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114175-98-3

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114175-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114175-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,7 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114175-98:
(8*1)+(7*1)+(6*4)+(5*1)+(4*7)+(3*5)+(2*9)+(1*8)=113
113 % 10 = 3
So 114175-98-3 is a valid CAS Registry Number.

114175-98-3SDS

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 cecropiacic acid

1.2 Other means of identification

Product number -
Other names (1R,4aR,4bS,6aS,9R,10R,10aS)-1-Carboxymethyl-2-(1-carboxy-1-methyl-ethyl)-10-hydroxy-1,4a,4b,9,10-pentamethyl-1,3,4,4a,4b,5,6,7,8,9,10,10a,12,12a-tetradecahydro-2H-chrysene-6a-carboxylic acid

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:114175-98-3 SDS

114175-98-3Upstream product

114175-98-3Downstream Products

114175-98-3Relevant articles and documents

Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina

Morikawa, Toshio,Ninomiya, Kiyofumi,Imura, Katsuya,Yamaguchi, Takahiro,Akagi, Yoshinori,Yoshikawa, Masayuki,Hayakawa, Takao,Muraoka, Osamu

, p. 169 - 181 (2014)

A methanol extract from the tuberous roots of Potentilla anserina (Rosaceae) exhibited hepatoprotective effects against d-galactosamine (d-GalN)/lipopolysaccharide-induced liver injuries in mice. Six triterpene 28-O-monoglucopyranosyl esters, potentillanosides A-F, were isolated from the extract along with 32 known compounds, including 15 triterpenes. The structures of potentillanosides A-F were determined on the basis of spectroscopic properties and chemical evidence. Four ursane-type triterpene 28-O-monoglycosyl esters, potentillanoside A (IC50 = 46.7 μM), 28-O-β-d- glucopyranosyl pomolic acid (IC50 = 9.5 μM), rosamutin (IC 50 = 35.5 μM), and kaji-ichigoside F1 (IC50 = 14.1 μM), inhibited d-GalN-induced cytotoxicity in primary cultured mouse hepatocytes. Among these four triterpenes, potentillanoside A, rosamutin, and kaji-ichigoside F1 exhibited in vivo hepatoprotective effects at doses of 50-100 mg/kg, p.o. The mode of action was ascribable to the reduction in cytotoxicity caused by d-GalN.

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