ID: ALA4100236

Max Phase: Preclinical

Molecular Formula: C10H13ClN4

Molecular Weight: 224.69

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N=C1NCCN1CCc1ccc(Cl)nc1

Standard InChI:  InChI=1S/C10H13ClN4/c11-9-2-1-8(7-14-9)3-5-15-6-4-13-10(15)12/h1-2,7H,3-6H2,(H2,12,13)

Standard InChI Key:  PIEAMDLDSKJTAA-UHFFFAOYSA-N

Associated Targets(non-human)

Neuronal acetylcholine receptor; alpha3/beta4 1368 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuronal acetylcholine receptor; alpha4/beta2 3557 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: 224.69Molecular Weight (Monoisotopic): 224.0829AlogP: 1.12#Rotatable Bonds: 3
Polar Surface Area: 52.01Molecular Species: BASEHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 11.75CX LogP: 1.03CX LogD: -1.38
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.76Np Likeness Score: -1.09

References

1. Wu J, Cippitelli A, Zhang Y, Debevec G, Schoch J, Ozawa A, Yu Y, Liu H, Chen W, Houghten RA, Welmaker GS, Giulianotti MA, Toll L..  (2017)  Highly Selective and Potent α4β2 nAChR Antagonist Inhibits Nicotine Self-Administration and Reinstatement in Rats.,  60  (24): [PMID:29178785] [10.1021/acs.jmedchem.7b01250]

Source