N-(2,6-Diisopropyl-phenyl)-malonamic acid 1-methyl-nonyl ester

ID: ALA159666

Chembl Id: CHEMBL159666

PubChem CID: 44375510

Max Phase: Preclinical

Molecular Formula: C25H41NO3

Molecular Weight: 403.61

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCCCC(C)OC(=O)CC(=O)Nc1c(C(C)C)cccc1C(C)C

Standard InChI:  InChI=1S/C25H41NO3/c1-7-8-9-10-11-12-14-20(6)29-24(28)17-23(27)26-25-21(18(2)3)15-13-16-22(25)19(4)5/h13,15-16,18-20H,7-12,14,17H2,1-6H3,(H,26,27)

Standard InChI Key:  CDFOAUATSIBRJO-UHFFFAOYSA-N

Associated Targets(non-human)

ACAT Acyl-CoA:cholesterol acyltransferase (1121 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

Calculated Properties

Molecular Weight: 403.61Molecular Weight (Monoisotopic): 403.3086AlogP: 6.94#Rotatable Bonds: 13
Polar Surface Area: 55.40Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.71CX Basic pKa: CX LogP: 7.70CX LogD: 7.70
Aromatic Rings: 1Heavy Atoms: 29QED Weighted: 0.22Np Likeness Score: -0.12

References

1. Sliskovic D, Picard J, Roark W, Essenburg A, Krause B, Minton L, Reindel J, Stanfield R.  (1996)  Inhibitors of acyl-CoA: cholesterol O-acyl transferase (ACAT) as hypocholesterolemic agents. The synthesis and biological activity of a series of malonester amides,  (6): [10.1016/0960-894X(96)00098-4]

Source