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Echioidinin 5-O-glucoside

PubChem CID: 44257610

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Compound Synonyms Echioidinin 5-O-glucoside, 5,2'-Dihydroxy-7-methoxyflavone 5-glucoside, LMPK12110120
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 155.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC(C2CCCCC2)CC2CCCC(CC3CCCCC3)C12
Np Classifier Class Flavones
Deep Smiles OCCO[C@@H]OcccOC))ccc6c=O)cco6)cccccc6O)))))))))))))))))C[C@H][C@@H]6O))O))O
Heavy Atom Count 32.0
Classyfire Class Flavonoids
Scaffold Graph Node Level OC1CC(C2CCCCC2)OC2CCCC(OC3CCCCO3)C12
Classyfire Subclass Flavonoid glycosides
Isotope Atom Count 0.0
Molecular Complexity 698.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 3.0
Iupac Name 2-(2-hydroxyphenyl)-7-methoxy-5-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Veber Rule False
Classyfire Superclass Phenylpropanoids and polyketides
Xlogp 0.6
Gsk 4 400 Rule False
Molecular Formula C22H22O10
Scaffold Graph Node Bond Level O=c1cc(-c2ccccc2)oc2cccc(OC3CCCCO3)c12
Inchi Key KDNHFIDMSOTHOV-BLQBXXAQSA-N
Silicos It Class Soluble
Rotatable Bond Count 5.0
Synonyms echioidinin 5-o-glucoside
Esol Class Soluble
Functional Groups CO, c=O, cO, cOC, cO[C@@H](C)OC, coc
Compound Name Echioidinin 5-O-glucoside
Exact Mass 446.121
Formal Charge 0.0
Monoisotopic Mass 446.121
Hydrogen Bond Acceptor Count 10.0
Molecular Weight 446.4
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C22H22O10/c1-29-10-6-15-18(13(25)8-14(30-15)11-4-2-3-5-12(11)24)16(7-10)31-22-21(28)20(27)19(26)17(9-23)32-22/h2-8,17,19-24,26-28H,9H2,1H3/t17?,19-,20+,21?,22-/m1/s1
Smiles COC1=CC2=C(C(=C1)O[C@H]3C([C@H]([C@@H](C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC=CC=C4O
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Flavonoids