ID: ALA2347834

Max Phase: Preclinical

Molecular Formula: C17H17ClN2O5

Molecular Weight: 364.79

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)N1CCN(C(=O)c2ccc(Oc3ccc(Cl)cc3O)o2)CC1

Standard InChI:  InChI=1S/C17H17ClN2O5/c1-11(21)19-6-8-20(9-7-19)17(23)15-4-5-16(25-15)24-14-3-2-12(18)10-13(14)22/h2-5,10,22H,6-9H2,1H3

Standard InChI Key:  QDTZYKUZPBBAAH-UHFFFAOYSA-N

Associated Targets(Human)

HFF 3142 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Enoyl-acyl carrier reductase 64 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Toxoplasma gondii 4585 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: 364.79Molecular Weight (Monoisotopic): 364.0826AlogP: 2.74#Rotatable Bonds: 3
Polar Surface Area: 83.22Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.54CX Basic pKa: CX LogP: 1.30CX LogD: 1.06
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.90Np Likeness Score: -0.73

References

1. Cheng G, Muench SP, Zhou Y, Afanador GA, Mui EJ, Fomovska A, Lai BS, Prigge ST, Woods S, Roberts CW, Hickman MR, Lee PJ, Leed SE, Auschwitz JM, Rice DW, McLeod R..  (2013)  Design, synthesis, and biological activity of diaryl ether inhibitors of Toxoplasma gondii enoyl reductase.,  23  (7): [PMID:23453069] [10.1016/j.bmcl.2013.02.019]

Source