U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C15H11O7.Cl
Molecular Weight 338.697
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DELPHINIDIN CHLORIDE

SMILES

[Cl-].OC1=CC(O)=C2C=C(O)C(=[O+]C2=C1)C3=CC(O)=C(O)C(O)=C3

InChI

InChIKey=FFNDMZIBVDSQFI-UHFFFAOYSA-N
InChI=1S/C15H10O7.ClH/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);1H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Anthocyanins induce cell cycle perturbations and apoptosis in different human cell lines.
2004 Aug
Induction of apoptosis by the Anthocyanidins through regulation of Bcl-2 gene and activation of c-Jun N-terminal kinase cascade in hepatoma cells.
2005 Mar 9
Anthocyanins protect against A2E photooxidation and membrane permeabilization in retinal pigment epithelial cells.
2005 May-Jun
Delphinidin and cyanidin inhibit PDGF(AB)-induced VEGF release in vascular smooth muscle cells by preventing activation of p38 MAPK and JNK.
2006 Oct
Dietary flavones and flavonoles are inhibitors of poly(ADP-ribose)polymerase-1 in pulmonary epithelial cells.
2007 Oct
PGK1 induction by a hydrogen peroxide treatment is suppressed by antioxidants in human colon carcinoma cells.
2008 Jul
Delphinidin attenuates stress injury induced by oxidized low-density lipoprotein in human umbilical vein endothelial cells.
2010 Jan 5
Antifibrotic activity of anthocyanidin delphinidin in carbon tetrachloride-induced hepatotoxicity in mice.
2010 Jun 4
Pelargonidin activates the AhR and induces CYP1A1 in primary human hepatocytes and human cancer cell lines HepG2 and LS174T.
2013 Apr 26
Patents
Name Type Language
DELPHINIDIN CHLORIDE
Common Name English
DELPHINIDIN [MI]
Common Name English
3,5,7-TRIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-1-BENZOPYRYLIUM CHLORIDE (1:1)
Systematic Name English
DELPHINIDIN
MI  
Common Name English
DELPHINIDOL
Common Name English
3,3',4',5,5',7-HEXAHYDROXYFLAVYLIUM CHLORIDE
Systematic Name English
3,3',4',5,5',7-HEXAHYDROXY-2-PHENYLBENZOPYRYLIUM CHLORIDE
Common Name English
Classification Tree Code System Code
DSLD 3468 (Number of products:57)
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
NCI_THESAURUS C68444
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
Code System Code Type Description
CHEBI
38701
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
CAS
528-53-0
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
CHEBI
144775
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
WIKIPEDIA
DELPHINIDIN
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
MERCK INDEX
m4155
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID701019982
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
FDA UNII
EM6MD4AEHE
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-437-0
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
NCI_THESAURUS
C68446
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY
PUBCHEM
68245
Created by admin on Fri Dec 15 19:47:40 GMT 2023 , Edited by admin on Fri Dec 15 19:47:40 GMT 2023
PRIMARY