ID: ALA5270105

Max Phase: Preclinical

Molecular Formula: C15H17N5

Molecular Weight: 267.34

Associated Items:

Representations

Canonical SMILES:  CN(C)c1ccc2cc(-c3nccn3C)c(N)nc2c1

Standard InChI:  InChI=1S/C15H17N5/c1-19(2)11-5-4-10-8-12(14(16)18-13(10)9-11)15-17-6-7-20(15)3/h4-9H,1-3H3,(H2,16,18)

Standard InChI Key:  HRXRYAWADPPSLY-UHFFFAOYSA-N

Associated Targets(non-human)

Leishmania mexicana 936 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

J774.A1 2436 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 267.34Molecular Weight (Monoisotopic): 267.1484AlogP: 2.28#Rotatable Bonds: 2
Polar Surface Area: 59.97Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.15CX LogP: 2.13CX LogD: 1.94
Aromatic Rings: 3Heavy Atoms: 20QED Weighted: 0.77Np Likeness Score: -1.23

References

1. Hammill JT, Sviripa VM, Kril LM, Ortiz D, Fargo CM, Kim HS, Chen Y, Rector J, Rice AL, Domagalska MA, Begley KL, Liu C, Rangnekar VM, Dujardin JC, Watt DS, Landfear SM, Guy RK..  (2021)  Amino-Substituted 3-Aryl- and 3-Heteroarylquinolines as Potential Antileishmanial Agents.,  64  (16.0): [PMID:34355566] [10.1021/acs.jmedchem.1c00813]

Source