4-(2-Anthracen-9-yl-vinyl)-1-methyl-pyridinium iodide

ID: ALA354726

Chembl Id: CHEMBL354726

PubChem CID: 44379725

Max Phase: Preclinical

Molecular Formula: C22H18IN

Molecular Weight: 296.39

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  C[n+]1ccc(/C=C/c2c3ccccc3cc3ccccc23)cc1.[I-]

Standard InChI:  InChI=1S/C22H18N.HI/c1-23-14-12-17(13-15-23)10-11-22-20-8-4-2-6-18(20)16-19-7-3-5-9-21(19)22;/h2-16H,1H3;1H/q+1;/p-1/b11-10+;

Standard InChI Key:  HSARNYRKEYRWGP-ASTDGNLGSA-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: 296.39Molecular Weight (Monoisotopic): 296.1434AlogP: 4.99#Rotatable Bonds: 2
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: 1.13CX LogD: 1.13
Aromatic Rings: 4Heavy Atoms: 23QED Weighted: 0.36Np Likeness Score: 0.09

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