(S)-[5-(4-Chloro-2-methoxy-phenyl)-1-methyl-1H-[1,2,4]triazol-3-yl]-[1-(4-fluoro-phenyl)-pentyl]-propyl-amine hydrochloride

ID: ALA2094063

Chembl Id: CHEMBL2094063

PubChem CID: 11306179

Max Phase: Preclinical

Molecular Formula: C24H31Cl2FN4O

Molecular Weight: 444.98

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCC[C@@H](c1ccc(F)cc1)N(CCC)c1nc(-c2ccc(Cl)cc2OC)n(C)n1.Cl

Standard InChI:  InChI=1S/C24H30ClFN4O.ClH/c1-5-7-8-21(17-9-12-19(26)13-10-17)30(15-6-2)24-27-23(29(3)28-24)20-14-11-18(25)16-22(20)31-4;/h9-14,16,21H,5-8,15H2,1-4H3;1H/t21-;/m0./s1

Standard InChI Key:  VOFYECVPKIYSMX-BOXHHOBZSA-N

Associated Targets(Human)

CRHR1 Tclin Corticotropin releasing factor receptor 1 (2996 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Crhr2 Corticotropin releasing factor receptor (165 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

Calculated Properties

Molecular Weight: 444.98Molecular Weight (Monoisotopic): 444.2092AlogP: 6.43#Rotatable Bonds: 10
Polar Surface Area: 43.18Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 1.04CX LogP: 7.55CX LogD: 7.55
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.36Np Likeness Score: -1.09

References

1. Lowe RF, Nelson J, Dang TN, Crowe PD, Pahuja A, McCarthy JR, Grigoriadis DE, Conlon P, Saunders J, Chen C, Szabo T, Chen TK, Bozigian H..  (2005)  Rational design, synthesis, and structure-activity relationships of aryltriazoles as novel corticotropin-releasing factor-1 receptor antagonists.,  48  (5): [PMID:15743196] [10.1021/jm049339c]

Source