ID: ALA4218066

Max Phase: Preclinical

Molecular Formula: C23H29ClN4O2

Molecular Weight: 428.96

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=[N+]([O-])c1cnc2cc(Cl)ccc2c1NCCCNCC12CC3CC(CC(C3)C1)C2

Standard InChI:  InChI=1S/C23H29ClN4O2/c24-18-2-3-19-20(9-18)27-13-21(28(29)30)22(19)26-5-1-4-25-14-23-10-15-6-16(11-23)8-17(7-15)12-23/h2-3,9,13,15-17,25H,1,4-8,10-12,14H2,(H,26,27)

Standard InChI Key:  NNFVPOIUZNXASR-UHFFFAOYSA-N

Associated Targets(Human)

THP-1 11052 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Leishmania tropica 461 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania infantum 5912 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: 428.96Molecular Weight (Monoisotopic): 428.1979AlogP: 5.40#Rotatable Bonds: 8
Polar Surface Area: 80.09Molecular Species: BASEHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 10.55CX LogP: 4.92CX LogD: 2.03
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.33Np Likeness Score: -0.87

References

1. Konstantinović J, Videnović M, Orsini S, Bogojević K, D'Alessandro S, Scaccabarozzi D, Terzić Jovanović N, Gradoni L, Basilico N, Šolaja BA..  (2018)  Novel Aminoquinoline Derivatives Significantly Reduce Parasite Load in Leishmania infantum Infected Mice.,  (7): [PMID:30034591] [10.1021/acsmedchemlett.8b00053]

Source