IMPPAT Phytochemical information: 
Ternatin A2

Ternatin A2
Summary

SMILES: OC[C@@H]1O[C@H](Oc2ccc(cc2)/C=CC(=O)OC[C@@H]2O[C@H](Oc3ccc(cc3)/C=CC(=O)OC[C@H]3O[C@H](Oc4cc(cc(c4O)O[C@H]4O[C@@H](COC(=O)/C=Cc5ccc(cc5)O[C@H]5O[C@@H](CO)[C@@H]([C@@H]([C@H]5O)O)O)[C@@H]([C@@H]([C@H]4O)O)O)c4[o+]c5cc(O)cc(c5cc4O[C@H]4O[C@@H](COC(=O)CC(=O)O)[C@@H]([C@@H]([C@H]4O)O)O)O)[C@@H]([C@@H]([C@@H]3O)O)O)[C@@H]([C@H]([C@H]2O)O)O)[C@@H]([C@H]([C@H]1O)O)O
InChI: InChI=1S/C81H90O46/c82-25-45-57(93)63(99)69(105)76(122-45)115-36-10-1-31(2-11-36)7-16-52(88)111-27-47-59(95)65(101)71(107)78(124-47)117-38-14-5-33(6-15-38)9-18-54(90)113-29-49-61(97)67(103)73(109)80(126-49)120-43-20-34(75-44(23-39-40(85)21-35(84)22-41(39)118-75)121-81-74(110)68(104)62(98)50(127-81)30-114-55(91)24-51(86)87)19-42(56(43)92)119-79-72(108)66(102)60(96)48(125-79)28-112-53(89)17-8-32-3-12-37(13-4-32)116-77-70(106)64(100)58(94)46(26-83)123-77/h1-23,45-50,57-74,76-83,93-110H,24-30H2,(H3-,84,85,86,87,92)/p+1/b16-7-,17-8-,18-9-/t45-,46-,47-,48-,49+,50-,57-,58-,59-,60-,61+,62-,63-,64-,65-,66-,67+,68-,69+,70+,71+,72+,73+,74+,76-,77-,78-,79-,80-,81-/m0/s1
InChIKey: SIVINWHAEBFOIY-XLRMAADOSA-O
DeepSMILES: OC[C@@H]O[C@H]Occcccc6))/C=CC=O)OC[C@@H]O[C@H]Occcccc6))/C=CC=O)OC[C@H]O[C@H]Occcccc6O))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)))))))))))))))[C@@H][C@@H][C@H]6O))O))O))))))))c[o+]cccO)ccc6cc%10O[C@H]O[C@@H]COC=O)CC=O)O))))))[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))O))O)))))))))))))))[C@@H][C@H][C@H]6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=Cc1ccc(OC2CCCCO2)cc1)OCC1CCCC(Oc2ccc(C=CC(=O)OCC3CCCC(Oc4cc(OC5CCCC(COC(=O)C=Cc6ccc(OC7CCCCO7)cc6)O5)cc(-c5[o+]c6ccccc6cc5OC5CCCCO5)c4)O3)cc2)O1
Scaffold Graph/Node level: OC(CCC1CCC(OC2CCCCO2)CC1)OCC1CCCC(OC2CCC(CCC(O)OCC3CCCC(OC4CC(OC5CCCC(COC(O)CCC6CCC(OC7CCCCO7)CC6)O5)CC(C5OC6CCCCC6CC5OC5CCCCO5)C4)O3)CC2)O1
Scaffold Graph level: CC(CCC1CCC(CC2CCCCC2)CC1)CCC1CCCC(CC2CCC(CCC(C)CCC3CCCC(CC4CC(CC5CCCC(CCC(C)CCC6CCC(CC7CCCCC7)CC6)C5)CC(C5CC6CCCCC6CC5CC5CCCCC5)C4)C3)CC2)C1
Functional groups: CC(=O)O; CO; COC(C)=O; c/C=CC(=O)OC; cO; 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:
ternatin a2
External chemical identifiers:
CID:101063539
Chemical structure download


Ternatin A2
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 1800.57
Log P RDKit -6.61
Topological polar surface area (Å2) RDKit 729.85
Number of hydrogen bond acceptors RDKit 44
Number of hydrogen bond donors RDKit 24
Number of carbon atoms RDKit 81
Number of heavy atoms RDKit 127
Number of heteroatoms RDKit 46
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 30
Stereochemical complexity RDKit 0.37
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 44
Number of sp3 hybridized carbon atoms RDKit 37
Shape complexity RDKit 0.46
Number of rotatable bonds RDKit 35
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


Ternatin A2
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 0.0063