30 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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23
Synthesis and carbonic anhydrase isoenzymes I, II, IX, and XII inhibitory effects of dimethoxybromophenol derivatives incorporating cyclopropane moieties.

Ataturk University
23
Synthesis of donepezil-based multifunctional agents for the treatment of Alzheimer's disease.

Ataturk University
11
N-Acylsulfonamides strongly inhibit human carbonic anhydrase isoenzymes I and II.

Ataturk University
9
Novel sulfamides as potential carbonic anhydrase isoenzymes inhibitors.

Ataturk University
16
Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols and their derivatives including natural products: vidalol B.

Ataturk University
12
In vitro inhibition of human erythrocyte glutathione reductase by some new organic nitrates.

Ataturk University
5
A novel and one-pot synthesis of new 1-tosyl pyrrol-2-one derivatives and analysis of carbonic anhydrase inhibitory potencies.

Ataturk University
12
NO-releasing esters show carbonic anhydrase inhibitory action against human isoforms I and II.

Ataturk University
11
Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols.

Ataturk University
10
In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II.

Ataturk University
24
Comprehensive study on potent and selective carbonic anhydrase inhibitors: Synthesis, bioactivities and molecular modelling studies of 4-(3-(2-arylidenehydrazine-1-carbonyl)-5-(thiophen-2-yl)-1H-pyrazole-1-yl) benzenesulfonamides.

Ataturk University
1
Design, synthesis and biological evaluation of 3,5-diaryl isoxazole derivatives as potential anticancer agents.

Ataturk University
8
Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine.

Ataturk University
14
Carbonic anhydrase inhibitors. Phenols incorporating 2- or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae -carbonic anhydrase.

Ataturk University
7
Synthesis and carbonic anhydrase isoenzymes I and II inhibitory effects of novel benzylamine derivatives.

Ataturk University
6
Carbonic anhydrase inhibitory properties of novel sulfonamide derivatives of aminoindanes and aminotetralins.

Ataturk University
7
Synthesis and paroxonase activities of novel bromophenols.

Ataturk University
5
Impacts of some antibiotics on human serum paraoxonase 1 activity.

Ataturk University
5
(3,4-Dihydroxyphenyl)(2,3,4-trihydroxyphenyl)methanone and its derivatives as carbonic anhydrase isoenzymes inhibitors.

Ataturk University
17
Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms I and II.

Ataturk University
15
Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI.

Ataturk University
4
In vitro effects of some drugs on human erythrocyte glutathione reductase.

Ataturk University
12
Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols including natural products.

Ataturk University
11
Effects of some drugs on human erythrocyte glucose 6-phosphate dehydrogenase: an in vitro study.

Ataturk University
7
Effects of some drugs on human erythrocyte 6-phosphogluconate dehydrogenase: an in vitro study.

Ataturk University
17
Synthesis of 4-[2-(3,4-dimethoxybenzyl)cyclopentyl]-1,2-dimethoxybenzene Derivatives and Evaluations of Their Carbonic Anhydrase Isoenzymes Inhibitory Effects.

Ataturk University
13
Antioxidant and acetylcholinesterase inhibition properties of novel bromophenol derivatives.

Ataturk University
6
Effect of some analgesics on paraoxonase-1 purified from human serum.

Ataturk University
6
An alternative purification method for human serum paraoxonase 1 and its interactions with sulfonamides.

Ataturk University
8
Carbonic anhydrase inhibitors: Inhibition of human erythrocyte isozymes I and II with a series of phenolic acids.

Ataturk University