528-53-0 Usage
Description
Delphinidin chloride is an anthocyanidin, a natural plant pigment that serves as the precursor to certain anthocyanins, which are responsible for the blue-red colors found in various flowers, fruits, and red wine. Delphinidin chloride is known for its antioxidant properties and its ability to induce the release of nitric oxide by vascular endothelium, leading to vasorelaxation. Delphinidin chloride also exhibits inhibitory effects on signaling through epithelial growth factor receptors, suppressing the expression of estrogen receptor α, and inducing apoptosis and autophagy at specific doses. Additionally, it inhibits the histone acetyltransferase activities of p300/CBP.
Uses
Used in Pharmaceutical Applications:
Delphinidin chloride is used as a pharmaceutical agent for its antioxidant properties and potential therapeutic effects on various health conditions. Its ability to induce vasorelaxation and inhibit signaling through epithelial growth factor receptors makes it a promising candidate for the treatment of cardiovascular diseases and certain types of cancer.
Used in Food Industry:
Delphinidin chloride is used as a natural colorant in the food industry, providing the blue-red hues to products such as grapes, cranberries, and pomegranates. Its presence in these fruits contributes to their vibrant colors and enhances their visual appeal to consumers.
Used in Cosmetics Industry:
Delphinidin chloride can be used in the cosmetics industry as an ingredient in skincare products due to its antioxidant properties. Its ability to protect the skin from oxidative stress and promote overall skin health makes it a valuable addition to various cosmetic formulations.
Used in Nutraceutical Applications:
Delphinidin chloride can be utilized in the development of nutraceutical products, which are designed to provide health benefits beyond basic nutrition. Its antioxidant and anti-inflammatory properties, as well as its potential to support cardiovascular and overall health, make it a suitable candidate for inclusion in dietary supplements and functional foods.
Check Digit Verification of cas no
The CAS Registry Mumber 528-53-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 528-53:
(5*5)+(4*2)+(3*8)+(2*5)+(1*3)=70
70 % 10 = 0
So 528-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O7.2ClH/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6;;/h1-5H,(H5-,16,17,18,19,20,21);2*1H/p-1
528-53-0Relevant articles and documents
Differences in the floral anthocyanin content of violet-blue flowers of Vinca minor L. and V. major L. (Apocynaceae)
Tatsuzawa, Fumi
, p. 365 - 369 (2015/08/24)
Two novel delphinidin 3-(tri or di)-glycoside-7-glycosides were isolated from the violet-blue flowers of Vinca minor L. and V. major L. (Family: Apocynaceae), and determined to be delphinidin 3-O-[2-O-(β-xylopyranosyl)-6-O-(α-rhamnopyranosyl)-β-galactopyranoside]-7-O-(α-rhamnopyranoside) [= delpphinidin 3-(2G-xylosylrobinobioside)-7-rhamnoside] as major floral anthocyanin of V. minor and delphinidin 3-O-[6-O-(α-rhamnopyranosyl)-β-galactopyranoside]-7-O-(α-rhamnopyranoside) [= delpphinidin 3-robinobioside-7-rhamnoside] as major floral anthocyanin of V. major by chemical and spectroscopic methods. In addition, chlorogenic acid and kaempferol 3-O-[6-O-(α-rhamnopyranosyl)-β-galactopyranoside]-7-O-(α-rhamnopyranoside) [= kaempferol 3-robinobioside-7-rhamnoside (robinin)] were identified in these flowers. In this paper, the relation between the structure of floral anthocyanins and classification of Vinca species was discussed.
Dimeric prodelphinidins from Limonium gmelinii roots. III
Zhusupova,Abil'kaeva
, p. 164 - 168 (2008/02/01)
Two dimeric proanthocyanidines identified as 2R,3R,4R-(-)-epigallocatechin- (4β→ 8)-2R,3R-(-)-epigallocatechin-3-O-gallate and 2R,3R,4R-(-)-epigallocatechin-(4β→8)-(-)-2R,3R,3,5,7,3′, 4′,6′-hexahydroxyflavan were isolated by adsorption chromatography over polyamide of the ethylacetate fraction of the aqueous alcohol extract of Limonium gmelinii roots. The former proanthocyanidine was isolated for the first time from sea lavender whereas the latter is new. 2006 Springer Science+Business Media, Inc.
Oligomeric proanthocyanidin glycosides of Clementsia semenovii and their biological activity. III
Kuliev,Kim,Vdovin,Abdullaev,Khushbaktova,Syrov
, p. 60 - 67 (2007/10/03)
The structures of two oligomeric proanthocyanidins isolated from roots of Clementsia semenovii have been established using chemical and spectral data. Animal studies showed that these compounds possess hypocholesterinemic, hypolipidemic, and anti-inflammatory activities.
