ID: ALA2058732

Max Phase: Preclinical

Molecular Formula: C17H27NO3

Molecular Weight: 293.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)OCCCCCCCCCCOc1ccccn1

Standard InChI:  InChI=1S/C17H27NO3/c1-16(19)20-14-10-6-4-2-3-5-7-11-15-21-17-12-8-9-13-18-17/h8-9,12-13H,2-7,10-11,14-15H2,1H3

Standard InChI Key:  HIJGWQMBHZQCIR-UHFFFAOYSA-N

Associated Targets(non-human)

Leishmania mexicana 936 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: 293.41Molecular Weight (Monoisotopic): 293.1991AlogP: 4.14#Rotatable Bonds: 12
Polar Surface Area: 48.42Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.92CX LogP: 4.19CX LogD: 4.19
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.43Np Likeness Score: -0.53

References

1. García Liñares G, Parraud G, Labriola C, Baldessari A..  (2012)  Chemoenzymatic synthesis and biological evaluation of 2- and 3-hydroxypyridine derivatives against Leishmania mexicana.,  20  (15): [PMID:22781310] [10.1016/j.bmc.2012.06.028]

Source