ID: ALA3277275

Max Phase: Preclinical

Molecular Formula: C21H27NO7S

Molecular Weight: 347.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(C[S+]([O-])c1ccccc1)NCC(O)COc1ccccc1.O=C(O)C(=O)O

Standard InChI:  InChI=1S/C19H25NO3S.C2H2O4/c1-19(2,15-24(22)18-11-7-4-8-12-18)20-13-16(21)14-23-17-9-5-3-6-10-17;3-1(4)2(5)6/h3-12,16,20-21H,13-15H2,1-2H3;(H,3,4)(H,5,6)

Standard InChI Key:  LAGQSUCGOJTKBN-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: 347.48Molecular Weight (Monoisotopic): 347.1555AlogP: 2.60#Rotatable Bonds: 9
Polar Surface Area: 64.55Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.52CX LogP: 2.21CX LogD: 1.06
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.68Np Likeness Score: -0.41

References

1. Tucker H, Coope JF..  (1978)  beta-Adrenergic blocking agents. 18. 1-(Aryloxy)-3-(arylthioalkylamino)propan-2-ols and 1-substituted alkylthioamino-3-(aryloxy)propan-2-ols.,  21  (8): [PMID:29123] [10.1021/jm00206a010]

Source