ID: ALA2380419

Max Phase: Preclinical

Molecular Formula: C22H25NO3

Molecular Weight: 351.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCn1cc(C(=O)Cc2ccc(OC)cc2)c2cccc(OC)c21

Standard InChI:  InChI=1S/C22H25NO3/c1-4-5-13-23-15-19(18-7-6-8-21(26-3)22(18)23)20(24)14-16-9-11-17(25-2)12-10-16/h6-12,15H,4-5,13-14H2,1-3H3

Standard InChI Key:  QHRAKHVQVUFVRP-UHFFFAOYSA-N

Associated Targets(Human)

Cannabinoid CB2 receptor 16942 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cannabinoid CB1 receptor 739 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cannabinoid CB2 receptor 862 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: 351.45Molecular Weight (Monoisotopic): 351.1834AlogP: 4.88#Rotatable Bonds: 8
Polar Surface Area: 40.46Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.70CX LogD: 4.70
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.54Np Likeness Score: -0.58

References

1. Vasiljevik T, Franks LN, Ford BM, Douglas JT, Prather PL, Fantegrossi WE, Prisinzano TE..  (2013)  Design, synthesis, and biological evaluation of aminoalkylindole derivatives as cannabinoid receptor ligands with potential for treatment of alcohol abuse.,  56  (11): [PMID:23631463] [10.1021/jm400268b]

Source