ID: ALA2347837

Max Phase: Preclinical

Molecular Formula: C11H7ClO5

Molecular Weight: 254.62

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)c1ccc(Oc2ccc(Cl)cc2O)o1

Standard InChI:  InChI=1S/C11H7ClO5/c12-6-1-2-8(7(13)5-6)16-10-4-3-9(17-10)11(14)15/h1-5,13H,(H,14,15)

Standard InChI Key:  GTKUURARXBEOSA-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: 254.62Molecular Weight (Monoisotopic): 253.9982AlogP: 3.13#Rotatable Bonds: 3
Polar Surface Area: 79.90Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.13CX Basic pKa: CX LogP: 2.58CX LogD: -1.11
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.88Np Likeness Score: 0.01

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