N1-(3-(2-benzyl-4-chlorophenoxy)propyl)-N2,N2-dimethylethane-1,2-diamine

ID: ALA589427

Chembl Id: CHEMBL589427

PubChem CID: 45489392

Max Phase: Preclinical

Molecular Formula: C20H28Cl2N2O

Molecular Weight: 346.90

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Synonyms: SJ000198684 | CHEMBL589427|SJ000198684

Canonical SMILES:  CN(C)CCNCCCOc1ccc(Cl)cc1Cc1ccccc1.Cl

Standard InChI:  InChI=1S/C20H27ClN2O.ClH/c1-23(2)13-12-22-11-6-14-24-20-10-9-19(21)16-18(20)15-17-7-4-3-5-8-17;/h3-5,7-10,16,22H,6,11-15H2,1-2H3;1H

Standard InChI Key:  INYFPEHJRXKMST-UHFFFAOYSA-N

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: 346.90Molecular Weight (Monoisotopic): 346.1812AlogP: 3.85#Rotatable Bonds: 10
Polar Surface Area: 24.50Molecular Species: BASEHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.78CX LogP: 4.23CX LogD: 1.87
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.66Np Likeness Score: -0.96

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