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521-65-3

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521-65-3 Usage

Definition

ChEBI: A member of the class of xanthones that is the 5-O-methyl derivative of bellidifolin. Isolated from Centaurium erythraea and Swertia chirayita, it exhibits hypoglycemic activity.

Check Digit Verification of cas no

The CAS Registry Mumber 521-65-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 521-65:
(5*5)+(4*2)+(3*1)+(2*6)+(1*5)=53
53 % 10 = 3
So 521-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O6/c1-19-7-5-9(17)12-11(6-7)21-15-10(20-2)4-3-8(16)13(15)14(12)18/h3-6,16-17H,1-2H3

521-65-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name swerchirin

1.2 Other means of identification

Product number -
Other names 3,5-Dimethoxy-1,8-dihydroxyxanthone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:521-65-3 SDS

521-65-3Relevant articles and documents

Xanthone glycoside constituents of Swertia kouitchensis with α-glucosidase inhibitory activity

Wan, Luo-Sheng,Min, Qiu-Xia,Wang, Yong-Long,Yue, Yao-Dong,Chen, Jia-Chun

, p. 1248 - 1253 (2013/08/23)

Ten new xanthone glycosides, kouitchensides A-J (1-10), and 11 known analogues were isolated from an n-butanol fraction of Swertia kouitchensis. The structures of these glycosides were determined on the basis of extensive spectroscopic data interpretation and comparison with data reported in the literature. In an in vitro test, compounds 2, 4, 5, 6, 11, 12, and 13 (IC 50 values in the range 126 to 451 μM) displayed more potent inhibitory effects against α-glucosidase activity than the positive control, acarbose (IC50 value of 627 μM).

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