ID: ALA1630012

Max Phase: Preclinical

Molecular Formula: C17H24O3

Molecular Weight: 276.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=CCCCCC/C=C\C(O)C#CC#C[C@H](O)[C@H](C)O

Standard InChI:  InChI=1S/C17H24O3/c1-3-4-5-6-7-8-9-12-16(19)13-10-11-14-17(20)15(2)18/h3,9,12,15-20H,1,4-8H2,2H3/b12-9-/t15-,16?,17-/m0/s1

Standard InChI Key:  BEZRAMBFCSSHHE-JMMLGDITSA-N

Associated Targets(non-human)

Quinone oxidoreductase 288 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: 276.38Molecular Weight (Monoisotopic): 276.1725AlogP: 1.79#Rotatable Bonds: 8
Polar Surface Area: 60.69Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.38CX Basic pKa: CX LogP: 3.07CX LogD: 3.07
Aromatic Rings: 0Heavy Atoms: 20QED Weighted: 0.36Np Likeness Score: 2.44

References

1. Shin D, Yang JE, Lee SB, Nho CW..  (2010)  SAR studies of gymnasterkoreayne derivatives with cancer chemopreventive activities.,  20  (24): [PMID:21050753] [10.1016/j.bmcl.2010.07.066]

Source