ID: ALA3276371

Max Phase: Preclinical

Molecular Formula: C19H22ClNO7

Molecular Weight: 321.80

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)C(=O)O.OC(CNCCOc1ccccc1)COc1ccccc1Cl

Standard InChI:  InChI=1S/C17H20ClNO3.C2H2O4/c18-16-8-4-5-9-17(16)22-13-14(20)12-19-10-11-21-15-6-2-1-3-7-15;3-1(4)2(5)6/h1-9,14,19-20H,10-13H2;(H,3,4)(H,5,6)

Standard InChI Key:  OGSNTSZQAZWCJS-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: 321.80Molecular Weight (Monoisotopic): 321.1132AlogP: 2.75#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: 3.07CX LogD: 1.68
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.70Np Likeness Score: -0.96

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