Search Results - "KARALI, Nilgün"
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Discovery of novel isatin-based sulfonamides with potent and selective inhibition of the tumor-associated carbonic anhydrase isoforms IX and XII
Published in Organic & biomolecular chemistry (21-06-2015)“…A series of 2/3/4-[(2-oxo-1,2-dihydro-3H-indol-3-ylidene)amino]benzenesulfonamides, obtained from substituted isatins and 2-, 3- or 4-aminobenzenesulfonamide,…”
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Histone deacetylase inhibitors providing an epigenetic treatment in cancer
Published in Istanbul journal of pharmacy (01-08-2021)“…Cancer is among the leading causes of death worldwide and is therefore one of the diseases in which there have been major medical advances and which is the…”
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Synthesis and structure-antituberculosis activity relationship of 1H-indole-2,3-dione derivatives
Published in Bioorganic & medicinal chemistry (01-09-2007)“…New series of 5-fluoro-1H-indole-2,3-dione-3-thiosemicarbazones 2a-k and 5-fluoro-1-morpholino/piperidinomethyl-1H-indole-2,3-dione-3-thiosemicarbazones 3a-r…”
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Synthesis, molecular modeling and antiviral activity of novel 5-fluoro-1H-indole-2,3-dione 3-thiosemicarbazones
Published in Bioorganic chemistry (01-11-2020)“…[Display omitted] •26 new 1-alkylated 5-fluoroisatin 3-thiosemicarbazone derivatives were synthesized.•Some derivatives were found effective against herpes…”
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Synthesis and primary antiviral activity evaluation of 3-hydrazono-5-nitro-2-indolinone derivatives
Published in ARKIVOC (05-11-2005)Get full text
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Antiviral activity and molecular modeling studies on 1H-indole-2,3-diones carrying a naphthalene moiety
Published in Journal of molecular structure (05-06-2023)“…•1H-indole-2,3-diones (2a-f) bearing a naphthalene ring were synthesized.•The antiviral effects of 2a-f were evaluated against different DNA and RNA…”
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Bioisosterism: 1,2,4‐Oxadiazole Rings
Published in ChemMedChem (02-05-2023)“…Although studies in drug discovery have gained momentum in recent years, the conversion of drugs in use today into less toxic derivatives with…”
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Novel sulfonamide-containing 2-indolinones that selectively inhibit tumor-associated alpha carbonic anhydrases
Published in Bioorganic & medicinal chemistry (15-07-2017)“…[Display omitted] Human carbonic anhydrases IX and XII are upregulated in many tumors and form a novel target for new generation anticancer drugs. Here we…”
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Synthesis and molecular modeling studies of 1-benzyl-2-indolinones as selective AChE inhibitors
Published in Future medicinal chemistry (01-12-2022)“…Possible bioisosteres can be developed by replacing the 1-indanone ring (one of three pharmacophore groups) of donepezil with an indoline ring. As H S donors,…”
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New 1H‐indole‐2,3‐dione 3‐thiosemicarbazones with 3‐sulfamoylphenyl moiety as selective carbonic anhydrase inhibitors
Published in Archiv der Pharmazie (Weinheim) (01-08-2022)“…1‐Methyl/ethyl/benzyl‐5‐(un)substituted 1H‐indole‐2,3‐diones (2, 3, and 4) were synthesized by reaction of 5‐(un)substituted 1H‐indole‐2,3‐diones (1) with…”
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Isatin analogs as novel inhibitors of Candida spp. β-carbonic anhydrase enzymes
Published in Bioorganic & medicinal chemistry (15-04-2016)“…[Display omitted] Enzyme inhibition data of structurally novel isatin-containing sulfonamides were determined for two carbonic anhydrases (CAs, EC 4.2.1.1)…”
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Anti-proliferative effects of indomethacin, acemetacin and their tromethamine salts in HCT116 human colon cancer cells
Published in Istanbul journal of pharmacy (01-08-2021)“…Background and Aims: Since 1980's, several preclinical studies have been published on the anti-colorectal cancer activity of the nonsteroidal anti-inflammatory…”
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5‐Fluoro/(trifluoromethoxy)‐2‐indolinone derivatives with anti‐interleukin‐1 activity
Published in Archiv der Pharmazie (Weinheim) (01-12-2023)“…The pro‐inflammatory cytokine interleukin‐1 (IL‐1) drives the pathogenesis of several inflammatory diseases. Recent studies have revealed that 2‐indolinones…”
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Synthesis, molecular modeling and cholinesterase inhibitory effects of 2-indolinone-based hydrazinecarbothioamides
Published in Future medicinal chemistry (01-12-2021)“…2-Indolinone-based hydrazinecarbothioamides carrying a 3-phenylsulfonamide moiety ( ) were designed by replacement of donepezil's pharmacophore group indanone…”
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Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme
Published in Journal of enzyme inhibition and medicinal chemistry (01-01-2019)“…Inhibition of the β-carbonic anhydrase (CA, EC 4.2.1.1) from pathogenic Candida glabrata (CgNce103) by 1H-indole-2,3-dione…”
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Molecular and crystal structure of 1-methyl- 5-trifluoromethoxy-1H-indole-2,3-dione 3-[4-(4-methoxyphenyl)thiosemicarbazone]
Published in Istanbul journal of pharmacy (01-04-2021)“…Background and Aims: The main purpose of this study is to determine the molecular structure and isomers of the new 1-methyl-…”
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Anticancer and antituberculosis effects of 5-fluoro- 1H-indole-2,3-dione 3-thiosemicarbazones
Published in Istanbul journal of pharmacy (01-12-2020)“…Background and Aims: The aim of this study was to screen the in vitro anticancer/antituberculosis activities of 5-fluoro- 1-methyl/ethyl-1H-indole-2,3-dione…”
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Three novel compounds of 5-trifluoromethoxy-1H-indole-2,3-dione 3-thiosemicarbazone: Synthesis, crystal structures and molecular interactions
Published in Journal of molecular structure (08-10-2013)“…•5-trifluoromethoxy-1H-indole-2,3-dione 3-thiosemicarbazone derivatives were synthesized.•The structures were determined by analytical, spectral and single XRD…”
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Selective Cytotoxic Effects of 5-Trifluoromethoxy-1H-indole-2,3-dione 3-Thiosemicarbazone Derivatives on Lymphoid-originated Cells
Published in Anti-cancer agents in medicinal chemistry (2022)“…The present study aims to identify the anticancer effect of novel 1H-indole-2,3-dione 3- thiosemicarbazone derivatives. These compounds could be promising…”
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Anticancer activities and cell death mechanisms of 1H-indole-2,3-dione 3-[N-(4 sulfamoylphenyl)thiosemicarbazone] derivatives
Published in Istanbul journal of pharmacy (01-12-2018)“…In this study, the cytotoxic effects of 1H-indole-2,3-dione 3-[N-(4-sulfamoylphenyl)thiosemicarbazone derivatives namely, 4a-d were evaluated using cell…”
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