ID: ALA3585792

Max Phase: Preclinical

Molecular Formula: C19H24ClN3O3

Molecular Weight: 377.87

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCc1nc(Cl)c(C(=O)N[C@@H](Cc2ccccc2)C(=O)OC)n1C

Standard InChI:  InChI=1S/C19H24ClN3O3/c1-4-5-11-15-22-17(20)16(23(15)2)18(24)21-14(19(25)26-3)12-13-9-7-6-8-10-13/h6-10,14H,4-5,11-12H2,1-3H3,(H,21,24)/t14-/m0/s1

Standard InChI Key:  YSPAKWMWSFPXDS-AWEZNQCLSA-N

Associated Targets(non-human)

Angiotensin-converting enzyme 2863 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: 377.87Molecular Weight (Monoisotopic): 377.1506AlogP: 2.93#Rotatable Bonds: 8
Polar Surface Area: 73.22Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.54CX Basic pKa: 2.83CX LogP: 3.46CX LogD: 3.46
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.72Np Likeness Score: -0.75

References

1. Jallapally A, Addla D, Bagul P, Sridhar B, Banerjee SK, Kantevari S..  (2015)  Design, synthesis and evaluation of novel 2-butyl-4-chloroimidazole derived peptidomimetics as Angiotensin Converting Enzyme (ACE) inhibitors.,  23  (13): [PMID:25922179] [10.1016/j.bmc.2015.04.024]

Source