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=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

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

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

Approval Year

Targets

Primary Target	Pharmacology	Potency
regulation of membrane permeability 2 Target ID: GO:0090559 Sources: https://adisinsight.springer.com/drugs/800003473	Inhibitor 8297
Vascular endothelial growth factor receptor 2 104 Target ID: CHEMBL279 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27484508	Inhibitor 8297	5.09 nM [IC50]
Epidermal growth factor receptor erbB1 58 Target ID: CHEMBL203 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27484508	Inhibitor 8297	6.27 nM [IC50]

PubMed

Title	Date	PubMed
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 Mar	11312894
Antioxidant activity of black currant anthocyanin aglycons and their glycosides measured by chemiluminescence in a neutral pH region and in human plasma.	2002 Aug 28	12188603
The metabolism of dietary polyphenols and the relevance to circulating levels of conjugated metabolites.	2002 Nov	12592675
Anthocyanins induce cell cycle perturbations and apoptosis in different human cell lines.	2004 Aug	15016660
Antifibrotic activity of anthocyanidin delphinidin in carbon tetrachloride-induced hepatotoxicity in mice.	2010 Jun 4	20371262
Pelargonidin activates the AhR and induces CYP1A1 in primary human hepatocytes and human cancer cell lines HepG2 and LS174T.	2013 Apr 26	23419638

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:47:40 GMT 2023` Edited by `admin` on `Fri Dec 15 19:47:40 GMT 2023`
Record UNII	EM6MD4AEHE
Record Status	`Validated (UNII)`
Record Version

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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

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)