ID: ALA3276365

Max Phase: Preclinical

Molecular Formula: C18H24ClNO3

Molecular Weight: 301.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cccc(OCC(O)CNCCOc2ccccc2)c1.Cl

Standard InChI:  InChI=1S/C18H23NO3.ClH/c1-15-6-5-9-18(12-15)22-14-16(20)13-19-10-11-21-17-7-3-2-4-8-17;/h2-9,12,16,19-20H,10-11,13-14H2,1H3;1H

Standard InChI Key:  PNHNHAFPGVEEHR-UHFFFAOYSA-N

Associated Targets(non-human)

Felis catus 3858 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: 301.39Molecular Weight (Monoisotopic): 301.1678AlogP: 2.40#Rotatable Bonds: 9
Polar Surface Area: 50.72Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.77CX LogP: 2.98CX LogD: 1.59
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.70Np Likeness Score: -0.85

References

1. Smith LH, Tucker H..  (1977)  beta-Adrenergic blocking agents. 17. 1-Phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propanols.,  20  (12): [PMID:22750] [10.1021/jm00222a022]

Source