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valproate phenacyl ester

Known as: phenacyl valproate 
National Institutes of Health

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Valproic Acid
analogs & derivatives

Papers overview

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2014
2014
Mechanistic Studies on Alcoholysis of α-Keto esters
In the course of our studies on the solvent effect inphotochemistry of phenacyl carboxylates, we had a chanceto prepare and work… 
2006
2006
Novel N-(2,2-Dimethyl-2H-azirin-3-yl)-L-prolinates as Aib-Pro Synthons
The syntheses of phenacyl N-(2,2-dimethyl-2H-azirin-3-yl)-L-prolinate and allyl N-(2,2-dimethyl-2H-azirin-3-yl)-L-prolinate are… 
2005
2005
Neurochemical estimations of some new quaternary phenacyl-bromopiperidinium compounds.
Considering the fact that N-alkyl substituted quaternary ammonium salts of piperidinium bromide induce brain catecholamine and… 
2000
2000
Synthesis of 3-Substituted Phenacyl-5-[2-phenyl-4H-4-oxo-1-benzopyran-6-yl)methylenyl]-thiazolidine-2,4-diones and Evaluation of Their Antimicrobial Activity
Summary Synthesis and physico-chemical properties of two 3-substituted phenacyl-thiazolidine-2,4-di-ones (2c-d) and four 3… 
1998
1998
Mechanism of neuromuscular blockade induced by phenthonium, a quaternary derivative of (−)–hyoscyamine, in skeletal muscles
1 The mechanisms underlying the postjunctional blockade induced by phenthonium [N‐(4‐phenyl) phenacyl 1‐hyoscyamine] were… 
1995
1995
Recent advances of chemiluminescent and bioluminescent assay
Recently, chemiluminescence (CL) and bioluminescence (BL) assays are attractive analytical method in the field of clinical… 
1994
1994
Enantioselective and reversible inhibition of trypsin and alpha-chymotrypsin by phosphonate esters.
Trypsin is inactivated by the levorotatory enantiomers (most likely PS) of 4-nitrophenyl 4-H-, 4-CH3-,4-OCH3-, and 4-Cl-phenacyl… 
1987
1987
Studies on the Quaternization of Tertiary Amine (V). The Quaternization of Pyridine with Phenacyl Arenesulfonates
The effect of substituent inleaving group on the rates of reactions of phenacyl substituted-benzenesulfonates with pyridine was… 
1978
1978
Inhibition of monoamine oxidase by N-phenacyl-cyclopropylamine.
1963
1963
STRUCTURE AND ACTIVITY IN MOLLUSCICIDES: THE PHENACYL HALIDES, A GROUP OF POTENTIALLY USEFUL MOLLUSCICIDES.
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