1,2-dimethyl-3-(2-(4-nitrophenyl)-2-oxoethyl)-1H-benzo[d]imidazol-3-ium

ID: ALA609734

Chembl Id: CHEMBL609734

PubChem CID: 46877458

Max Phase: Preclinical

Molecular Formula: C17H16ClN3O3

Molecular Weight: 310.33

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: SJ000140722 | CHEMBL609734|SJ000140722

Canonical SMILES:  Cc1n(C)c2ccccc2[n+]1CC(=O)c1ccc([N+](=O)[O-])cc1.[Cl-]

Standard InChI:  InChI=1S/C17H16N3O3.ClH/c1-12-18(2)15-5-3-4-6-16(15)19(12)11-17(21)13-7-9-14(10-8-13)20(22)23;/h3-10H,11H2,1-2H3;1H/q+1;/p-1

Standard InChI Key:  FNSQSLPEYCDDHZ-UHFFFAOYSA-M

Associated Targets(non-human)

Plasmodium falciparum (966862 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

Calculated Properties

Molecular Weight: 310.33Molecular Weight (Monoisotopic): 310.1186AlogP: 2.57#Rotatable Bonds: 4
Polar Surface Area: 69.02Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: -1.61CX LogD: -1.61
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.32Np Likeness Score: -0.94

References

1. Guiguemde WA, Shelat AA, Bouck D, Duffy S, Crowther GJ, Davis PH, Smithson DC, Connelly M, Clark J, Zhu F, Jiménez-Díaz MB, Martinez MS, Wilson EB, Tripathi AK, Gut J, Sharlow ER, Bathurst I, El Mazouni F, Fowble JW, Forquer I, McGinley PL, Castro S, Angulo-Barturen I, Ferrer S, Rosenthal PJ, Derisi JL, Sullivan DJ, Lazo JS, Roos DS, Riscoe MK, Phillips MA, Rathod PK, Van Voorhis WC, Avery VM, Guy RK..  (2010)  Chemical genetics of Plasmodium falciparum.,  465  (7296): [PMID:20485428] [10.1038/nature09099]

Source