ID: ALA4437337

Max Phase: Preclinical

Molecular Formula: C12H9ClN2O

Molecular Weight: 232.67

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1ccncc1)c1cccc(Cl)c1

Standard InChI:  InChI=1S/C12H9ClN2O/c13-10-3-1-2-9(8-10)12(16)15-11-4-6-14-7-5-11/h1-8H,(H,14,15,16)

Standard InChI Key:  AGEMHBDIONALQA-UHFFFAOYSA-N

Associated Targets(non-human)

Ferriprotoporphyrin IX 165 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 232.67Molecular Weight (Monoisotopic): 232.0403AlogP: 2.99#Rotatable Bonds: 2
Polar Surface Area: 41.99Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.62CX LogP: 2.45CX LogD: 2.45
Aromatic Rings: 2Heavy Atoms: 16QED Weighted: 0.87Np Likeness Score: -2.05

References

1. Wicht KJ, Combrinck JM, Smith PJ, Hunter R, Egan TJ..  (2016)  Identification and SAR Evaluation of Hemozoin-Inhibiting Benzamides Active against Plasmodium falciparum.,  59  (13): [PMID:27299916] [10.1021/acs.jmedchem.6b00719]

Source