Answers are grounded in this paper and cite their sources.
Phytochemical investigation of Dichanthium annulatum (Forrsk), herbs revealed the isolation and identification of two pairs of lignoflavone derivatives stereoisomers; an epimers of tricin 4`-O-(threo-βguaiacylglyceryl) ether (Salcolin A) and tricin 4`-O-(erythro-β-guaiacylglyceryl) ether (Salcolin B) (1) and an epimer of tricin 4`-O-[threo-β-guaiacyl-(7``-O-methyl-9``-O-acetyl)-glyceryl] ether and tricin 4`-O-[erythro-βguaiacyl-(7``-O-methyl-9``-O-acetyl)-glyceryl] ether (2), one flavone; tricin (3), two flavone glycosides; tricin 7-O-β-D-glucopyranoside (4) and tricin 7-O-neohesperidoside (5), one flavone C-glucoside; isoorientin (6), one phenolic acid; p-coumaric acid (7), one lignan; 4-ketopinoresinol (8) and two sterols; stigmasterol (9) and β-sitosterol-3-O-β-D-glucoside (10). The structural elucidations of isolated compounds were established on the basis of NMR and MS spectral analyses. All isolated compounds and biological activities for different extracts, n-hexane, ethyl acetate and n-butanol fractions (antiviral, antimicrobial and cytotoxic activities) of Dichanthium annulatum were done for the first time.
No takes yet. Share an insight, caveat, or question.
Awad et al. (2015) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: