Inhibition of the plasma cholinesterase variants by pancuronium bromide and some of its analogues
| Autor: | Judith J. Britten, Mary Whittaker |
|---|---|
| Rok vydání: | 1980 |
| Předmět: |
Stereochemistry
Clinical Biochemistry Biochemistry chemistry.chemical_compound medicine Cholinesterases Humans Ammonium Pancuronium Cholinesterase chemistry.chemical_classification Vecuronium Bromide biology Chemistry Biochemistry (medical) Dibucaine Pancuronium bromide Active site General Medicine Affinities Ammonium compounds Enzyme biology.protein Cholinesterase Inhibitors medicine.drug |
| Zdroj: | Clinica chimica acta; international journal of clinical chemistry. 108(1) |
| ISSN: | 0009-8981 |
| Popis: | Pancuronium bromide, a 3,17-diacetoxy-5 alpha-androstane, and three of its analogues, the 17-desoxy, the 3,17-dibutyryloxy and the 16-N-monoquaternary ammonium derivatives have been used as inhibitors of the usual and atypical plasma cholinesterase variants. In all cases the usual enzyme is more sensitive to inhibition by the substituted steroids than the dibucaine resistant enzyme. The relative affinities of the bis-quaternary ammonium compounds for either enzyme is in the order dibutyryloxy derivative17-desoxy derivative greater than or equal to pancuronium bromide. The monoquaternary compound has the least affinity of all the inhibitors for the usual enzyme but the greater affinity for the atypical enzyme. These observations show that the bis-quaternary compounds are very powerful differentiators of the variants. The monoquaternary derivative shows less differential inhibition, but provides additional evidence that the usual and dibucaine resistant variants differ in structure at or near their esteratic active site. |
| Databáze: | OpenAIRE |
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