ID: ALA1908000

Max Phase: Preclinical

Molecular Formula: C20H12O

Molecular Weight: 268.31

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 10-Hydroxybenzo[A]Pyrene
Synonyms from Alternative Forms(1):

    Canonical SMILES:  Oc1cccc2cc3ccc4cccc5ccc(c12)c3c45

    Standard InChI:  InChI=1S/C20H12O/c21-17-6-2-5-14-11-15-8-7-12-3-1-4-13-9-10-16(19(14)17)20(15)18(12)13/h1-11,21H

    Standard InChI Key:  ANHMWNGBSJFXSA-UHFFFAOYSA-N

    Associated Targets(Human)

    UDP-glucuronosyltransferase 1-10 257 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    UDP-glucuronosyltransferase 1-6 221 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    UDP-glucuronosyltransferase 1-8 233 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    UDP-glucuronosyltransferase 2B7 787 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Molecule Features

    Natural Product: YesOral: NoChemical Probe: NoParenteral: No
    Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
    Chirality: NoAvailability: NoProdrug: No

    Drug Indications

    MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

    Mechanisms of Action

    Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

    Properties

    Molecular Weight: 268.31Molecular Weight (Monoisotopic): 268.0888AlogP: 5.44#Rotatable Bonds: 0
    Polar Surface Area: 20.23Molecular Species: NEUTRALHBA: 1HBD: 1
    #RO5 Violations: 1HBA (Lipinski): 1HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
    CX Acidic pKa: 9.43CX Basic pKa: CX LogP: 4.97CX LogD: 4.97
    Aromatic Rings: 5Heavy Atoms: 21QED Weighted: 0.29Np Likeness Score: 0.56

    References

    1. Tukey RH, Strassburg CP..  (2000)  Human UDP-glucuronosyltransferases: metabolism, expression, and disease.,  40  (1): [PMID:10836148] [10.1146/annurev.pharmtox.40.1.581]

    Source