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Graveobioside A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63808-23-1

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63808-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63808-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,0 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63808-23:
(7*6)+(6*3)+(5*8)+(4*0)+(3*8)+(2*2)+(1*3)=131
131 % 10 = 1
So 63808-23-1 is a valid CAS Registry Number.

63808-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name luteolin 7-O-β-D-apiofuranosyl-(1->2)-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names graveobioside A

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:63808-23-1 SDS

63808-23-1Upstream product

63808-23-1Relevant articles and documents

Absorption and Metabolism of Luteolin in Rats and Humans in Relation to in Vitro Anti-inflammatory Effects

Hayasaka, Natsumi,Shimizu, Naoki,Komoda, Toshikazu,Mohri, Satoshi,Tsushida, Tojiro,Eitsuka, Takahiro,Miyazawa, Teruo,Nakagawa, Kiyotaka

, p. 11320 - 11329 (2018/11/20)

Luteolin is a flavonoid present in plants in the form of aglycone or glucosides. In this study, luteolin glucosides (i.e., luteolin-7-O-β-d-glucoside, luteolin-7-O-[2-(β-d-apiosyl)-β-d-glucoside], and luteolin-7-O-[2-(β-d-apiosyl)-6-malonyl-β-d-glucoside]) prepared from green pepper leaves as well as luteolin aglycone were orally administered to rats. Regardless of the administered luteolin form, luteolin glucuronides were mainly detected from plasma and organs. Subsequently, luteolin aglycone, the most absorbed form of luteolin in rats, was orally administered to humans. As a result, luteolin-3′-O-sulfate was mainly identified from plasma, suggesting that not only luteolin form but also animal species affect the absorption and metabolism of luteolin. When LPS-treated RAW264.7 cells were treated with luteolin glucuronides and luteolin sulfate (the characteristic metabolites identified from rats and humans, respectively), the different luteolin conjugates were metabolized in different ways, suggesting that such difference in metabolism results in their difference in anti-inflammatory effects.

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