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119309-02-3

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119309-02-3 Usage

Description

Atalantoflavone is a natural chemical compound belonging to the biflavonoid class, predominantly found in plant species such as Ginkgo biloba and Hypericum perforatum. It has garnered attention for its potential therapeutic effects, which include anti-inflammatory, anti-cancer, and neuroprotective properties. Preclinical studies have demonstrated its ability to inhibit cancer cell growth, reduce inflammation, and protect against neurodegenerative diseases. Furthermore, atalantoflavone exhibits antioxidant and anti-microbial activities, making it a promising candidate for further research into its applications in medicine and healthcare. As a biologically active compound, atalantoflavone holds the potential to offer a range of health benefits, although additional research is necessary to fully understand its mechanisms and therapeutic applications.

Uses

Used in Pharmaceutical Industry:
Atalantoflavone is used as a therapeutic agent for its anti-inflammatory properties, helping to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Oncology:
Atalantoflavone is used as an anti-cancer agent, showing promise in inhibiting the growth of cancer cells and potentially offering a novel treatment option for various types of cancer.
Used in Neuroprotection:
Atalantoflavone is used as a neuroprotective agent, with its potential to protect against neurodegenerative diseases and support brain health.
Used in Antioxidant Formulations:
Atalantoflavone is used as an antioxidant, contributing to the prevention of cellular damage caused by free radicals and supporting overall health.
Used in Anti-microbial Applications:
Atalantoflavone is used as an anti-microbial agent, demonstrating activity against certain microorganisms and potentially serving as a component in treatments for microbial infections.

Check Digit Verification of cas no

The CAS Registry Mumber 119309-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,3,0 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119309-02:
(8*1)+(7*1)+(6*9)+(5*3)+(4*0)+(3*9)+(2*0)+(1*2)=113
113 % 10 = 3
So 119309-02-3 is a valid CAS Registry Number.

119309-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-Aminoethyl)-2-hydroxyphenyl benzoate

1.2 Other means of identification

Product number -
Other names atalantoflavone

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:119309-02-3 SDS

119309-02-3Relevant articles and documents

Cytotoxicity and Anti-inflammatory Properties of Apigenin-Derived Isolaxifolin

Chen, Yongsheng,Chen, Wan-Na,Hu, Nan,Banwell, Martin G.,Ma, Chenxi,Gardiner, Michael G.,Lan, Ping

, p. 2451 - 2459 (2019/09/30)

The rare flavonoid isolaxifolin, a potent insecticide, has been touted as a potential grain-protecting agent. In order to assess any impact of this natural product on human health and to explore its various other biological properties, we have established a semisynthesis from the simpler but structurally related and more abundant natural product apigenin. The five-step reaction sequence has provided, for the first time, sufficient material for an in-depth evaluation of the cytotoxic properties of the title natural product. The impact of isolaxifolin on certain pro-inflammatory cytokines in murine macrophage RAW 264.7 cells has also been examined. Such studies have revealed that isolaxifolin displays no toxic effects toward normal cells while displaying greater cytotoxicities against certain cancer cell lines than its synthetic precursor apigenin. Furthermore, unlike apigenin, isolaxifolin only reduced NO, TNF-α, and IL-6 secretions in LPS-induced RAW 264.7 cells in a rather modest and dose-independent manner.

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