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41347-49-3

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41347-49-3 Usage

Description

Anhydrotuberosin, a natural compound derived from the tuber of the plant Anemarrhena asphodeloides, belongs to the steroidal saponin group. It exhibits a range of biological activities, including anti-inflammatory, anti-cancer, and neuroprotective properties. Its ability to modulate crucial cellular pathways and processes has positioned Anhydrotuberosin as a promising candidate for the treatment of various diseases and conditions.

Uses

Used in Pharmaceutical Industry:
Anhydrotuberosin is used as a therapeutic agent for its anti-inflammatory properties, making it a potential treatment for conditions such as arthritis and inflammatory bowel disease. Its capacity to modulate cellular pathways involved in inflammation offers a promising avenue for managing these disorders.
Used in Oncology:
In the field of oncology, Anhydrotuberosin is utilized as an anti-cancer agent. Its potential to target and modulate various cellular processes associated with cancer growth and progression positions it as a candidate for the development of novel cancer therapies.
Used in Neurodegenerative Disorder Treatment:
Anhydrotuberosin is employed as a neuroprotective agent, offering potential benefits in the treatment of neurodegenerative disorders. Its ability to support neuronal health and function may contribute to the management and mitigation of symptoms associated with such conditions.
Used in Diabetes Management:
Anhydrotuberosin's potential role in diabetes management stems from its capacity to influence cellular processes relevant to glucose metabolism and insulin sensitivity. This makes it a candidate for further research into its utility in developing treatments for diabetes and related metabolic disorders.
Overall, the diverse pharmacological effects of Anhydrotuberosin underscore its potential across multiple medical fields, warranting continued research and development to harness its therapeutic capabilities fully.

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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