SELECTIVE BUTYRYLCHOLINESTERASE INHIBITORS AMONG DIALKYLPHOSPHORAMIDOFLUORIDATES
Supposition of a relationship between blood butyrylcholinesterase (BuChE) activity and its lipid composition was reported in a number of works [1-7]. To check this hypothesis, a search of selective BuChE inhibitors among substituted cyclohexyl ester N,N-dialkylphosphoramidofluoridic acids has been a...
Saved in:
Published in | Phosphorus and sulfur and the related elements Vol. 130; no. 1; pp. 115 - 129 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
READING
Taylor & Francis Group
01.11.1997
Taylor & Francis |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Supposition of a relationship between blood butyrylcholinesterase (BuChE) activity and its lipid composition was reported in a number of works [1-7]. To check this hypothesis, a search of selective BuChE inhibitors among substituted cyclohexyl ester N,N-dialkylphosphoramidofluoridic acids has been accomplished by us. For synthesis of substances to be investigated, interaction of N,N- dialkylphosphoramidic difluorides with Na and Al derivatives of corresponding alcohols was used. Investigation of purified, water soluble preparations of BuChE and acetylcholinesterase (AChE) indicated that there were high selective BuChE inhibitors among the investigated compounds. In particular, for N,N-diethyl-O-(trans-2-piperidinocyclohexyl)phosphoramidofluoridate, the reaction constants for cholinesterase inhibition were: k
0
BuChE
= 1,4 × 10
8
M
−1
× min
−1
, k
0
AChE
= 2,1 × 10
4
M
−1
× min
−1
and for its derivative, 1-(trans-2-N,N-diethylamidofluorophosphoryloxycyclohexyl)-1-methylpiperidinium iodide k
0
BuChE
= 2,6 × 10
7
M
−1
× min
−1
, while the AChE inhibition by that compound was reversible (K
i
= 9.8 × 10
−6
M). |
---|---|
ISSN: | 1042-6507 0308-664X 1563-5325 |
DOI: | 10.1080/10426509708033703 |