z-logo
Premium
Cytotoxic Withanolides from Physalis angulata L.
Author(s) -
He QingPing,
Ma Lei,
Luo JieYing,
He FuYuan,
Lou LiGuang,
Hu LiHong
Publication year - 2007
Publication title -
chemistry and biodiversity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 70
eISSN - 1612-1880
pISSN - 1612-1872
DOI - 10.1002/cbdv.200790036
Subject(s) - chemistry , cytotoxicity , stereochemistry , solanaceae , two dimensional nuclear magnetic resonance spectroscopy , dept , ic50 , physalis , cell culture , traditional medicine , hep g2 , in vitro , biochemistry , biology , medicine , gene , genetics
Four new withanolides, physagulins L–O ( 1 – 4 ), were isolated from the MeOH extract of the aerial parts of Physalis angulata L. (Solanaceae), together with seven known withanolides, compounds 5 – 11 . Their structures were determined by spectroscopic techniques, including 1 H‐, 13 C‐NMR (DEPT), and 2D‐NMR (HMBC, HMQC, 1 H, 1 H‐COSY, NOESY) experiments, as well as by HR‐MS. All eleven compounds were tested for their antiproliferative activities towards human colorectal‐carcinoma (HCT‐116) and human non‐small‐cell lung‐cancer (NCI‐H460) cells. Compound 5 exhibited the highest anticancer activity against the HCT‐116 cell line, with an IC 50 value of 1.64±0.06 μ M . Compound 9 exhibited the highest cytotoxicity towards the NCI‐H460 cell line, with an IC 50 value of 0.43±0.02 μ M ( Table 3 ).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom