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Inhibition of estrone sulfatase (ES) by alkyl and cycloalkyl ester derivatives of 4-[(aminosulfonyl)oxy] benzoic acid.

Kingston University

The mechanism of the irreversible inhibition of estrone sulfatase (ES) through the consideration of a range of methane- and amino-sulfonate-based compounds.

Kingston University

Inhibition of estrone sulfatase (ES) by derivatives of 4-[(aminosulfonyl)oxy] benzoic acid.

Kingston University

Design, synthesis and biochemical evaluation of AC ring mimics as novel inhibitors of the enzyme estrone sulfatase (ES).

Kingston University

Acid dissociation constant, a potential physicochemical factor in the inhibition of the enzyme estrone sulfatase (ES).

Kingston University

Novel inhibitors of the enzyme estrone sulfatase (ES).

Kingston University

Determination and use of a transition state for the enzyme estrone sulfatase (ES) from a proposed reaction mechanism.

Kingston University

Hydrophobicity, a physicochemical factor in the inhibition of the enzyme estrone sulfatase (ES).

Kingston University

Derivation of a possible transition-state for the reaction catalysed by the enzyme estrone Sulfatase (ES).

Kingston University

Structure activity relationship study of known inhibitors of the enzyme 5 alpha-reductase (5AR).

Kingston University

Synthesis, biochemical evaluation and rationalisation of the inhibitory activity of a range of 4-substituted phenyl alkyl imidazole-based inhibitors of the enzyme complex 17alpha-hydroxylase/17,20-lyase (P450(17alpha)).

Kingston University

Synthesis, biochemical evaluation and rationalisation of the inhibitory activity of a series of 4-hydroxyphenyl ketones as potential inhibitors of 17beta-hydroxysteroid dehydrogenase type 3 (17beta-HSD3).

Kingston University

Enzyme inhibition as a potential therapeutic strategy to treat COVID-19 infection.

Kingston University

Synthesis and biochemical evaluation of a range of potent benzyl imidazole-based compounds as potential inhibitors of the enzyme complex 17alpha-hydroxylase/17,20-lyase (P450(17alpha)).

Kingston University