1-Methyl-4-naphthalen-1-ylethynyl-pyridinium iodide

ID: ALA262139

Chembl Id: CHEMBL262139

PubChem CID: 21481567

Max Phase: Preclinical

Molecular Formula: C18H14IN

Molecular Weight: 244.32

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C[n+]1ccc(C#Cc2cccc3ccccc23)cc1.[I-]

Standard InChI:  InChI=1S/C18H14N.HI/c1-19-13-11-15(12-14-19)9-10-17-7-4-6-16-5-2-3-8-18(16)17;/h2-8,11-14H,1H3;1H/q+1;/p-1

Standard InChI Key:  WQDRRHXVIUQDHE-UHFFFAOYSA-M

Associated Targets(Human)

CHAT Tchem Choline acetylase (63 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ache Acetylcholinesterase (2577 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

Calculated Properties

Molecular Weight: 244.32Molecular Weight (Monoisotopic): 244.1121AlogP: 3.06#Rotatable Bonds:
Polar Surface Area: 3.88Molecular Species: NEUTRALHBA: HBD:
#RO5 Violations: HBA (Lipinski): 1HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: -0.08CX LogD: -0.08
Aromatic Rings: 3Heavy Atoms: 19QED Weighted: 0.42Np Likeness Score: -0.38

References

1. Gray AP, Platz RD, Henderson TR, Chang TC, Takahashi K, Dretchen KL..  (1988)  Approaches to protection against nerve agent poisoning. (Naphthylvinyl)pyridine derivatives as potential antidotes.,  31  (4): [PMID:3351860] [10.1021/jm00399a022]

Source