134-04-3 Usage
Description
PELARGONIDIN CHLORIDE is an anthocyanidin chloride with pelargonidin as its cationic counterpart. It is a naturally occurring compound found in various plant sources and is known for its antioxidant and anthocyanidin properties.
Uses
Used in Pharmaceutical Industry:
PELARGONIDIN CHLORIDE is used as a pharmaceutical compound for its potential antidiabetic properties. It has been tested for its ability to help manage and treat diabetes.
Used in Cancer Research:
PELARGONIDIN CHLORIDE is used as a research compound for investigating the inhibitory effects on colon and liver cancer cells. Its antioxidant properties make it a promising candidate for cancer research.
Used in Antioxidant Studies:
PELARGONIDIN CHLORIDE is used as an antioxidant and anthocyanidin in studies evaluating its scavenging abilities against hydroperoxide and hydrogen peroxide. This helps in understanding its potential role in preventing oxidative stress and related diseases.
Used in Redox Potential Research:
PELARGONIDIN CHLORIDE is used as a research compound to study the relationship between its structure, antioxidant capacity, and redox potentials. This aids in understanding its potential applications in various fields, including pharmaceuticals and nutraceuticals.
Used in Pharmacological Studies:
PELARGONIDIN CHLORIDE is used as a flavonoid inhibitor in pharmacological studies investigating the use of flavonoids as inhibitors of CD38. This helps in understanding the compound's potential role in immune system regulation and other related functions.
Biochem/physiol Actions
Antioxidant and anthocyanidin.
Check Digit Verification of cas no
The CAS Registry Mumber 134-04-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134-04:
(5*1)+(4*3)+(3*4)+(2*0)+(1*4)=33
33 % 10 = 3
So 134-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O5.ClH/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15;/h1-7H,(H3-,16,17,18,19);1H
134-04-3Relevant articles and documents
Proanthocyanidins and a phloroglucinol derivative from Rumex acetosa L.
Bicker,Petereit,Hensel
experimental part, p. 483 - 495 (2010/06/15)
From the ethyl acetate soluble fraction of an acetone-water extract of the aerial parts of Rumex acetosa L. (Polygonaceae), a variety of monomeric flavan-3-ols (catechin, epicatechin, epicatechin-3-O-gallate), A- and B-type procyanidins and propelargonidins (15 dimers, 7 trimers, 2 tetramers) were isolated with 5 so far unknown natural products. Dimers: procyanidin B1, B2, B3, B4, B5, B7, A2, epiafzelechin-(4β→8)-epicatechin, epiafzelechin-(4β→8)-epicatechin-3-O-gallate (new natural product), epiafzelechin-(4β→6)-epicatechin-3-O-gallate (new natural product), epiafzelechin-3-O-gallate-(4β→8)-epicatechin-3-O-gallate, B2-3′-O-gallate, B2-3,3′-di-O-gallate, B5-3′-O-gallate, and B5-3,3′-di-O-gallate. Trimers: procyanidin C1, epiafzelechin-(4β→8)-epicatechin-(4β→8)-epicatechin (new natural product), epicatechin-(4β→8)-epicatechin-(4β→8)-catechin, cinnamtannin B1, cinnamtannin B1-3-O-gallate (new natural product), tentatively epicatechin-(2β→7, 4β→8)-epiafzelechin-(4α→8)-epicatechin (new natural product), and epicatechin-3-O-gallate-(4β→8)-epicatechin-3-O-gallate-(4β→8)-epicatechin-3-O-gallate. Tetramers: procyanidin D1 and parameritannin A1. All compounds were elucidated by ESI-MS, CD spectra, 1D- and 2D-NMR experiments as free phenols or peracetylated derivatives and, in part, after partial acid-catalysed degradation with phloroglucinol. A more abundant proanthocyanidin polymer was also isolated, purified and its chemical composition studied by 13C NMR. In addition a so far unknown phloroglucinolglycoside (1-O-β-d-(2,4-dihydroxy-6-methoxyphenyl)-6-O-(4-hydroxy-3,5-dimethoxybenzoyl)-glucopyranoside) was isolated.
