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N-Benzylpyridinium

General

Type : Pyridine

Chemical_Nomenclature : 1-benzylpyridin-1-ium chloride

Canonical SMILES : C1=CC=C(C=C1)C[N+]2=CC=CC=C2.[Cl-]

InChI : InChI=1S\/C12H12N.ClH\/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13\;\/h1-10H,11H2\;1H\/q+1\;\/p-1

InChIKey : GNPSDJOWGWWXSS-UHFFFAOYSA-M

Other name(s) : 1-Benzylpyridinium chloride,Pyridinium, 1-(phenylmethyl)-, chloride,2876-13-3,1-benzylpyridin-1-ium chloride,Pyridinium, 1-(phenylmethyl)-, chloride (1:1),benzylpyridinium chloride

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MW : 205.68

Formula : C12H12ClN

CAS_number : 2876-13-3

PubChem : 76135

UniChem : GNPSDJOWGWWXSS-UHFFFAOYSA-M

Target

Families : N-Benzylpyridinium ligand of proteins in family
ACHE

References (3)

1. Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors

Title : Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors - Baharloo_2015_Eur.J.Med.Chem_93C_196

Author(s) : Baharloo F , Moslemin MH , Nadri H , Asadipour A , Mahdavi M , Emami S , Firoozpour L , Mohebat R , Shafiee A , Foroumadi A

Ref : Eur Journal of Medicinal Chemistry , 93C :196 , 2015

Abstract : Baharloo_2015_Eur.J.Med.Chem_93C_196

ESTHER : Baharloo_2015_Eur.J.Med.Chem_93C_196

PubMedSearch : Baharloo_2015_Eur.J.Med.Chem_93C_196

PubMedID: 25681712

2. Indolinone-based acetylcholinesterase inhibitors: Synthesis, biological activity and molecular modeling

Title : Indolinone-based acetylcholinesterase inhibitors: Synthesis, biological activity and molecular modeling - Akrami_2014_Eur.J.Med.Chem_84C_375

Author(s) : Akrami H , Mirjalili BF , Khoobi M , Nadri H , Moradi A , Sakhteman A , Emami S , Foroumadi A , Shafiee A

Ref : Eur Journal of Medicinal Chemistry , 84C :375 , 2014

Abstract : Akrami_2014_Eur.J.Med.Chem_84C_375

ESTHER : Akrami_2014_Eur.J.Med.Chem_84C_375

PubMedSearch : Akrami_2014_Eur.J.Med.Chem_84C_375

PubMedID: 25036795

3. Design, synthesis, biological evaluation and docking study of 5-oxo-4,5-dihydropyrano[3,2-c]chromene derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors

Title : Design, synthesis, biological evaluation and docking study of 5-oxo-4,5-dihydropyrano[3,2-c]chromene derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors - Khoobi_2013_Eur.J.Med.Chem_68C_260

Author(s) : Khoobi M , Alipour M , Sakhteman A , Nadri H , Moradi A , Ghandi M , Emami S , Foroumadi A , Shafiee A

Ref : Eur Journal of Medicinal Chemistry , 68C :260 , 2013

Abstract : Khoobi_2013_Eur.J.Med.Chem_68C_260

ESTHER : Khoobi_2013_Eur.J.Med.Chem_68C_260

PubMedSearch : Khoobi_2013_Eur.J.Med.Chem_68C_260

PubMedID: 23988409

Array
(
    [id] => 5838
    [inhibitor] => N-Benzylpyridinium
    [type] => Array
        (
            [0] => Pyridine
        )

    [other_name] => Array
        (
            [0] => 1-Benzylpyridinium chloride
            [1] => Pyridinium, 1-(phenylmethyl)-, chloride
            [2] => 2876-13-3
            [3] => 1-benzylpyridin-1-ium chloride
            [4] => Pyridinium, 1-(phenylmethyl)-, chloride (1:1)
            [5] => benzylpyridinium chloride
        )

    [chemical_nomenclature] => 1-benzylpyridin-1-ium chloride
    [formula] => C12H12ClN
    [cas_number] => 2876-13-3
    [mw] => 205.68
    [pick_me_to_call] => display_script
    [kinetic_parameter] => 
    [paper] => Akrami_2014_Eur.J.Med.Chem_84C_375 || Baharloo_2015_Eur.J.Med.Chem_93C_196 || Khoobi_2013_Eur.J.Med.Chem_68C_260
    [comment] => 
    [gene_locus] => 
    [kin_inhibitor] => 
    [cid] => 76135
    [family] => ACHE
    [inchikey] => GNPSDJOWGWWXSS-UHFFFAOYSA-M
    [canonicalsmiles] => C1=CC=C(C=C1)C[N+]2=CC=CC=C2.[Cl-]
    [inchi] => InChI=1S\/C12H12N.ClH\/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13\;\/h1-10H,11H2\;1H\/q+1\;\/p-1
    [wikipedia] => 
    [iupharlig] => 
    [structure] => 
    [substrate] => 
    [interact_gene_locus] => 
    [mutation] => 
    [comment2] => 
    [extoxnet] => 
    [news] => 
    [theoretical_model] => 
)