ID: ALA3276338

Max Phase: Preclinical

Molecular Formula: C14H23NO3

Molecular Weight: 253.34

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOCCCNCC(O)COc1ccccc1

Standard InChI:  InChI=1S/C14H23NO3/c1-2-17-10-6-9-15-11-13(16)12-18-14-7-4-3-5-8-14/h3-5,7-8,13,15-16H,2,6,9-12H2,1H3

Standard InChI Key:  YROKNKAAYLJFLZ-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: 253.34Molecular Weight (Monoisotopic): 253.1678AlogP: 1.44#Rotatable Bonds: 10
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: 9.56CX LogP: 1.19CX LogD: -0.94
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.62Np Likeness Score: -0.82

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