| Literature DB >> 25900047 |
Toshihiro Murata1, Erdenechimeg Selenge, Saki Oikawa, Keita Ageishi, Javzan Batkhuu, Kenroh Sasaki, Fumihiko Yoshizaki.
Abstract
A diterpenoid diglucoside (12,19-di-O-β-D-glucopyranosyl-11-hydroxyabieta-8,11,13-triene-19-one), isoscutellarein 7-O-[β-D-xylopyranosyl-(1→2)]-β-D-glucopyranoside, isoscutellarein 7-O-[α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside, hypolaetin 7-O-[6″-O-(p-E-coumaroyl)]-β-D-glucopyranoside, hypolaetin 7-O-[6″-O-(E-caffeoyl)]-β-D-glucopyranoside, and 15 known compounds were isolated from aerial parts of the Mongolian medicinal plant Caryopteris mongolica. The cholinesterase-inhibitory activities of the constituents were estimated. The abietane diterpenoids (12-O-demethylcryptojaponol and 6α-hydroxydemethylcryptojaponol) showed potent inhibitory activity against acetylcholinesterase from human erythrocytes and electric eel, and against butyrylcholinesterase from horse serum.Entities:
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Year: 2015 PMID: 25900047 DOI: 10.1007/s11418-015-0908-6
Source DB: PubMed Journal: J Nat Med ISSN: 1340-3443 Impact factor: 2.343