ID: ALA3248086

Max Phase: Preclinical

Molecular Formula: C26H38ClNO2

Molecular Weight: 432.05

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)NCC(O)COc1c(C(C)(C)C)cc(-c2ccc(Cl)cc2)cc1C(C)(C)C

Standard InChI:  InChI=1S/C26H38ClNO2/c1-17(2)28-15-21(29)16-30-24-22(25(3,4)5)13-19(14-23(24)26(6,7)8)18-9-11-20(27)12-10-18/h9-14,17,21,28-29H,15-16H2,1-8H3

Standard InChI Key:  GXNDQWPATGFJCG-UHFFFAOYSA-N

Associated Targets(Human)

Adrenergic receptor beta 1214 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 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: 432.05Molecular Weight (Monoisotopic): 431.2591AlogP: 6.34#Rotatable Bonds: 7
Polar Surface Area: 41.49Molecular Species: BASEHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.67CX LogP: 6.94CX LogD: 4.71
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.54Np Likeness Score: -0.35

References

1. Cox MT, Jaggers SE, Jones G..  (1978)  Linked Aryl Aryloxypropanolamines as a new class of lipid catabolis agents.,  21  (2): [PMID:621713] [10.1021/jm00200a008]

Source