17-desoxypancuronium

Dacuronium, 17-desoxy analog of pancuronium || 17-desoxy analog of pancuronium

General

Type : Nicotinic antagonist,Neuromuscular Nondepolarizing Agents,Not A\/B H target,Acetate,Phenanthrene

Chemical_Nomenclature : [(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-17-hydroxy-10,13-dimethyl-2,16-bis(1-methylpiperidin-1-ium-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

Canonical SMILES : CC(=O)OC1CC2CCC3C(C2(CC1[N+]4(CCCCC4)C)C)CCC5(C3CC(C5O)[N+]6(CCCCC6)C)C

InChI : InChI=1S\/C33H58N2O3\/c1-23(36)38-30-20-24-12-13-25-26(33(24,3)22-29(30)35(5)18-10-7-11-19-35)14-15-32(2)27(25)21-28(31(32)37)34(4)16-8-6-9-17-34\/h24-31,37H,6-22H2,1-5H3\/q+2\/t24-,25+,26-,27-,28-,29-,30-,31-,32-,33-\/m0\/s1

InChIKey : XQFBAGUGBNQLRT-ZZZJANDJSA-N || XQFBAGUGBNQLRT-KEEQEOMKSA-N || SUKULMJPMHYWKC-VMDJIQQCSA-L || SUKULMJPMHYWKC-GMMLHHOXSA-L || SUKULMJPMHYWKC-ASCUVKKQSA-L

Other name(s) : 17-desoxypancuronium,Dacuronium,NB68,UNII-VD6L56ZVX1,AC1L54NO,VD6L56ZVX1,CHEMBL3138543,Org 6368


Target

Families : 17-desoxypancuronium ligand of proteins in family: BCHE

Stucture :

Protein :

References (3)

Title : Genetic variants of human serum cholinesterase influence metabolism of the muscle relaxant succinylcholine. - Lockridge_1990_Pharmacol.Ther_47_35
Author(s) : Lockridge O
Ref : Pharmacol Ther , 47 :35 , 1990
Abstract : Lockridge_1990_Pharmacol.Ther_47_35
ESTHER : Lockridge_1990_Pharmacol.Ther_47_35
PubMedSearch : Lockridge_1990_Pharmacol.Ther_47_35
PubMedID: 2195556
Gene_locus related to this paper: human-BCHE

Title : Differential inhibition of plasma cholinesterase variants using the dibutyrate analogue of pancuronium bromide - Whittaker_1981_Hum.Hered_31_242
Author(s) : Whittaker M , Britten JJ
Ref : Hum Hered , 31 :242 , 1981
Abstract : Whittaker_1981_Hum.Hered_31_242
ESTHER : Whittaker_1981_Hum.Hered_31_242
PubMedSearch : Whittaker_1981_Hum.Hered_31_242
PubMedID: 7287015

Title : The activity of various esterase inhibitors towards atypical human serum cholinesterase -
Author(s) : Kalow W , Davies R0
Ref : Biochemical Pharmacology , 1 :183 , 1958
PubMedID: