IMPPAT Phytochemical information: 
Anthocyanin 1

Anthocyanin 1
Summary

SMILES: OC[C@H]1O[C@@H](Oc2cc(O)cc3c2cc(O[C@@H]2O[C@H](COC(=O)/C=C/c4ccc(cc4)O[C@@H]4O[C@H](COC(=O)C=Cc5ccc(c(c5)O[C@H]5O[C@@H](CO)[C@@H]([C@H]([C@@H]5O)O)O)O)[C@H]([C@@H]([C@H]4O)O)O)[C@H]([C@@H]([C@H]2O[C@H]2O[C@@H](COC(=O)C=Cc4ccc(c(c4)O[C@@H]4O[C@H](CO)[C@H]([C@@H]([C@H]4O)O)O)O)[C@@H]([C@H]([C@@H]2O)O)O)O)O)c([o+]3)c2ccc(c(c2)O)O)[C@@H]([C@H]([C@@H]1O)O)O
InChI: InChI=1S/C78H88O44/c79-23-45-54(90)60(96)67(103)74(116-45)112-41-21-33(82)20-40-35(41)22-44(71(111-40)32-8-13-36(83)39(86)19-32)115-78-72(122-77-70(106)64(100)58(94)49(120-77)27-108-53(89)16-7-31-4-12-38(85)43(18-31)114-76-69(105)62(98)56(92)47(25-81)118-76)65(101)59(95)50(121-78)28-109-51(87)14-5-29-1-9-34(10-2-29)110-73-66(102)63(99)57(93)48(119-73)26-107-52(88)15-6-30-3-11-37(84)42(17-30)113-75-68(104)61(97)55(91)46(24-80)117-75/h1-22,45-50,54-70,72-81,90-106H,23-28H2,(H4-,82,83,84,85,86,88,89)/p+1/b14-5+/t45-,46+,47-,48-,49+,50-,54-,55+,56-,57-,58+,59-,60+,61-,62+,63+,64-,65+,66-,67-,68+,69-,70+,72-,73-,74-,75+,76-,77-,78-/m1/s1
InChIKey: RGVQQOWPZHERDC-WVYMXQQSSA-O
DeepSMILES: OC[C@H]O[C@@H]OcccO)ccc6ccO[C@@H]O[C@H]COC=O)/C=C/cccccc6))O[C@@H]O[C@H]COC=O)C=Ccccccc6)O[C@H]O[C@@H]CO))[C@@H][C@H][C@@H]6O))O))O)))))))O))))))))))[C@H][C@@H][C@H]6O))O))O)))))))))))))))[C@H][C@@H][C@H]6O[C@H]O[C@@H]COC=O)C=Ccccccc6)O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O)))))))O))))))))))[C@@H][C@H][C@@H]6O))O))O)))))))O))O))))))c[o+]6)cccccc6)O))O)))))))))))))))[C@@H][C@H][C@@H]6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=Cc1cccc(OC2CCCCO2)c1)OCC1CCCC(Oc2ccc(C=CC(=O)OCC3CCC(OC4CCCC(COC(=O)C=Cc5cccc(OC6CCCCO6)c5)O4)C(Oc4cc5c(OC6CCCCO6)cccc5[o+]c4-c4ccccc4)O3)cc2)O1
Scaffold Graph/Node level: OC(CCC1CCCC(OC2CCCCO2)C1)OCC1CCCC(OC2CCC(CCC(O)OCC3CCC(OC4CCCC(COC(O)CCC5CCCC(OC6CCCCO6)C5)O4)C(OC4CC5C(OC6CCCCO6)CCCC5OC4C4CCCCC4)O3)CC2)O1
Scaffold Graph level: CC(CCC1CCCC(CC2CCCCC2)C1)CCC1CCCC(CC2CCC(CCC(C)CCC3CCC(CC4CCCC(CCC(C)CCC5CCCC(CC6CCCCC6)C5)C4)C(CC4CC5C(CC6CCCCC6)CCCC5CC4C4CCCCC4)C3)CC2)C1
Functional groups: CO; CO[C@@H](C)OC; c/C=C/C(=O)OC; cC=CC(=O)OC; cO; cO[C@@H](C)OC; cO[C@H](C)OC; c[o+]c
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Flavonoids
ClassyFire Subclass: Flavonoid glycosides
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Flavonoids
NP Classifier Class: Anthocyanidins
Synonymous chemical names:
anthocyanin 1
External chemical identifiers:
CID:101115386
Chemical structure download


Anthocyanin 1
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 1730.53
Log P RDKit -6.58
Topological polar surface area (Å2) RDKit 706.71
Number of hydrogen bond acceptors RDKit 43
Number of hydrogen bond donors RDKit 25
Number of carbon atoms RDKit 78
Number of heavy atoms RDKit 122
Number of heteroatoms RDKit 44
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 30
Stereochemical complexity RDKit 0.38
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 42
Number of sp3 hybridized carbon atoms RDKit 36
Shape complexity RDKit 0.46
Number of rotatable bonds RDKit 31
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 6
Number of aliphatic rings RDKit 6
Number of aromatic carbocycles RDKit 5
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 6
Total number of rings RDKit 12
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 6
Number of saturated rings RDKit 6
Number of Smallest Set of Smallest Rings (SSSR) RDKit 12


Anthocyanin 1
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 3
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 4
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.0071