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41347-45-9

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41347-45-9 Usage

Description

(6aS)-6a,13aα-Dihydro-10,10-dimethyl-6H,10H-furo[3,2-c:4,5-g']bis[1]benzopyran-3,6aα-diol, also known as diosmetin, is a flavonoid compound derived from various plants, including citrus fruits and Chinese herbs. It is recognized for its potential health benefits, which encompass anti-inflammatory, antioxidant, and anticancer properties. Diosmetin also exhibits potential in preventing cardiovascular diseases and enhancing heart health, along with neuroprotective effects that could contribute to improved cognitive function.

Uses

Used in Dietary Supplements:
Diosmetin is utilized as an ingredient in dietary supplements for its wide range of health-promoting properties. It is particularly valued for its anti-inflammatory and antioxidant effects, which can contribute to overall well-being and support a healthy immune system.
Used in Herbal Medicine:
In the field of herbal medicine, diosmetin is employed for its potential therapeutic applications. Its presence in traditional remedies is attributed to its ability to address various health concerns, including inflammation and oxidative stress.
Used in Anticancer Applications:
Diosmetin is investigated for its potential as an anticancer agent, with studies exploring its effects on different types of cancer. It may play a role in modulating cellular processes that contribute to tumor growth and progression.
Used in Cardiovascular Health:
Diosmetin is also being studied for its potential role in preventing cardiovascular diseases. Its antioxidant and anti-inflammatory properties may help improve heart health and reduce the risk of related conditions.
Used in Cognitive Function Enhancement:
Due to its neuroprotective effects, diosmetin is being explored for its potential to enhance cognitive function and support brain health, particularly in conditions associated with cognitive decline.
Used in Pharmaceutical Research:
As a compound with diverse biological activities, diosmetin is a subject of interest in pharmaceutical research. Its potential applications in developing new drugs for various health conditions are being actively investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 41347-45-9 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 41347-45:
(7*4)+(6*1)+(5*3)+(4*4)+(3*7)+(2*4)+(1*5)=99
99 % 10 = 9
So 41347-45-9 is a valid CAS Registry Number.

41347-45-9SDS

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 (+)-tuberosin

1.2 Other means of identification

Product number -
Other names isotuberosin

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:41347-45-9 SDS

41347-45-9Upstream product

41347-45-9Downstream Products

41347-45-9Relevant 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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