Summary
SMILES: COc1c(C)c(O)c(c(c1C(=O)C(C)C)O)Cc1c(O)cc(c2c1O[C@@H]([C@H](C2)O)c1ccc(c(c1)O)O)OInChI: InChI=1S/C28H30O10/c1-11(2)23(34)22-25(36)16(24(35)12(3)26(22)37-4)8-14-18(30)10-19(31)15-9-21(33)27(38-28(14)15)13-5-6-17(29)20(32)7-13/h5-7,10-11,21,27,29-33,35-36H,8-9H2,1-4H3/t21-,27+/m0/s1InChIKey: KAAFBPHWBXQTAW-KDYSTLNUSA-N
DeepSMILES: COccC)cO)ccc6C=O)CC)C))))O))CccO)cccc6O[C@@H][C@H]C6)O))cccccc6)O))O)))))))))O
Scaffold Graph/Node/Bond level: c1ccc(Cc2cccc3c2OC(c2ccccc2)CC3)cc1
Scaffold Graph/Node level: C1CCC(CC2CCCC3CCC(C4CCCCC4)OC32)CC1
Scaffold Graph level: C1CCC(CC2CCCC3CCC(C4CCCCC4)CC32)CC1
Functional groups: CO; cC(C)=O; cO; cOC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketidesClassyFire Class: Flavonoids
ClassyFire Subclass: Flavans
NP Classifier Biosynthetic pathway: Polyketides|Shikimates and Phenylpropanoids
NP Classifier Superclass: Phloroglucinols|Flavonoids
NP Classifier Class: Dimeric phloroglucinols|Flavan-3-ols
Synonymous chemical names:pilosanol b, pilosanol b+
External chemical identifiers:CID:44257097; ChEMBL:CHEMBL3889597; ZINC:ZINC000014656288
Chemical structure download