Search Results - "Salman, Aydın"
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Synthesis, antimycobacterial and antitumor activities of new (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl N,N-disubstituted dithiocarbamate/O-alkyldithiocarbonate derivatives
Published in Bioorganic & medicinal chemistry (01-12-2006)“…Reaction of 2-chloromethylsaccharin with substituted potassium dithiocarbamates and substituted potassium dithiocarbonates furnished…”
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Synthesis and biological evaluation of new 5-methyl-N-(3-oxo-1-thia-4-azaspiro[4.5]-dec-4-yl)-3-phenyl-1H-indole-2-carboxamide derivatives
Published in ARKIVOC (02-08-2006)Get full text
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N -(2,6-Dimethyl-3-oxo-1-thia-4-azaspiro[4.5]dec-4-yl)-2-hydroxy-2,2-diphenylacetamide
Published in Acta crystallographica. Section E, Structure reports online (01-10-2008)“…In the title compound, C24H28N2O3S, the pendant methyl C atom bonded to the cyclohexane ring is disordered over two sites in a 0.580 (11):0.420 (11) ratio. The…”
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Synthesis of new spiroindolinones incorporating a benzothiazole moiety as antioxidant agents
Published in European journal of medicinal chemistry (01-03-2010)“…3 H-Spiro[1,3-benzothiazole-2,3′-indol]-2′(1′ H)-ones 3a– c and 4a– e were synthesized from treating the 5-substituted 1 H-indole-2,3-diones with…”
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Discovery of Low Nanomolar and Subnanomolar Inhibitors of the Mycobacterial β-Carbonic Anhydrases Rv1284 and Rv3273
Published in Journal of medicinal chemistry (09-07-2009)“…A series of 2-(hydrazinocarbonyl)-3-aryl-1H-indole-5-sulfonamides has been derivatized by reaction with 2,4,6-trimethylpyrylium perchlorate, leading to…”
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Carbonic anhydrase inhibitors. Aromatic/heterocyclic sulfonamides incorporating phenacetyl, pyridylacetyl and thienylacetyl tails act as potent inhibitors of human mitochondrial isoforms VA and VB
Published in Bioorganic & medicinal chemistry (15-07-2009)“…K i (hCA I) = 263 nM, K i (hCA II) = 395 nM K i (hCA VA) = 7.1 nM, Ki (hCA VB) = 5.9 nM. A series of aromatic/heterocyclic sulfonamides incorporating…”
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Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors
Published in Bioorganic & medicinal chemistry letters (15-06-2009)“…K i (hCA I) = 108 nM, K i (hCA II) = 107 nM K i (hCA VII) = 4.7 nM. A series of aromatic/heterocyclic sulfonamides incorporating phenyl(alkyl),…”
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Synthesis and antituberculosis activity of 5-methyl/trifluoromethoxy-1 H-indole-2,3-dione 3-thiosemicarbazone derivatives
Published in Bioorganic & medicinal chemistry (2008)“…New series of 5-methyl/trifluoromethoxy-1 H-indole-2,3-dione 3-thiosemicarbazones 3a-t, 1-methyl-5-methyl/trifluoromethoxy-1 H-indole-2,3-dione…”
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Synthesis and biological evaluation of new 4-thiazolidinone derivatives
Published in Journal of enzyme inhibition and medicinal chemistry (01-08-2009)“…A series of new 2-aryl-4-thiazolidinones (3 and 4) was synthesized from 2-hydroxy-2,2-diphenyl-N'-[(substituted phenyl)methylene]acetohydrazides (2) and…”
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Carbonic anhydrase inhibitors. Synthesis of 2,4,6-trimethylpyridinium derivatives of 2-(hydrazinocarbonyl)-3-aryl-1H-indole-5-sulfonamides acting as potent inhibitors of the tumor-associated isoform IX and XII
Published in Bioorganic & medicinal chemistry letters (01-06-2009)“…KI (hCA I)=7.6nM; KI (hCA II)=65nM, KI (hCA IX)=8.3nM; KI (hCA XII)=9.5nM. A series of 2-(hydrazinocarbonyl)-3-aryl-1H-indole-5-sulfonamides possessing various…”
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Carbonic anhydrase inhibitors: Synthesis and inhibition studies against mammalian isoforms I–XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1 H-indole-5-sulfonamides
Published in Bioorganic & medicinal chemistry (2008)“…A series of 2-(hydrazinocarbonyl)-3-substitutedphenyl-1 H-indole-5-sulfonamides possessing various 2-, 3- or 4- substituted phenyl groups with methyl-,…”
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Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1 H-indole-5-sulfonamide with 12 mammalian isoforms: Kinetic and X-ray crystallographic studies
Published in Bioorganic & medicinal chemistry letters (2008)“…2-(Hydrazinocarbonyl)-3-phenyl-1 H-indole-5-sulfonamide was tested for its interaction with 12 carbonic anhydrase (CA, EC 4.2.1.1) isoforms in the search of…”
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Crystal Structure of (1,1-Dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl O-propyl dithiocarbonate
Published in Analytical Sciences ; X-ray Structure and Analysis Online (01-01-2008)“…The title compound, C12H13NO4S3, crystalizes in the monoclinic P1 space group. The unit-cell parameters of the title compound are a = 6.7172(6), b = 8.7344(8),…”
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Synthesis and antituberculosis activity of 5-methyl/trifluoromethoxy-1H-indole-2,3-dione 3-thiosemicarbazone derivatives
Published in Bioorganic & medicinal chemistry (01-10-2008)“…New series of 5-methyl/trifluoromethoxy-1H-indole-2,3-dione 3-thiosemicarbazones 3a-t, 1-methyl-5-methyl/trifluoromethoxy-1H-indole-2,3-dione…”
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Crystal structure of 1,1,3-trioxo-2,3-dihydro-1,2-benzisothiazol-2-ylmethyl 4-phenyl piperazine-1-carbodithioate, C 19 H 19 N 3 O 3 S 3
Published in Acta crystallographica. Section A, Foundations of crystallography (16-08-2009)“…Abstract only…”
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Crystal structure of 1,1,3-trioxo-2,3-dihydro-1,2-benzisothiazol-2-ylmethyl 4-phenyl piperazine-1-carbodithioate, C 19 H 19 N 3 O 3 S 3
Published in Acta crystallographica. Section A, Foundations of crystallography (16-08-2009)“…Abstract only…”
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Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms : Kinetic and X-ray crystallographic studies
Published in Bioorganic & medicinal chemistry (2008)“…2-(Hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide was tested for its interaction with 12 carbonic anhydrase (CA, EC 4.2.1.1) isoforms in the search of…”
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Spectrophotometric determination of drugs having primary amine group with p-dimethylaminocinnamaldehyde
Published in Turkish Journal of Pharmaceutical Sciences (2007)“…İki farklı tablet preparatındaki dapson ve metoklopramid HCl'in tayini için yeni bir metod verilmektedir. Reaksiyonlar oda sıcaklığında sırasıyla 9 ve 20…”
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