DELPHINIDIN CHLORIDE

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 Search

SMILES

[Cl-].OC1=CC2=[O+]C(C3=CC(O)=C(O)C(O)=C3)=C(O)C=C2C(O)=C1

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

Molecular Formula	C15H10O7
Molecular Weight	302.2357
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Targets

Primary Target	Pharmacology	Potency
regulation of membrane permeability 2 Target ID: GO:0090559 Sources: https://adisinsight.springer.com/drugs/800003473	Inhibitor 8504
Vascular endothelial growth factor receptor 2 112 Target ID: CHEMBL279 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27484508	Inhibitor 8504	5.09 nM [IC50]
Epidermal growth factor receptor erbB1 62 Target ID: CHEMBL203 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27484508	Inhibitor 8504	6.27 nM [IC50]

PubMed

Title	Date	PubMed
Pelargonidin activates the AhR and induces CYP1A1 in primary human hepatocytes and human cancer cell lines HepG2 and LS174T.	2013-04-26	23419638
Antifibrotic activity of anthocyanidin delphinidin in carbon tetrachloride-induced hepatotoxicity in mice.	2010-06-04	20371262
Delphinidin attenuates stress injury induced by oxidized low-density lipoprotein in human umbilical vein endothelial cells.	2010-01-05	19818742
Fyn kinase is a direct molecular target of delphinidin for the inhibition of cyclooxygenase-2 expression induced by tumor necrosis factor-alpha.	2009-04-01	19174152
Delphinidin modulates the DNA-damaging properties of topoisomerase II poisons.	2009-03-16	19182879
PGK1 induction by a hydrogen peroxide treatment is suppressed by antioxidants in human colon carcinoma cells.	2008-07	18603805
Dietary flavones and flavonoles are inhibitors of poly(ADP-ribose)polymerase-1 in pulmonary epithelial cells.	2007-10	17884996
Delphinidin and cyanidin inhibit PDGF(AB)-induced VEGF release in vascular smooth muscle cells by preventing activation of p38 MAPK and JNK.	2006-10	16921400
Induction of apoptosis by the Anthocyanidins through regulation of Bcl-2 gene and activation of c-Jun N-terminal kinase cascade in hepatoma cells.	2005-03-09	15740068
Anthocyanins protect against A2E photooxidation and membrane permeabilization in retinal pigment epithelial cells.	2005-03-05	15745429
Anthocyanins induce cell cycle perturbations and apoptosis in different human cell lines.	2004-08	15016660
The metabolism of dietary polyphenols and the relevance to circulating levels of conjugated metabolites.	2002-11	12592675
Antioxidant activity of black currant anthocyanin aglycons and their glycosides measured by chemiluminescence in a neutral pH region and in human plasma.	2002-08-28	12188603
Orally administered delphinidin 3-rutinoside and cyanidin 3-rutinoside are directly absorbed in rats and humans and appear in the blood as the intact forms.	2001-03	11312894

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:57:10 GMT 2025` Edited by `admin` on `Mon Mar 31 19:57:10 GMT 2025`
Record UNII	EM6MD4AEHE
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

DELPHINIDIN

Preferred Name

English

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

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)