TANC, MUHAMMET
 Distribuzione geografica
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Continente #
NA - Nord America 2.754
EU - Europa 998
AS - Asia 228
AF - Africa 10
Continente sconosciuto - Info sul continente non disponibili 1
Totale 3.991
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Nazione #
US - Stati Uniti d'America 2.749
RU - Federazione Russa 359
PL - Polonia 272
IE - Irlanda 108
IT - Italia 97
SG - Singapore 75
CN - Cina 68
SE - Svezia 68
HK - Hong Kong 48
FI - Finlandia 37
ES - Italia 26
IN - India 25
GB - Regno Unito 11
CI - Costa d'Avorio 10
DE - Germania 9
CA - Canada 5
UA - Ucraina 5
JO - Giordania 4
RO - Romania 4
VN - Vietnam 4
KR - Corea 2
EU - Europa 1
JP - Giappone 1
LT - Lituania 1
NL - Olanda 1
TR - Turchia 1
Totale 3.991
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Città #
Fairfield 489
Santa Clara 377
Warsaw 272
Woodbridge 234
Seattle 230
Ashburn 215
Cambridge 193
Houston 162
Wilmington 162
Chandler 131
Dublin 108
Princeton 73
Ann Arbor 71
Altamura 69
Singapore 66
Lawrence 57
Boston 31
Barcelona 26
Hong Kong 23
Mumbai 20
Shanghai 19
Medford 16
San Diego 16
Beijing 15
Florence 14
Abidjan 10
Boardman 10
London 7
Detroit 6
New York 6
Norwalk 6
Siena 5
Dong Ket 4
Düsseldorf 4
Falls Church 4
Helsinki 4
Hillsboro 4
Laurel 4
Toronto 4
Andover 3
Gavirate 3
Yubileyny 3
Grevenbroich 2
Guangzhou 2
Hefei 2
Kent 2
Los Angeles 2
Moscow 2
Phoenix 2
Rome 2
Seoul 2
West Jordan 2
Acton 1
Arezzo 1
Buffalo 1
Böblingen 1
Cedar Knolls 1
Foshan 1
Izmir 1
Jinhua 1
Misano Adriatico 1
Munich 1
Prescot 1
Pune 1
Redmond 1
Redwood City 1
Rui'an 1
Shenzhen 1
Triggiano 1
Washington 1
Wuhan 1
Wuxi 1
Xuzhou 1
Zibo 1
Totale 3.218
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Nome #
Isatin-pyrazole benzenesulfonamide hybrids potently inhibit tumor-associated carbonic anhydrase isoforms IX and XII 216
Synthesis of novel acridine bis-sulfonamides with effective inhibitory activity against the carbonic anhydrase isoforms I, II, IX and XII 215
Deciphering the Mechanism of Human Carbonic Anhydrases Inhibition with Sulfocoumarins: Computational and Experimental Studies 149
6-Substituted 1,2-benzoxathiine-2,2-dioxides are isoform-selective inhibitors of human carbonic anhydrases IX, XII and VA. 131
3-Hydroxy-1H-quinazoline-2,4-dione as a New Scaffold to Develop Potent and Selective Inhibitors of the Tumor-Associated Carbonic Anhydrases IX and XII 127
6-substituted sulfocoumarins are selective carbonic anhdydrase IX and XII Inhibitors with significant cytotoxicity against colorectal cancer cells 124
Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol 123
Carbonic anhydrase inhibitors: Synthesis and inhibition of the human carbonic anhydrase isoforms I, II, IX and XII with benzene sulfonamides incorporating 4- and 3-nitrophthalimide moieties 118
9,10-Dibromo-N-aryl-9,10-dihydro-9,10-[3,4]epipyrroloanthracene-12,14-diones: Synthesis and Investigation of Their Effects on Carbonic Anhydrase Isozymes I, II, IX, and XII 117
6-Triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrases IX and XII 112
Exploring carbonic anhydrase inhibition with multimeric coumarins displayed on a fullerene scaffold 112
Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3- and 4-(hetero)arylisoxazol-5-amine scaffolds 111
Carbonic anhydrase inhibitors: Synthesis and inhibition of the human carbonic anhydrase isoforms I, II, VII, IX and XII with benzene sulfonamides incorporating 4,5,6,7-tetrabromophthalimide moiety 108
