Phenyltetrahydroisoquinoline-Pyridinaldoxime-1c

General

Type : Oxime, Pyridine-aldoxime, Isoquinoline

Chemical_Nomenclature : 6-[5-(6,7-dimethoxy-1-phenyl-3,4-dihydro-1H-isoquinolin-2-yl)pentyl]-2-[(E)-hydroxyiminomethyl]pyridin-3-ol

Canonical SMILES : COC1=C(C=C2C(N(CCC2=C1)CCCCCC3=NC(=C(C=C3)O)C=NO)C4=CC=CC=C4)OC

InChI : InChI=1S\/C28H33N3O4\/c1-34-26-17-21-14-16-31(28(20-9-5-3-6-10-20)23(21)18-27(26)35-2)15-8-4-7-11-22-12-13-25(32)24(30-22)19-29-33\/h3,5-6,9-10,12-13,17-19,28,32-33H,4,7-8,11,14-16H2,1-2H3\/b29-19+

InChIKey : OKSPDBSTEZCWNM-VUTHCHCSSA-N

Other name(s) : GM113  ||  CHEMBL2181432


MW : 475.6

Formula : C28H33N3O4

CAS_number :

PubChem : 136015314

UniChem : OKSPDBSTEZCWNM-VUTHCHCSSA-N

Target

Structure : No structure

Families : No family

References (3)

Title : An easy method for the determination of active concentrations of cholinesterase reactivators in blood samples: Application to the efficacy assessment of non quaternary reactivators compared to HI-6 and pralidoxime in VX-poisoned mice - Calas_2017_Chem.Biol.Interact_267_11
Author(s) : Calas AG , Dias J , Rousseau C , Arboleas M , Touvrey-Loiodice M , Mercey G , Jean L , Renard PY , Nachon F
Ref : Chemico-Biological Interactions , 267 :11 , 2017
Abstract :
PubMedSearch : Calas_2017_Chem.Biol.Interact_267_11
PubMedID: 26972668

Title : Phenyltetrahydroisoquinoline-pyridinaldoxime conjugates as efficient uncharged reactivators for the dephosphylation of inhibited human acetylcholinesterase - Mercey_2012_J.Med.Chem_55_10791
Author(s) : Mercey G , Renou J , Verdelet T , Kliachyna M , Baati R , Gillon E , Arboleas M , Loiodice M , Nachon F , Jean L , Renard PY
Ref : Journal of Medicinal Chemistry , 55 :10791 , 2012
Abstract :
PubMedSearch : Mercey_2012_J.Med.Chem_55_10791
PubMedID: 23148598

Title : First efficient uncharged reactivators for the dephosphylation of poisoned human acetylcholinesterase - Mercey_2011_Chem.Commun.(Camb)_47_5295
Author(s) : Mercey G , Verdelet T , Saint-Andre G , Gillon E , Wagner A , Baati R , Jean L , Nachon F , Renard PY
Ref : Chem Commun (Camb) , 47 :5295 , 2011
Abstract :
PubMedSearch : Mercey_2011_Chem.Commun.(Camb)_47_5295
PubMedID: 21451868