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The antibiotic furagin and its derivatives are isoform-selective human carbonic anhydrase inhibitors
by
Pustenko, Aleksandrs
,
Nocentini, Alessio
,
Gratteri, Paola
,
Bonardi, Alessandro
,
Vozny, Igor
,
Žalubovskis, Raivis
,
Supuran, Claudiu T.
Published in
Journal of enzyme inhibition and medicinal chemistry
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Symmetric molecules with 1,4-triazole moieties as potent inhibitors of tumour-associated lactate dehydrogenase-A
by
Altamimi, Abdul-Malek S.
,
Alafeefy, Ahmed M.
,
Balode, Agnese
,
Vozny, Igor
,
Pustenko, Aleksandrs
,
El Shikh, Mohey Eldin
,
Alasmary, Fatmah A. S.
,
Abdel-Gawad, Sherif A.
,
Žalubovskis, Raivis
Published in
Journal of enzyme inhibition and medicinal chemistry
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5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: Solution and X-ray crystallographic studies
by
Leitans, Janis
,
Sprudza, Agnese
,
Tanc, Muhammet
,
Vozny, Igor
,
Zalubovskis, Raivis
,
Tars, Kaspars
,
Supuran, Claudiu T.
Published in
Bioorganic & medicinal chemistry
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Journal Of Enzyme Inhibition And Medicinal Chemistry
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Biochemistry & Molecular Biology
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Chemistry, Medicinal
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Humans
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Carbonic Anhydrase Inhibitors - Chemical Synthesis
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Backfile Package - Organic Chemistry (Legacy) [Yco]
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