ID: ALA3585791

Max Phase: Preclinical

Molecular Formula: C15H24ClN3O3S

Molecular Weight: 361.90

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C15H24ClN3O3S/c1-5-6-7-11-18-13(16)12(19(11)2)14(20)17-10(8-9-23-4)15(21)22-3/h10H,5-9H2,1-4H3,(H,17,20)/t10-/m0/s1

Standard InChI Key:  VNIVWECYRGUVEE-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: 361.90Molecular Weight (Monoisotopic): 361.1227AlogP: 2.44#Rotatable Bonds: 9
Polar Surface Area: 73.22Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.54CX Basic pKa: 2.83CX LogP: 2.45CX LogD: 2.45
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.68Np Likeness Score: -1.12

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