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 105
Isoform-selective inhibitory profile of 2-imidazoline-substituted benzene sulfonamides against a panel of human carbonic anhydrases 103
Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II 103
Synthesis and carbonic anhydrase inhibitory properties of amino acid – coumarin/quinolinone conjugates incorporating glycine, alanine and phenylalanine moieties 103
Synthesis and bioactivity studies of 1-aryl-3-(2-hydroxyethylthio)-1-propanones 102
Microwave assisted synthesis of novel tetrazole/sulfonamide derivatives based on octahydroacridine, xanthene and chromene skeletons as inhibitors of the carbonic anhydrases isoforms I, II, IV and VII 100
Synthesis of 6-tetrazolyl-substituted sulfocoumarins acting as highly potent and selective inhibitors of the tumor-associated carbonic anhydrase isoforms IX and XII 100
Fluorinated pyrrolidines and piperidines incorporating tertiary benzenesulfonamide moieties are selective carbonic anhydrase II inhibitors 99
The inhibitory effects of phenolic Mannich bases on carbonic anhydrase I and II isoenzymes 99
Carbonic anhydrase inhibitors: Synthesis and inhibition of the cytosolic mammalian carbonic anhydrase isoforms I, II and VII with benzene sulfonamides incorporating 4,5,6,7-tetrachlorophthalimide moiety 99
Synthesis and carbonic anhydrase isoenzymes I, II, IX, and XII inhibitory effects of dimethoxybromophenol derivatives incorporating cyclopropane moieties 98
A class of carbonic anhydrase I – selective activators 98
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 98
Synthesis, characterization and carbonic anhydrase inhibitory activity of novel benzothiazole derivatives 98
Synthesis of 6-aryl-substituted sulfocoumarins and investigation of their carbonic anhydrase inhibitory action 97
Synthesis and carbonic anhydrase inhibitory properties of sulfamides structurally related to dopamine 95
Synthesis and carbonic anhydrase I, II, IV and XII inhibitory properties of N-protected amino acid – sulfonamide conjugates 94
Microwave assisted synthesis of novel acridine–acetazolamide conjugates and investigation of their inhibition effects on human carbonic anhydrase isoforms hCA I, II, IV and VII 89
Dominant behaviours in the expression of human carbonic anhydrase hCA i activity 86
5-Aryl-1H-pyrazole-3-carboxylic acids as selective inhibitors of human carbonic anhydrases IX and XII 86
3-Hydroxy-1H-quinazoline-2,4-dione derivatives as new potent and selective inhibitors of the tumor-associated carbonic anhydrase IX and XII. 80
α-carbonic anhydrases possess thioesterase activity 78
Synthesis of novel acridine and bis acridine sulfonamides with effective inhibitory activity against the cytosolic carbonic anhydrase isoforms II and VII 71
CO2-capture by engineered mammalian carbonic anhydrases 54
Effective Access to Multivalent Inhibitors of Carbonic Anhydrases Promoted by Peptide Bioconjugation 41
Totale 4.039
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Categoria #
all - tutte 11.052
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.052
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020692 0 0 0 0 0 150 133 138 136 53 62 20
2020/2021381 33 42 17 56 18 20 15 37 44 61 29 9
2021/2022224 10 11 30 4 4 10 8 23 13 12 23 76
2022/2023593 99 165 45 24 25 90 59 21 48 4 10 3
2023/2024153 8 22 33 8 22 13 4 25 5 3 7 3
2024/2025982 51 178 65 197 489 2 0 0 0 0 0 0
Totale 4.039