ID: ALA432858

Max Phase: Preclinical

Molecular Formula: C21H16O5

Molecular Weight: 348.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1c2c(O)cccc2Cc2ccc(Cc3ccc(O)cc3O)c(O)c21

Standard InChI:  InChI=1S/C21H16O5/c22-15-7-6-11(17(24)10-15)8-14-5-4-13-9-12-2-1-3-16(23)18(12)21(26)19(13)20(14)25/h1-7,10,22-25H,8-9H2

Standard InChI Key:  WZAVERXTFSLUQU-UHFFFAOYSA-N

Associated Targets(Human)

HaCaT 4069 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Arachidonate 5-lipoxygenase 259 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: 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: 348.35Molecular Weight (Monoisotopic): 348.0998AlogP: 3.24#Rotatable Bonds: 2
Polar Surface Area: 97.99Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.01CX Basic pKa: CX LogP: 5.73CX LogD: 5.18
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.45Np Likeness Score: 1.16

References

1. Müller K, Leukel P, Ziereis K, Gawlik I..  (1994)  Antipsoriatic anthrones with modulated redox properties. 2. Novel derivatives of chrysarobin and isochrysarobin--antiproliferative activity and 5-lipoxygenase inhibition.,  37  (11): [PMID:8201600] [10.1021/jm00037a017]

Source