ID: ALA1203140

Max Phase: Preclinical

Molecular Formula: C20H26ClN3O4

Molecular Weight: 371.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccccc1N1CCN(CC(O)c2ccc(O)c(C(N)=O)c2)CC1.Cl

Standard InChI:  InChI=1S/C20H25N3O4.ClH/c1-27-19-5-3-2-4-16(19)23-10-8-22(9-11-23)13-18(25)14-6-7-17(24)15(12-14)20(21)26;/h2-7,12,18,24-25H,8-11,13H2,1H3,(H2,21,26);1H

Standard InChI Key:  BWIWGOAPWLFLKA-UHFFFAOYSA-N

Associated Targets(Human)

Adrenergic receptor alpha-1 948 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Adrenergic receptor beta 1214 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cavia porcellus 23802 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rattus norvegicus 775804 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: 371.44Molecular Weight (Monoisotopic): 371.1845AlogP: 1.36#Rotatable Bonds: 6
Polar Surface Area: 99.26Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.21CX Basic pKa: 7.21CX LogP: 1.76CX LogD: 1.76
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.71Np Likeness Score: -0.96

References

1. Grisar JM, Claxton GP, Bare TM, Dage RC, Cheng HC, Woodward JK..  (1981)  Salicylamide derivatives related to medroxalol with alpha- and beta-adrenergic antagonist and antihypertension activity.,  24  (3): [PMID:6115059] [10.1021/jm00135a017]

Source