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Mallopenins A–E, Antibacterial Phenolic Derivatives from the Fruits of Mallotus philippensis
Author(s) -
Sarot Cheenpracha,
Stephen G. Pyne,
Brian O. Patrick,
Raymond J. Andersen,
Wisanu Maneerat,
Surat Laphookhieo
Publication year - 2019
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.9b00182
Subject(s) - phloroglucinol , acetone , enantiomer , chemistry , absolute configuration , stereochemistry , antibacterial activity , organic chemistry , chromatography , biology , bacteria , genetics
The chromatographic separation of the components of the acetone extract of Mallotus philippensis fruits yielded five new phenolic compounds including two chalcones, 1 and 3 , a functionalized phloroglucinol, 2 , two flavanones, 4 and 5 , and six known compounds. The structures of 1 - 5 were confirmed by NMR and mass analyses. Racemic compounds 1 and 2 were separated by chiral-phase HPLC, and the absolute configuration of (+)- 1 was confirmed by X-ray diffraction studies and ECD spectroscopic data. The configurations of the enantiomers of 2 were defined by comparison of its ECD data with those of (+)- 1 . Compounds 6 and 7 exhibited significant antibacterial activities, with MIC values ranging from 3.8 to 15.5 μM.

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