ID: ALA1908023

Max Phase: Preclinical

Molecular Formula: C20H12O

Molecular Weight: 268.31

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 5-Hydroxybenzo[A]Pyrene
Synonyms from Alternative Forms(1):

    Canonical SMILES:  Oc1cc2cccc3ccc4c5ccccc5cc1c4c32

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

    Standard InChI Key:  ZQOKZAPJXRMEJW-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: 9.30CX Basic pKa: CX LogP: 4.97CX LogD: 4.96
    Aromatic Rings: 5Heavy Atoms: 21QED Weighted: 0.29Np Likeness Score: 0.48

    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