(S)-3-amino-4-(1H-imidazol-4-yl)-1-(4-phenyl)-phenylbutan-2-one dihydrochloride

ID: ALA483668

Chembl Id: CHEMBL483668

PubChem CID: 44307625

Max Phase: Preclinical

Molecular Formula: C19H21Cl2N3O

Molecular Weight: 305.38

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cl.Cl.N[C@@H](Cc1c[nH]cn1)C(=O)Cc1ccc(-c2ccccc2)cc1

Standard InChI:  InChI=1S/C19H19N3O.2ClH/c20-18(11-17-12-21-13-22-17)19(23)10-14-6-8-16(9-7-14)15-4-2-1-3-5-15;;/h1-9,12-13,18H,10-11,20H2,(H,21,22);2*1H/t18-;;/m0../s1

Standard InChI Key:  XSOBBCNDWXDGBF-NTEVMMBTSA-N

Associated Targets(Human)

THP-1 (11052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

hisD Histidinol dehydrogenase (48 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brucella suis (86 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDH Histidinol dehydrogenase (18 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: 305.38Molecular Weight (Monoisotopic): 305.1528AlogP: 2.76#Rotatable Bonds: 6
Polar Surface Area: 71.77Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 13.09CX Basic pKa: 7.54CX LogP: 2.80CX LogD: 2.42
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.74Np Likeness Score: -0.24

References

1. Abdo MR, Joseph P, Boigegrain RA, Liautard JP, Montero JL, Köhler S, Winum JY..  (2007)  Brucella suis histidinol dehydrogenase: synthesis and inhibition studies of a series of substituted benzylic ketones derived from histidine.,  15  (13): [PMID:17481905] [10.1016/j.bmc.2007.04.027]
2. Joseph P, Abdo MR, Boigegrain RA, Montero JL, Winum JY, Köhler S..  (2007)  Targeting of the Brucella suis virulence factor histidinol dehydrogenase by histidinol analogues results in inhibition of intramacrophagic multiplication of the pathogen.,  51  (10): [PMID:17698620] [10.1128/aac.00572-07]
3. Dancer JE, Ford MJ, Hamilton K, Kilkelly M, Lindell SD, O'Mahony MJ, Saville-Stones EA.  (1996)  Synthesis of potent inhibitors of histidinol dehydrogenase,  (17): [10.1016/0960-894X(96)00384-8]

Source