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The inhibitory effects of phenolic Mannich bases on carbonic anhydrase I and II isoenzymes.Synthesis and bioactivities of halogen bearing phenolic chalcones and their corresponding bis Mannich bases.Synthesis, cytotoxicity and carbonic anhydrase inhibitory activities of new pyrazolines.Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1-propanones.Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3H-indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides.Synthesis of mono Mannich bases of 2-(4-hydroxybenzylidene)-2,3-dihydroinden-1-one and evaluation of their cytotoxicities.Synthesis of some acrylophenones with N-methylpiperazine and evaluation of their cytotoxicities.Synthesis of 3-aroyl-4-aryl-1-isopropylamino-4-piperidinols and evaluation of the cytotoxicities of the compounds against human hepatoma and breast cancer cell lines.Synthesis and biological evaluation of 1,5-bis(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one and its aminomethyl derivatives.1-(3-aminomethyl-4-hydroxyphenyl)-3-pyridinyl-2-propen-1-ones: a novel group of tumour-selective cytotoxins.3-Arylidene-1-(4-nitrophenylmethylene)-3,4-dihydro-1H-naphthalen-2-ones and related compounds displaying selective toxicity and reversal of multidrug resistance in neoplastic cells.Carbonic anhydrase inhibitors. Phenols incorporating 2- or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae β-carbonic anhydrase.Anti-inflammatory activity of 3-benzoyl-1-methyl-4-phenyl-4-piperidinol hydrochloride.Synthesis of 1-Aryl-3-phenethylamino-1-propanone hydrochlorides as possible potent cytotoxic agents.Synthesis, molecular modeling, and biological evaluation of 4-[5-aryl-3-(thiophen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes.New anticancer drug candidates sulfonamides as selective hCA IX or hCA XII inhibitors.Curcumin analogue 1,5-bis(4-hydroxy-3-((4-methylpiperazin-1-yl)methyl)phenyl)penta-1,4-dien-3-one mediates growth arrest and apoptosis by targeting the PI3K/AKT/mTOR and PKC-theta signaling pathways in human breast carcinoma cells.Synthesis of 4-(2-substituted hydrazinyl)benzenesulfonamides and their carbonic anhydrase inhibitory effects.Designing, synthesis and bioactivities of 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamides.Antifungal evaluation of bis Mannich bases derived from acetophenones and their corresponding piperidinols and stability studiesSynthesis and antifungal evaluation of 1-aryl-2-dimethyl- aminomethyl-2-propen-1-one hydrochloridesInhibitory effects of isatin Mannich bases on carbonic anhydrases, acetylcholinesterase, and butyrylcholinesteraseInhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and IISynthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolinesSynthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Halise Inci Gul
@ast
Halise Inci Gul
@en
Halise Inci Gul
@es
Halise Inci Gul
@nl
Halise Inci Gul
@sl
type
label
Halise Inci Gul
@ast
Halise Inci Gul
@en
Halise Inci Gul
@es
Halise Inci Gul
@nl
Halise Inci Gul
@sl
prefLabel
Halise Inci Gul
@ast
Halise Inci Gul
@en
Halise Inci Gul
@es
Halise Inci Gul
@nl
Halise Inci Gul
@sl
P108
P106
P1153
56248637500
6505465983
P31
P496
0000-0001-6164-9602