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ChemMedChem ; 18(4): e202200526, 2023 02 14.
Article in English | MEDLINE | ID: mdl-36367256

ABSTRACT

Paracetamol and valproic acid are standalone drugs with leading position in the world drug market. The phosphonate analogues of these drugs were synthesized and were tested in vivo. N-(4-hydroxyphenylcarbamoyl)phosphonic acid was four times more potent than paracetamol in preventing acetic acid-induced writhing. Phosphonate derivative of valproic acid, (2-propylpentanoyl)phosphonic acid, had similar in vivo activity to valproic acid in the pentylenetetrazole-induced kindling mouse model.


Subject(s)
Organophosphonates , Valproic Acid , Mice , Animals , Valproic Acid/pharmacology , Acetaminophen/pharmacology , Organophosphonates/pharmacology , Phosphorous Acids/pharmacology
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