ID: ALA558146

Max Phase: Preclinical

Molecular Formula: C14H14F5NO3S

Molecular Weight: 371.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CC(S)C(F)(F)C(F)(F)F)NC(Cc1ccccc1)C(=O)O

Standard InChI:  InChI=1S/C14H14F5NO3S/c15-13(16,14(17,18)19)10(24)7-11(21)20-9(12(22)23)6-8-4-2-1-3-5-8/h1-5,9-10,24H,6-7H2,(H,20,21)(H,22,23)

Standard InChI Key:  DYMMAGGCPNJADM-UHFFFAOYSA-N

Associated Targets(Human)

Angiotensin-converting enzyme 1423 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Endothelin-converting enzyme 1 674 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Neprilysin 9 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: 371.33Molecular Weight (Monoisotopic): 371.0615AlogP: 2.68#Rotatable Bonds: 7
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.77CX Basic pKa: CX LogP: 2.99CX LogD: -0.30
Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.51Np Likeness Score: -0.21

References

1. Olimpieri F, Tambaro S, Fustero S, Lazzari P, Sanchez-Roselló M, Pani L, Volonterio A, Zanda M..  (2009)  Synthesis and enzymatic evaluation of novel partially fluorinated thiol dual ACE/NEP inhibitors.,  19  (16): [PMID:19596577] [10.1016/j.bmcl.2009.06.064]

Source