ID: ALA4204541

Max Phase: Preclinical

Molecular Formula: C23H21ClN4S

Molecular Weight: 420.97

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N#Cc1ccc2c(CNCCCCNc3ccnc4cc(Cl)ccc34)csc2c1

Standard InChI:  InChI=1S/C23H21ClN4S/c24-18-4-6-20-21(7-10-28-22(20)12-18)27-9-2-1-8-26-14-17-15-29-23-11-16(13-25)3-5-19(17)23/h3-7,10-12,15,26H,1-2,8-9,14H2,(H,27,28)

Standard InChI Key:  AUEYWWQGNYLSDW-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: 420.97Molecular Weight (Monoisotopic): 420.1175AlogP: 5.96#Rotatable Bonds: 8
Polar Surface Area: 60.74Molecular Species: BASEHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.59CX LogP: 4.88CX LogD: 2.48
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.35Np Likeness Score: -1.63

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