| Literature DB >> 30151611 |
Yun-Shan Fang1,2, Ming-Hui Yang3, Le Cai4, Jia-Peng Wang1, Tian-Peng Yin1, Jing Yu1, Zhong-Tao Ding5.
Abstract
Two new phenylpropanoids, retusiusines A (1) and B (2), and a pair of new phenylpropyl enantiomers, (±)-retusiusine C (3a and 3b), together with eight known compounds, dihydroconiferyl dihydro-p-coumarate (4), methyl 3-(4-hydroxyphenyl) propionate (5), 3-(4-hydroxyphenyl)-propanoic acid (6), dihydroferulic acid (7), methyl 3-(4-methoxyphenyl) propionate (8), 3-(3,4-dimethoxyphenyl)-2-propenal (9), trans-p-coumaric acid (10) and dihydroconiferyl alcohol (11), were isolated from the tubers of Bulbophyllum retusiusculum. The absolute configurations of the new compounds were determined by calculating their electronic circular dichroism (ECD), spectra and specific optical rotations and comparing the calculated values with the experimental data. Compound 2 exhibited potent antifungal activity against Candida albicans (16 μg/mL). Compound 3 showed moderate antibacterial activity against Bacillus subtilis (64 μg/mL).Entities:
Keywords: Absolute configuration; Antibacterial activity; Antifungal activity; Bulbophyllum retusiusculum; Phenylpropanoid; Retusiusine
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Year: 2018 PMID: 30151611 DOI: 10.1007/s12272-018-1067-6
Source DB: PubMed Journal: Arch Pharm Res ISSN: 0253-6269 Impact factor: 4.946