86831-54-1

86831-54-1 structure

Name: Rhodiosin
Chemical Name: herbacetin 7-O-(3''-O-β-D-glucopyranosyl-α-L-rhamnopyranoside)
CAS Number: 86831-54-1
Molecular Formula: C₂₇H₃₀O₁₆
Molecular Weight: 610.518
Catalog: Signaling Pathways Neuronal Signaling AChE
Create Date: 2018-06-27 17:20:45
Modify Date: 2024-01-04 20:37:46
Rhodiosin, isolated from the root of Rhodiola crenulata, is a specific non-competitive cytochrome P450 2D6 inhibitor with an IC50 of 0.420 μM and a Ki of 0.535 μM[1]. Rhodiosin exhibits potent, dose-dependent inhibitory effects on acetylcholinesterase (AChE) with IC50 ranged from 57.50 to 2.43 μg/mL[2]. Rhodiosin exhibits potent DPPH free radical scavenging activities, with an IC50 of 27.77 μM[3].

Name	herbacetin 7-O-(3''-O-β-D-glucopyranosyl-α-L-rhamnopyranoside)
Synonyms	herbacetin 7-O-(3'-O-β-D-glucopyranosyl-α-L-rhamnopyranoside) 3,5,8-Trihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-deoxy-3-O-β-D-glucopyranosyl-α-L-mannopyranoside Herbacetin-7-O-glucorhamnoside 4H-1-BENZOPYRAN-4-ONE,7-[(6-DEOXY-3-O-B-D-GLUCOPYRANOSYL-A-L-MANNOPYRANOSYL)OXY]-3,5,8-TRIHYDROXY-2-(4-HYDROXYPHENYL)- 4H-1-Benzopyran-4-one, 7-[(6-deoxy-3-O-β-D-glucopyranosyl-α-L-mannopyranosyl)oxy]-3,5,8-trihydroxy-2-(4-hydroxyphenyl)- Rhodiosin

Description	Rhodiosin, isolated from the root of Rhodiola crenulata, is a specific non-competitive cytochrome P450 2D6 inhibitor with an IC50 of 0.420 μM and a Ki of 0.535 μM[1]. Rhodiosin exhibits potent, dose-dependent inhibitory effects on acetylcholinesterase (AChE) with IC50 ranged from 57.50 to 2.43 μg/mL[2]. Rhodiosin exhibits potent DPPH free radical scavenging activities, with an IC50 of 27.77 μM[3].
Related Catalog	Research Areas >> Metabolic Disease Signaling Pathways >> Neuronal Signaling >> AChE
Target	IC50: 0.420 μM (cytochrome P450 2D6)[1]；57.50-2.43 μg/mL (AChE)[2]；27.77 μM (DPPH free radical scavenging)[3]
References	[1]. Xu W, et al. Two potent cytochrome P450 2D6 inhibitors found in Rhodiola rosea. Pharmazie. 2013 Dec;68(12):974-6. [2]. Li FJ, et al. Molecular interaction studies of acetylcholinesterase with potential acetylcholinesterase inhibitors from the root of Rhodiola crenulata using molecular docking and isothermal titration calorimetry methods. Int J Biol Macromol. 2017 Nov;104(Pt A):527-532. [3]. Choe KI, et al. The antioxidant and anti-inflammatory effects of phenolic compounds isolated from the root of Rhodiola sachalinensis A. BOR. Molecules. 2012 Sep 27;17(10):11484-94.