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41347-49-3

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41347-49-3 Usage

General Description

Anhydrotuberosin is a natural compound found in the tuber of the plant Anemarrhena asphodeloides. It belongs to the steroidal saponin group and has been found to have various biological activities, including anti-inflammatory, anti-cancer, and neuroprotective properties. Anhydrotuberosin has been studied for its potential use in the treatment of diseases such as cancer, diabetes, and neurodegenerative disorders due to its ability to modulate important cellular pathways and processes. Anhydrotuberosin has also shown potential as a therapeutic agent for conditions such as arthritis and inflammatory bowel disease. Its diverse pharmacological effects make it a promising candidate for further research and development of new treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 41347-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41347-49:
(7*4)+(6*1)+(5*3)+(4*4)+(3*7)+(2*4)+(1*9)=103
103 % 10 = 3
So 41347-49-3 is a valid CAS Registry Number.

41347-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 10,10-Dimethyl-6H,10H-chromeno[6',7':4,5]furo[3,2-c]chromen-3-ol

1.2 Other means of identification

Product number -
Other names Dehydrosimvastatin

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:41347-49-3 SDS

41347-49-3Relevant articles and documents

An enzyme-mimetic chemical conversion and biogenetic outline for chemical marker pterocarponoid oxygen heterocycles from Kudzu vine

Khan, Riaz A.

experimental part, p. 168 - 175 (2011/03/21)

An enzymatic chemical conversion of isoflavone and chemical marker oxygen-heterocycles pterocarponoids are carried out in an analogy to major subcellular enzymatic conversions involved in the natural biogenetic pathway and microbial interaction steps for oxygen-proliferated products obtained from bioactive fractions of widely occurring Kudzu plant, Pueraria tuberosa. An outline for biogenesis of major pterocarponoid constituents from principal biogenetic precursor, deoxytuberosin, is also proposed for P tuberosa.

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