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3'-Angeloyloxy-4',6'-dihydroxy-2',5'-dimethoxychalcone

PubChem CID: 42607633

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Compound Synonyms 3'-Angeloyloxy-4',6'-dihydroxy-2',5'-dimethoxychalcone, CHEBI:178245, LMPK12120356, [2,4-dihydroxy-3,6-dimethoxy-5-[(E)-3-phenylprop-2-enoyl]phenyl] (Z)-2-methylbut-2-enoate, 129724-40-9
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 102.0
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC(CCC1CCCCC1)C1CCCCC1
Np Classifier Class Chalcones
Deep Smiles C/C=CC=O)OccOC))cC=O)/C=C/cccccc6)))))))))ccc6O))OC)))O)))))))/C
Heavy Atom Count 29.0
Classyfire Class Linear 1,3-diarylpropanoids
Scaffold Graph Node Level OC(CCC1CCCCC1)C1CCCCC1
Classyfire Subclass Chalcones and dihydrochalcones
Isotope Atom Count 0.0
Molecular Complexity 621.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name [2,4-dihydroxy-3,6-dimethoxy-5-[(E)-3-phenylprop-2-enoyl]phenyl] (Z)-2-methylbut-2-enoate
Veber Rule True
Classyfire Superclass Phenylpropanoids and polyketides
Xlogp 4.4
Gsk 4 400 Rule True
Molecular Formula C22H22O7
Scaffold Graph Node Bond Level O=C(C=Cc1ccccc1)c1ccccc1
Inchi Key VAKBZJXPGKSDQT-BDVHTTMESA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 8.0
Synonyms angelafolone
Esol Class Moderately soluble
Functional Groups c/C=C/C(c)=O, cO, cOC, cOC(=O)/C(C)=CC
Compound Name 3'-Angeloyloxy-4',6'-dihydroxy-2',5'-dimethoxychalcone
Exact Mass 398.137
Formal Charge 0.0
Monoisotopic Mass 398.137
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 398.4
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 0.0
Total Bond Stereocenter Count 2.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C22H22O7/c1-5-13(2)22(26)29-21-18(25)20(28-4)17(24)16(19(21)27-3)15(23)12-11-14-9-7-6-8-10-14/h5-12,24-25H,1-4H3/b12-11+,13-5-
Smiles C/C=C(/C)\C(=O)OC1=C(C(=C(C(=C1O)OC)O)C(=O)/C=C/C2=CC=CC=C2)OC
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 2.0
Egan Rule True
Np Classifier Superclass Flavonoids