ID: ALA129158

Max Phase: Preclinical

Molecular Formula: C24H27NO2

Molecular Weight: 361.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(/C=C2\C(C)=C(CCN3CCOCC3)c3ccccc32)cc1

Standard InChI:  InChI=1S/C24H27NO2/c1-18-21(11-12-25-13-15-27-16-14-25)22-5-3-4-6-23(22)24(18)17-19-7-9-20(26-2)10-8-19/h3-10,17H,11-16H2,1-2H3/b24-17+

Standard InChI Key:  RRIVHTQLWXZTQY-JJIBRWJFSA-N

Associated Targets(non-human)

Prostaglandin-H2 D-isomerase 67 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cannabinoid receptor 174 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: 361.49Molecular Weight (Monoisotopic): 361.2042AlogP: 4.75#Rotatable Bonds: 5
Polar Surface Area: 21.70Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.44CX LogP: 4.27CX LogD: 3.95
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.77Np Likeness Score: -0.70

References

1. Kumar V, Alexander MD, Bell MR, Eissenstat MA, Casiano FM, Chippari SM, Haycock DA, Luttinger DA, Kuster JE, Miller MS, Stevenson JI, Ward SJ.  (1995)  Morpholinoalkylindenes as antinociceptive agents: Novel cannabinoid receptor agonists,  (4): [10.1016/0960-894X(95)00040-Z]

Source