Skip to search formSkip to main contentSkip to account menu

aprofen

Known as: 2,2-diphenylpropanoic acid N,N-diethylaminoethyl ester, 2-diethylaminoethyl 2,2-diphenylpropionate, aprophen 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (2)

ParasympatholyticsPhenylpropionates

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2001
2001
Effects of selected anticholinergics on acoustic startle response in rats
The present study compared the effects of the anticholinergics aprophen hydrochloride, atropine sulfate, azaprophen hydrochloride… 
1992
1992
Muscarinic receptor subtype specificity of (N,N-dialkylamino)alkyl 2-cyclohexyl-2-phenylpropionates: cylexphenes (cyclohexyl-substituted aprophen analogues).
A series of aprophen [(N,N-diethylamino)ethyl 2,2-diphenylpropionate] analogues, called cylexphenes, were synthesized with… 
1991
1991
Physostigmine (alone and together with adjunct) pretreatment against soman, sarin, tabun and VX intoxication.
A pretreatment for organophosphorus (OP) anticholinesterase (e.g., soman) intoxication should prevent lethality and convulsions… 
1991
1991
M1 muscarinic antagonists interact with sigma recognition sites.
The M1-selective muscarinic antagonists aprophen, caramiphen, carbetapentane, 2-DAEX, dicyclomine, hexahydrosiladifenidol… 
1990
1990
Aprophit: an irreversible antagonist for muscarinic receptors.
1986
1986
Disposition of aprophen in rats
The pharmacokinetics of [14C]aprophen and its distribution were determined after intravenous administration to rats. The drug was… 
1986
1986
Kinetic investigations into the interactions of aprophen with cholinesterases and a carboxylesterase.
1986
1986
Enzymatic synthesis of a false cholinergic neurotransmitter: diethylaminoethyl acetate as a muscarinic agonist analog of acetylcholine.
1985
1985
Aprophen: a substrate and inhibitor of butyrylcholinesterase and carboxylesterases.
1983
1983
Antimuscarinic activity of aprophen.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)