ID: ALA3585801

Max Phase: Preclinical

Molecular Formula: C13H20ClN3O4

Molecular Weight: 317.77

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C13H20ClN3O4/c1-4-5-6-8-15-11(14)10(17(8)3)12(19)16-9(7(2)18)13(20)21/h7,9,18H,4-6H2,1-3H3,(H,16,19)(H,20,21)/t7-,9-/m0/s1

Standard InChI Key:  GWBVYMMMYNUKSV-CBAPKCEASA-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: 317.77Molecular Weight (Monoisotopic): 317.1142AlogP: 0.98#Rotatable Bonds: 7
Polar Surface Area: 104.45Molecular Species: ACIDHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.53CX Basic pKa: 2.57CX LogP: 0.56CX LogD: -2.40
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.70Np Likeness Score: -0.70

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