer of 7,7′-Epoxylignan Showing the Most Potent Antifungal Activity and Finding the 3-(Trifluoromethyl)-4-hydroxy-3′-fluoro Derivative to Have the Highest Activity
Author:
Affiliation:
1. Graduate School of Agriculture, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime 790-8566, Japan
2. Integrated Center for Sciences, Tarumi Station, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime 790-8566, Japan
Funder
Sumitomo Foundation
Publisher
American Chemical Society (ACS)
Subject
Plant Science,Agricultural and Biological Sciences (miscellaneous),Agronomy and Crop Science,Food Science
Link
https://pubs.acs.org/doi/pdf/10.1021/acsagscitech.1c00117
Reference44 articles.
1. Quantitative Structure–Activity Relationship Analysis of Antifungal (+)-Dihydroguaiaretic Acid Using 7-Phenyl Derivatives
2. A registry of the natural lignans
3. Cytotoxic Activity of Dietary Lignan and Its Derivatives: Structure–Cytotoxic Activity Relationship of Dihydroguaiaretic Acid
4. Effect of the structure of dietary epoxylignan on its cytotoxic activity: relationship between the structure and the activity of 7,7′-epoxylignan and the introduction of apoptosis by caspase 3/7
5. Enantioselective syntheses of both enantiomers of 9′-dehydroxyimperanene and 7,8-dihydro-9′-dehydroxyimperanene and the comparison of biological activity between 9-norlignans and dihydroguaiaretic acids
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