Literature DB >> 26140544

Scillapersicene: a new homoisoflavonoid with cytotoxic activity from the bulbs of Scilla persica HAUSSKN.

Salar Hafez Ghoran1, Soodabeh Saeidnia2, Esmaeil Babaei3, Fumiyuki Kiuchi4, Hidayat Hussain5.   

Abstract

The phytochemical investigation of Scilla persica HAUSSKN bulbs led to the isolation of a novel homoisoflavonoid that named Scillapersicene (1) and identified as 3-(3',4'-dihydroxybenzylidene)-8-hydroxy-5,7-dimethoxychroman-4-one along with five known homoisoflavonoids 2-6, whose structures were elucidated using HRFAB-MS, 1D and 2D NMR spectroscopic data. The known compounds were identified as 3-(3',4'-dihydroxybenzyl)-5,8-dihydroxy-7-methoxychroman-4-one (2), 3,9-dihydro-autumnalin (3), autumnalin (4), 3-(3',4'-dihydroxybenzylidene)-5,8-dihydroxy-7-methoxychroman-4-one (5) and scillapersicone (6). All compounds obtained, expect 2 and 4, showed strong cytotoxic activity against AGS cell line. The toxicity on AGS cell line was measured by 1, 3, 5 and 6 with IC50 values of 8.4, 30.5, 10.7 and 24.2 μM, respectively. In addition, the physico-chemical properties of these natural compounds were optimised using density functional method (B3LYP) with standard 6-311+G* basis set. These natural products have low-energy gaps between the first ionisation potentials and highest occupied molecular orbital. In conclusion, the low-energy gap could cause reason for cytotoxic activity of homoisoflavonoids.

Entities:  

Keywords:  AGS; B3LYP; Liliaceae; Scilla persica; Scillapersicene; cytotoxic activity; homoisoflavonoid

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Year:  2015        PMID: 26140544     DOI: 10.1080/14786419.2015.1054286

Source DB:  PubMed          Journal:  Nat Prod Res        ISSN: 1478-6419            Impact factor:   2.861


  3 in total

1.  Anti-Inflammatory Properties of Bellevalia saviczii Root Extract and Its Isolated Homoisoflavonoid (Dracol) Are Mediated by Modification on Calcium Signaling.

Authors:  Monica Savio; Mohammed Farhad Ibrahim; Chiara Scarlata; Matteo Orgiu; Giuseppe Accardo; Abdullah Shakur Sardar; Francesco Moccia; Lucia Anna Stivala; Gloria Brusotti
Journal:  Molecules       Date:  2019-09-17       Impact factor: 4.411

2.  Synthesis of Natural Homoisoflavonoids Having Either 5,7-Dihydroxy-6-methoxy or 7-Hydroxy-5,6-dimethoxy Groups.

Authors:  Hyungjun Lee; Yue Yuan; Inmoo Rhee; Timothy W Corson; Seung-Yong Seo
Journal:  Molecules       Date:  2016-08-13       Impact factor: 4.411

Review 3.  A Comprehensive Review on Chemotaxonomic and Phytochemical Aspects of Homoisoflavonoids, as Rare Flavonoid Derivatives.

Authors:  Javad Mottaghipisheh; Hermann Stuppner
Journal:  Int J Mol Sci       Date:  2021-03-08       Impact factor: 5.923

  3 in total

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