ID: ALA3248075

Max Phase: Preclinical

Molecular Formula: C26H39NO2S

Molecular Weight: 429.67

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)NCC(O)COc1c(C(C)(C)C)cc(/C=C/c2cccs2)cc1C(C)(C)C

Standard InChI:  InChI=1S/C26H39NO2S/c1-18(2)27-16-20(28)17-29-24-22(25(3,4)5)14-19(15-23(24)26(6,7)8)11-12-21-10-9-13-30-21/h9-15,18,20,27-28H,16-17H2,1-8H3/b12-11+

Standard InChI Key:  MDOSPICFECGVNF-VAWYXSNFSA-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: 429.67Molecular Weight (Monoisotopic): 429.2702AlogP: 6.25#Rotatable Bonds: 8
Polar Surface Area: 41.49Molecular Species: BASEHBA: 4HBD: 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: 0.52Np Likeness Score: -0.68

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