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19312-13-1

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19312-13-1 Usage

Description

(2E)-1-(2,5-dihydroxyphenyl)-3-phenylprop-2-en-1-one, commonly known as chalcone, is a natural product belonging to the chalcone class of organic compounds. It is found in plants and serves as a precursor for the synthesis of flavonoids. Chalcone has been studied for its potential biological activities, such as antioxidant, anti-inflammatory, and anticancer properties. It is also considered an important building block for the development of new drugs and has been investigated for its potential use in therapeutic agents for various diseases.

Uses

Used in Pharmaceutical Industry:
Chalcone is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs. Its unique structure and biological activities make it a valuable building block for medicinal chemistry.
Used in Antioxidant Applications:
Chalcone is utilized as an antioxidant, protecting cells from oxidative stress and damage caused by reactive oxygen species. Its antioxidant properties can be beneficial in the prevention and treatment of various diseases associated with oxidative stress.
Used in Anti-inflammatory Applications:
Chalcone is employed as an anti-inflammatory agent, helping to reduce inflammation and alleviate symptoms associated with inflammatory conditions. Its anti-inflammatory properties can be useful in the management of various diseases characterized by chronic inflammation.
Used in Anticancer Applications:
Chalcone is used as an anticancer agent, exhibiting potential inhibitory effects on the growth and progression of cancer cells. Its anticancer properties make it a promising candidate for the development of therapeutic agents against various types of cancer.
Used in Drug Development:
Chalcone is used in the development of therapeutic agents for various diseases, leveraging its biological activities and potential synergistic effects with other compounds. Its diverse applications in medicine make it a valuable asset in the search for novel treatments and cures.

Check Digit Verification of cas no

The CAS Registry Mumber 19312-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,1 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19312-13:
(7*1)+(6*9)+(5*3)+(4*1)+(3*2)+(2*1)+(1*3)=91
91 % 10 = 1
So 19312-13-1 is a valid CAS Registry Number.

19312-13-1SDS

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 1-(2,5-dihydroxyphenyl)-3-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2',5'-dihydroxychalcone

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:19312-13-1 SDS

19312-13-1Relevant articles and documents

Flavanone-based fluorophores with aggregation-induced emission enhancement characteristics for mitochondria-imaging and zebrafish-imaging

He, Feng,Li, Na,Liu, Liyan,Luo, Huiqing,Wang, Huaqiao,Yang, Depo

, (2020)

Fluorophores with aggregation-induced emission enhancement (AIEE) characteristics applied in bioimaging have attracted more and more attention in recent years. In this work, a series of flavanone compounds with AIEE characteristics was developed and applied to fluorescence imaging of mitochondria and zebrafish. The compounds were readily prepared by the thermal dehydration of chalcone that was obtained by the reaction of o-hydroxyacetophenone and benzaldehyde. Two of these compounds showed significant AIEE characteristics by fluorescence performance experiments, including optical spectra, fluorescence spectra, fluorescence quantum yield (?F), fluorescence lifetime, and scanning electron microscopy (SEM). Compared with traditional organic fluorescent dyes, these compounds have high fluorescence emission and high fluorescence quantum yield in solid or aggregated state, which overcomes the shortcoming of aggregation-caused quenching (ACQ). More importantly, the two compounds exhibited low cytotoxicity and good cytocompatibility in A549 lung cells at the experimental concentration range and they specifically targeted mitochondria, which make it of great potential use in mitochondria labeling. In addition, they were embryonic membrane permeable and had different affinities for different tissues and organs of zebrafish, but mainly distributed in the digestive system, providing a basis for the application of such compounds in bioimaging. These AIEE compounds with superior properties could be of great potential use in mitochondria imaging and other in vivo studies.

Pharmacophore model of the quercetin binding site of the SIRT6 protein

Ravichandran,Singh,Donnelly,Migliore,Johnson,Fishwick,Luke,Martin,Maudsley,Fugmann,Moaddel

, p. 38 - 46 (2014/03/21)

SIRT6 is a histone deacetylase that has been proposed as a potential therapeutic target for metabolic disorders and the prevention of age-associated diseases. We have previously reported on the identification of quercetin and vitexin as SIRT6 inhibitors,

Synthesis of novel flavone acyl esters and correlation of log P value with antioxidant and antimicrobial activity

Jayashree,Thejaswini,Nayak, Yogendra,Kumar, D. Vijay

experimental part, p. 1055 - 1066 (2012/03/26)

Three series of flavones namely 6-hydroxy flavone, 6-chloro-3-hydroxy flavone, 3,6-dihydroxy flavone were synthesized. They were further benzoylated with different aromatic acid chlorides in the presence of pyridine gave three of acyl esters series (SCF 1 to 8, SHF 1 to 8 and SDF 1 to 8). The yields of all the substituted flavones were found satisfactory. These compounds were purified, characterized by their spectral data. log P and pKa value. They were screened for in vitro radical (DPP?) scavenging activity, showed appreciable activity. 7 compounds showed antimicrobial activity against Gram-positive bacteria. Further, the MIC values of these 7 compounds were also determined. All the compounds showing antioxidant activity also showed antibacterial activity. The relationship between log P, antioxidant and antibacterial activity was established.

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