ID: ALA2110258

Max Phase: Preclinical

Molecular Formula: C17H25NO3S

Molecular Weight: 323.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)C[C@H](S)[C@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)O

Standard InChI:  InChI=1S/C17H25NO3S/c1-11(2)9-15(22)14(10-13-7-5-4-6-8-13)16(19)18-12(3)17(20)21/h4-8,11-12,14-15,22H,9-10H2,1-3H3,(H,18,19)(H,20,21)/t12-,14-,15-/m0/s1

Standard InChI Key:  YBIZKEFULFLDEE-QEJZJMRPSA-N

Associated Targets(Human)

Angiotensin-converting enzyme 1423 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Neprilysin 341 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: 323.46Molecular Weight (Monoisotopic): 323.1555AlogP: 2.78#Rotatable Bonds: 8
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.23CX Basic pKa: CX LogP: 3.60CX LogD: 0.58
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.64Np Likeness Score: 0.11

References

1. Gomez-Monterrey I, Turcaud S, Lucas E, Bruetschy L, Roques BP, Fournié-Zaluski MC..  (1993)  Exploration of neutral endopeptidase active site by a series of new thiol-containing inhibitors.,  36  (1): [PMID:8421293] [10.1021/jm00053a011]

Source