ID: ALA368957

Max Phase: Preclinical

Molecular Formula: C17H16O3

Molecular Weight: 268.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1C(=O)c2ccccc2C2=C1CCC1(CCCC1)O2

Standard InChI:  InChI=1S/C17H16O3/c18-14-11-5-1-2-6-12(11)16-13(15(14)19)7-10-17(20-16)8-3-4-9-17/h1-2,5-6H,3-4,7-10H2

Standard InChI Key:  LAZRBHRYUSKPGR-UHFFFAOYSA-N

Associated Targets(non-human)

Rauscher murine leukemia virus 38 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Avian myeloblastosis virus 26 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: 268.31Molecular Weight (Monoisotopic): 268.1099AlogP: 3.29#Rotatable Bonds: 0
Polar Surface Area: 43.37Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.21CX LogD: 3.21
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.68Np Likeness Score: 1.02

References

1. Schaffner-Sabba K, Schmidt-Ruppin KH, Wehrli W, Schuerch AR, Wasley JW..  (1984)  beta-Lapachone: synthesis of derivatives and activities in tumor models.,  27  (8): [PMID:6205152] [10.1021/jm00374a010]

Source