IMPPAT Phytochemical information: 
Delphinidin
Delphinidin
Summary

SMILES: Oc1cc(O)c2c(c1)[o+]c(c(c2)O)c1cc(O)c(c(c1)O)O.[Cl-]
InChI: 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
InChIKey: FFNDMZIBVDSQFI-UHFFFAOYSA-N
DeepSMILES: OcccO)ccc6)[o+]ccc6)O))cccO)ccc6)O))O.[Cl-]
Scaffold Graph/Node/Bond level: c1ccc(-c2ccc3ccccc3[o+]2)cc1
Scaffold Graph/Node level: C1CCC(C2CCC3CCCCC3O2)CC1
Scaffold Graph level: C1CCC(C2CCC3CCCCC3C2)CC1
Functional groups: [Cl-]; cO; c[o+]c
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Flavonoids
ClassyFire Subclass: Hydroxyflavonoids
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Flavonoids
NP Classifier Class: Anthocyanidins
Synonymous chemical names:
delphinidin, delphinidin chloride, delphinidine, delphinidol
External chemical identifiers:
CID:68245; ChEMBL:CHEMBL590878; ChEBI:38701; FDASRS:EM6MD4AEHE; SureChEMBL:SCHEMBL22369; MolPort-003-932-836
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Delphinidin
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 338.7
Log P RDKit -0.38
Topological polar surface area (Å2) RDKit 132.68
Number of hydrogen bond acceptors RDKit 6
Number of hydrogen bond donors RDKit 6
Number of carbon atoms RDKit 15
Number of heavy atoms RDKit 23
Number of heteroatoms RDKit 8
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 0
Stereochemical complexity RDKit 0
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 15
Number of sp3 hybridized carbon atoms RDKit 0
Shape complexity RDKit 0
Number of rotatable bonds RDKit 1
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 2
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 3
Total number of rings RDKit 3
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 3
Delphinidin
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 1
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 0
Ghose filter RDKit Passed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.263
Delphinidin
ADMET properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -7.5
Number of PAINS structural alerts SwissADME 1.0
Number of Brenk structural alerts SwissADME 2.0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes
Delphinidin
Predicted human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000270202AKT1814
ENSP00000311032CASP3700
ENSP00000337915CYP3A4800
ENSP00000346671FYN800
ENSP00000353483MAPK8726
ENSP00000354522TOP1700
ENSP00000355759PARP1700
ENSP00000356438PTGS2818
ENSP00000361125VEGFA818
ENSP00000369050CYP1A1730
ENSP00000396538NFAT5800
ENSP00000411532TOP2A700
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.