K727

General

Type : Oxime, Bispyridinium, Bisoxime, Pyridine-aldoxime

Chemical_Nomenclature : naphtylene-2,7-diyl-bis(2-hydroxy-iminomethylpyridinium) dibromide

Canonical SMILES : C1(=CC=[N+](C=C1)CC2=CC3=C(C=C2)C=CC(=C3)C[N+]4=CC=C(C=C4)C(=NO[H])[H])C(=NO[H])[H].[Br-].[Br-]

InChI : InChI=1S\/C24H20N4O2.2BrH\/c29-25-15-19-5-9-27(10-6-19)17-21-1-3-23-4-2-22(14-24(23)13-21)18-28-11-7-20(8-12-28)16-26-30\;\;\/h1-16H,17-18H2\;2*1H

InChIKey : DAKMWEHNZTZIIV-UHFFFAOYSA-N

Other name(s) : K-727


MW : 558.27

Formula : C24H22Br2N4O2

CAS_number :

PubChem :

UniChem : DAKMWEHNZTZIIV-UHFFFAOYSA-N

Target

Structure : No structure

Families : No family

References (2)

Title : Reactivation potency of two novel oximes (K456 and K733) against paraoxon-inhibited acetyl and butyrylcholinesterase: In silico and in vitro models - Iqbal_2019_Chem.Biol.Interact_13ChEPon_310_108735
Author(s) : Iqbal A , Malik S , Nurulain SM , Musilek K , Kuca K , Kalasz H , Fatmi MQ
Ref : Chemico-Biological Interactions , 310 :108735 , 2019
Abstract :
PubMedSearch : Iqbal_2019_Chem.Biol.Interact_13ChEPon_310_108735
PubMedID: 31276662

Title : A comparison of the reactivating and therapeutic efficacy of two novel bispyridinium oximes (K727, K733) with the oxime HI-6 and obidoxime in sarin-poisoned rats and mice - Kassa_2015_Toxicol.Mech.Methods_25_229
Author(s) : Kassa J , Sepsova V , Matouskova L , Horova A , Musilek K
Ref : Toxicol Mech Methods , 25 :229 , 2015
Abstract :
PubMedSearch : Kassa_2015_Toxicol.Mech.Methods_25_229
PubMedID: 25894563