Phenolic compounds from Glycyrrhiza pallidiflora Maxim. and their cytotoxic activity Full article
Journal |
Natural Product Research
ISSN: 1478-6419 , E-ISSN: 1478-6427 |
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Output data | Year: 2017, Volume: 31, Number: 4, Pages: 445-452 Pages count : DOI: 10.1080/14786419.2016.1188094 | ||||||
Tags | Glycyrrhiza pallidiflora; flavonoids; pterocarpans; isoflavonoids; cytotoxic activity | ||||||
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Abstract:
Twenty-one phenolic compounds (1-21) including dihydrocinnamic acid, isoflavonoids, flavonoids, coumestans, pterocarpans, chalcones, isoflavan and isoflaven, were isolated from the roots of Glycyrrhiza pallidiflora Maxim. Phloretinic acid (1), chrysin (6), 9-methoxycoumestan (8), isoglycyrol (9), 6"-O-acetylanonin (19) and 6"-O-acetylwistin (21) were isolated from G. pallidiflora for the first time. Isoflavonoid acetylglycosides 19, 21 might be artefacts that could be produced during the EtOAc fractionation process of whole extract. Compounds 2-4, 10, 11, 19 and 21 were evaluated for their cytotoxic activity with respect to model cancer cell lines (CEM-13, MT4, U-937) using the conventional MTT assays. Isoflavonoid calycosin (4) showed the best potency against human T-cell leukaemia cells MT-4 (CTD50, 2.9 mu M). Pterocarpans medicarpin (10) and homopterocarpin (11) exhibit anticancer activity in micromolar range with selectivity on the human monocyte cells U-937. The isoflavan (3R)-vestitol (16) was highly selective on the lymphoblastoid leukaemia cells CEM-13 and was more active than the drug doxorubicin [GRAPHICS] .
Cite:
Shults E.E.
, Shakirov M.M.
, Pokrovsky M.A.
, Petrova T.N.
, Pokrovsky A.G.
, Gorovoy P.G.
Phenolic compounds from Glycyrrhiza pallidiflora Maxim. and their cytotoxic activity
Natural Product Research. 2017. V.31. N4. P.445-452. DOI: 10.1080/14786419.2016.1188094 WOS Scopus РИНЦ
Phenolic compounds from Glycyrrhiza pallidiflora Maxim. and their cytotoxic activity
Natural Product Research. 2017. V.31. N4. P.445-452. DOI: 10.1080/14786419.2016.1188094 WOS Scopus РИНЦ
Dates:
Published online: | May 22, 2016 |
Published print: | Feb 16, 2017 |
Identifiers:
Web of science | WOS:000392626400010 |
Scopus | 2-s2.0-84969816543 |
Elibrary | 28464893 |
OpenAlex | W2399045633 |