X-ray crystallographic and validated HPTLC analysis of the biomarker chromone glucoside (schumanniofioside A) isolated from Acalypha fruticosa growing in Saudi Arabia

A chromone glucoside 2-methyl-5,7-dihydroxychromone 5-O-β-D-glucopyranoside (schumanniofioside A, compound 1) was isolated from the methanol extract of Acalypha fruticosa. The structure of compound 1 was fully assigned based on nuclear magnetic resonance (NMR) (1H, 13C and 2D) spectra and electrospr...

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Main Authors: Areej M. Al-Taweel (Author), Ghada A. Fawzy (Author), Shagufta Perveen (Author), Perwez Alam (Author), Ali A. El Gamal (Author)
Format: Book
Published: Elsevier, 2017-11-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Areej M. Al-Taweel  |e author 
700 1 0 |a Ghada A. Fawzy  |e author 
700 1 0 |a Shagufta Perveen  |e author 
700 1 0 |a Perwez Alam  |e author 
700 1 0 |a Ali A. El Gamal  |e author 
245 0 0 |a X-ray crystallographic and validated HPTLC analysis of the biomarker chromone glucoside (schumanniofioside A) isolated from Acalypha fruticosa growing in Saudi Arabia 
260 |b Elsevier,   |c 2017-11-01T00:00:00Z. 
500 |a 1319-0164 
500 |a 10.1016/j.jsps.2017.02.011 
520 |a A chromone glucoside 2-methyl-5,7-dihydroxychromone 5-O-β-D-glucopyranoside (schumanniofioside A, compound 1) was isolated from the methanol extract of Acalypha fruticosa. The structure of compound 1 was fully assigned based on nuclear magnetic resonance (NMR) (1H, 13C and 2D) spectra and electrospray ionization mass spectrum (ESI-MS) in addition to X-ray Crystallography. The molecules were packed in the crystal structure by eight intermolecular OH⋯O and CH⋯O interactions. The structure of compound 1 belongs to monoclinic, P21, a = 9.1989 (4) Å, b = 4.6651 (2) Å, c = 20.4042 (7) Å, β = 97.862 (3)°, V = 867.31 (6) Å3, Z = 2, wRref (F2) = 0.101, T = 100 K. Thus, the bond angles, bond lengths and absolute structure of compound 1 were confirmed by its X-ray structure. A validated HPTLC method was developed for the quantitative analysis of compound 1 in chloroform and methanol extracts of A. fruticosa. It was found to furnish a compact and sharp band of compound 1 at Rf = 0.13 ± 0.005 using chloroform, methanol and glacial acetic acid [17:3:0.5 (v/v/v)] as mobile phase. The LOD and LOQ for compound 1 were found to be 17.86 and 54.13 ng/band, respectively. Compound 1 was found in both chloroform and methanol extracts of the plant (0.03% w/w and 0.31% w/w, respectively). The proposed HPTLC method can be used for the further analysis of schumanniofioside A in different plant extracts, herbal formulations and biological samples as well as in process quality control. 
546 |a EN 
690 |a Acalypha fruticosa 
690 |a Schumanniofioside A 
690 |a Single-crystal X-ray 
690 |a HPTLC 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Saudi Pharmaceutical Journal, Vol 25, Iss 7, Pp 955-960 (2017) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1319016417300324 
787 0 |n https://doaj.org/toc/1319-0164 
856 4 1 |u https://doaj.org/article/bf9cc9d4c8be4b6aab8b0a02910377d7  |z Connect to this object online.