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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom