ID: ALA3248061

Max Phase: Preclinical

Molecular Formula: C28H40ClNO2

Molecular Weight: 458.09

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C28H40ClNO2/c1-19(2)30-17-23(31)18-32-26-24(27(3,4)5)15-21(16-25(26)28(6,7)8)10-9-20-11-13-22(29)14-12-20/h9-16,19,23,30-31H,17-18H2,1-8H3/b10-9+

Standard InChI Key:  JBNCEDQGSNBLSO-MDZDMXLPSA-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: 458.09Molecular Weight (Monoisotopic): 457.2748AlogP: 6.84#Rotatable Bonds: 8
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: 7.63CX LogD: 5.40
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.43Np Likeness Score: -0.25

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