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CID 42607953

PubChem CID: 42607953

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Compound Synonyms Puddumin B, LMPK12140340
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)CC2CC(CC3CCCCC3)CCC12
Np Classifier Class Flavanones
Deep Smiles OC[C@H]O[C@@H]OcccOCCC=O)c6cc%10)O)))))cccccc6))OC))))))))))))[C@@H][C@H][C@H]6O))O))O
Heavy Atom Count 32.0
Classyfire Class Flavonoids
Scaffold Graph Node Level OC1CC(C2CCCCC2)OC2CC(OC3CCCCO3)CCC12
Classyfire Subclass Flavonoid glycosides
Isotope Atom Count 0.0
Molecular Complexity 638.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name 5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
Veber Rule False
Classyfire Superclass Phenylpropanoids and polyketides
Xlogp 0.9
Gsk 4 400 Rule False
Molecular Formula C22H24O10
Scaffold Graph Node Bond Level O=C1CC(c2ccccc2)Oc2cc(OC3CCCCO3)ccc21
Inchi Key KEEWIHDTSNESJZ-YPSRJAKZSA-N
Silicos It Class Soluble
Rotatable Bond Count 5.0
Synonyms puddumin b, puddumin b(naringenin-4'-methylether-7-o-β-d-galactoside)
Esol Class Soluble
Functional Groups CO, cC(C)=O, cO, cOC, cO[C@@H](C)OC
Compound Name CID 42607953
Exact Mass 448.137
Formal Charge 0.0
Monoisotopic Mass 448.137
Hydrogen Bond Acceptor Count 10.0
Molecular Weight 448.4
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 6.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C22H24O10/c1-29-11-4-2-10(3-5-11)15-8-14(25)18-13(24)6-12(7-16(18)31-15)30-22-21(28)20(27)19(26)17(9-23)32-22/h2-7,15,17,19-24,26-28H,8-9H2,1H3/t15?,17-,19+,20+,21-,22-/m1/s1
Smiles COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)O
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Flavonoids

  • 1. Outgoing r'ship FOUND_IN to/from Prunus Cerasoides (Plant) Rel Props:Reference:ISBN:9788171360536