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Leridol

PubChem CID: 10495449

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Compound Synonyms Leridol, CHEBI:185602, LMPK12140199, 5-hydroxy-6-(hydroxymethyl)-7-methoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 76.0
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC(C2CCCCC2)CC2CCCCC12
Np Classifier Class Flavanones
Deep Smiles COccC)cOCCC=O)c6cc%10CO)))O)))))cccccc6
Heavy Atom Count 23.0
Classyfire Class Flavonoids
Scaffold Graph Node Level OC1CC(C2CCCCC2)OC2CCCCC12
Classyfire Subclass O-methylated flavonoids
Isotope Atom Count 0.0
Molecular Complexity 420.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 5-hydroxy-6-(hydroxymethyl)-7-methoxy-8-methyl-2-phenyl-2,3-dihydrochromen-4-one
Veber Rule True
Classyfire Superclass Phenylpropanoids and polyketides
Xlogp 2.6
Gsk 4 400 Rule True
Molecular Formula C18H18O5
Scaffold Graph Node Bond Level O=C1CC(c2ccccc2)Oc2ccccc21
Inchi Key NYMCJKZZZIZEPS-UHFFFAOYSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 3.0
Synonyms leridol
Esol Class Soluble
Functional Groups CO, cC(C)=O, cO, cOC
Compound Name Leridol
Exact Mass 314.115
Formal Charge 0.0
Monoisotopic Mass 314.115
Hydrogen Bond Acceptor Count 5.0
Molecular Weight 314.3
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 1.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C18H18O5/c1-10-17(22-2)12(9-19)16(21)15-13(20)8-14(23-18(10)15)11-6-4-3-5-7-11/h3-7,14,19,21H,8-9H2,1-2H3
Smiles CC1=C2C(=C(C(=C1OC)CO)O)C(=O)CC(O2)C3=CC=CC=C3
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Flavonoids

  • 1. Outgoing r'ship FOUND_IN to/from Petiveria Alliacea (Plant) Rel Props:Reference:ISBN:9780387706375; ISBN:9788172362461