ID: ALA5291235

Max Phase: Preclinical

Molecular Formula: C18H15NO6

Molecular Weight: 341.32

Associated Items:

Representations

Canonical SMILES:  CC(=O)c1c(O)c(C)c(O)c2c1OC1=Cc3onc(C)c3C(=O)[C@@]12C

Standard InChI:  InChI=1S/C18H15NO6/c1-6-14(21)12(8(3)20)16-13(15(6)22)18(4)10(24-16)5-9-11(17(18)23)7(2)19-25-9/h5,21-22H,1-4H3/t18-/m0/s1

Standard InChI Key:  PYCLUZIYUBSSGD-SFHVURJKSA-N

Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C8 Tchem Cytochrome P450 2C8 (1492 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 341.32Molecular Weight (Monoisotopic): 341.0899AlogP: 2.79#Rotatable Bonds: 1
Polar Surface Area: 109.86Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.53CX Basic pKa: 0.35CX LogP: 1.92CX LogD: 1.68
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.77Np Likeness Score: 1.27

References

1. Gunawan GA, Gimła M, Gardiner MG, Herman-Antosiewicz A, Reekie TA..  (2023)  Divergent reactivity of usnic acid and evaluation of its derivatives for antiproliferative activity against cancer cells.,  79  [PMID:36652792] [10.1016/j.bmc.2023.117157]

Source