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Eruberin C

PubChem CID: 44257140

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Compound Synonyms Eruberin C, CHEBI:169773, LMPK12020172, (3S,4S,6S)-2-(hydroxymethyl)-6-[[(2R,4S)-4-methoxy-2-(4-methoxyphenyl)-6,8-dimethyl-5-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-7-yl]oxy]oxane-3,4,5-triol
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 226.0
Hydrogen Bond Donor Count 8.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CC2CC(CC3CCCCC3)C3CCC(C4CCCCC4)CC3C2)CC1
Np Classifier Class Flavandiols (Leucoanthocyanidins)
Deep Smiles COcccccc6))[C@H]C[C@H]OC))ccO6)cC)ccc6O[C@@H]OCCO))[C@H][C@@H]C6O))O))O)))))))C))O[C@@H]OCCO))[C@H][C@@H]C6O))O))O
Heavy Atom Count 46.0
Classyfire Class Flavonoids
Scaffold Graph Node Level C1CCC(C2CCC3C(OC4CCCCO4)CC(OC4CCCCO4)CC3O2)CC1
Classyfire Subclass Flavonoid glycosides
Isotope Atom Count 0.0
Molecular Complexity 953.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (3S,4S,6S)-2-(hydroxymethyl)-6-[[(2R,4S)-4-methoxy-2-(4-methoxyphenyl)-6,8-dimethyl-5-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-7-yl]oxy]oxane-3,4,5-triol
Veber Rule False
Classyfire Superclass Phenylpropanoids and polyketides
Xlogp -0.4
Gsk 4 400 Rule False
Molecular Formula C31H42O15
Scaffold Graph Node Bond Level c1ccc(C2CCc3c(OC4CCCCO4)cc(OC4CCCCO4)cc3O2)cc1
Inchi Key MQPDBDMSPVPGHL-FFGMFJLRSA-N
Silicos It Class Soluble
Rotatable Bond Count 9.0
Synonyms eruberin c
Esol Class Soluble
Functional Groups CO, COC, cOC, cO[C@@H](C)OC
Compound Name Eruberin C
Exact Mass 654.252
Formal Charge 0.0
Monoisotopic Mass 654.252
Hydrogen Bond Acceptor Count 15.0
Molecular Weight 654.7
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 12.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C31H42O15/c1-12-27(45-30-25(38)23(36)21(34)18(10-32)43-30)13(2)29(46-31-26(39)24(37)22(35)19(11-33)44-31)20-17(41-4)9-16(42-28(12)20)14-5-7-15(40-3)8-6-14/h5-8,16-19,21-26,30-39H,9-11H2,1-4H3/t16-,17+,18?,19?,21-,22-,23+,24+,25?,26?,30+,31+/m1/s1
Smiles CC1=C2C(=C(C(=C1O[C@H]3C([C@H]([C@@H](C(O3)CO)O)O)O)C)O[C@H]4C([C@H]([C@@H](C(O4)CO)O)O)O)[C@H](C[C@@H](O2)C5=CC=C(C=C5)OC)OC
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Flavonoids