ID: ALA3585798

Max Phase: Preclinical

Molecular Formula: C15H24ClN3O3

Molecular Weight: 329.83

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C15H24ClN3O3/c1-5-6-7-11-18-13(16)12(19(11)4)14(20)17-10(15(21)22)8-9(2)3/h9-10H,5-8H2,1-4H3,(H,17,20)(H,21,22)/t10-/m0/s1

Standard InChI Key:  HKXQTLSQKSMUKH-JTQLQIEISA-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: 329.83Molecular Weight (Monoisotopic): 329.1506AlogP: 2.65#Rotatable Bonds: 8
Polar Surface Area: 84.22Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.71CX Basic pKa: 2.68CX LogP: 2.55CX LogD: -0.44
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.77Np Likeness Score: -0.68

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