ID: ALA2335501

Max Phase: Preclinical

Molecular Formula: C19H29ClN6

Molecular Weight: 340.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.c1ccc(CNCCN2CCNCc3cccc(n3)CNCC2)nc1

Standard InChI:  InChI=1S/C19H28N6.ClH/c1-2-7-23-17(4-1)14-20-8-11-25-12-9-21-15-18-5-3-6-19(24-18)16-22-10-13-25;/h1-7,20-22H,8-16H2;1H

Standard InChI Key:  NRBOYQTUJILGFH-UHFFFAOYSA-N

Associated Targets(Human)

Superoxide dismutase 173 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Leishmania braziliensis 1091 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania infantum 5912 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

J774.2 197 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypanosoma cruzi 99888 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vero 26788 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: 340.48Molecular Weight (Monoisotopic): 340.2375AlogP: 0.76#Rotatable Bonds: 5
Polar Surface Area: 65.11Molecular Species: BASEHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.76CX LogP: 0.11CX LogD: -2.58
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.70Np Likeness Score: -1.18

References

1. Marín C, Clares MP, Ramírez-Macías I, Blasco S, Olmo F, Soriano C, Verdejo B, Rosales MJ, Gomez-Herrera D, García-España E, Sánchez-Moreno M..  (2013)  In vitro activity of scorpiand-like azamacrocycle derivatives in promastigotes and intracellular amastigotes of Leishmania infantum and Leishmania braziliensis.,  62  [PMID:23395967] [10.1016/j.ejmech.2013.01.001]
2. Olmo F, Marín C, Clares MP, Blasco S, Albelda MT, Soriano C, Gutiérrez-Sánchez R, Arrebola-Vargas F, García-España E, Sánchez-Moreno M..  (2013)  Scorpiand-like azamacrocycles prevent the chronic establishment of Trypanosoma cruzi in a murine model.,  70  [PMID:24158012] [10.1016/j.ejmech.2013.09.048]

Source