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Open Access publikációk letöltési adatai a DE intézményi repozitóriumából
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OA publikációk száma a DEA-ban: 25

Összes letöltés a DEA-ból: 2771

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United States (US)1671
China (CN)236
Hungary (HU)84
Russia (RU)75
France (FR)69
Germany (DE)59
India (IN)44
Ireland (IE)37
United Kingdom (GB)33
Netherlands (NL)31
Turkey (TR)26
Australia (AU)20
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Hong Kong S.A.R., China (HK)18
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n.a.152
Megjelenés Publication Fájlletöltések
2023Kacsir, I., Sipos, A., Kiss, T., Major, E., Bajusz, N., Tóth, E., Buglyó, P., Somsák, L., Kardos, G., Bai, P., Bokor, É.: Half sandwich-type osmium, ruthenium, iridium and rhodium complexes with bidentate glycosyl heterocyclic ligands induce cytostasis in platinum-resistant ovarian cancer cells and bacteriostasis in Gram-positive multiresistant bacteria.
Front. Chem. 11 1-18, 2023.
Folyóirat-mutatók:
Q1 Chemistry (miscellaneous) (2022)
kiadói változat: 54
2023Kacsir, I., Sipos, A., Major, E., Bajusz, N., Bényei, A., Buglyó, P., Somsák, L., Kardos, G., Bai, P., Bokor, É.: Half-sandwich type platinum-group metal complexes of C-Glucosaminyl azines: syntheses, antineoplastic and antimicrobial activities.
Molecules. 28 (7), 1-55, 2023.
Folyóirat-mutatók:
Q2 Analytical Chemistry (2022)
Q2 Chemistry (miscellaneous) (2022)
Q2 Drug Discovery (2022)
Q2 Medicine (miscellaneous) (2022)
Q3 Molecular Medicine (2022)
Q2 Organic Chemistry (2022)
Q1 Pharmaceutical Science (2022)
Q2 Physical and Theoretical Chemistry (2022)
kiadói változat: 15
2022Bokor, É., Ferenczi, A., Hashimov, M., Juhász-Tóth, É., Götz, Z., Zaki, A., Somsák, L.: First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions There of.
Molecules. 27 (22), 1-16, 2022.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q2 Chemistry (miscellaneous)
Q2 Drug Discovery
Q2 Medicine (miscellaneous)
Q3 Molecular Medicine
Q2 Organic Chemistry
Q1 Pharmaceutical Science
Q2 Physical and Theoretical Chemistry
kiadói változat: 3
2022Kacsir, I., Sipos, A., Bényei, A., Janka, E., Buglyó, P., Somsák, L., Bai, P., Bokor, É.: Reactive Oxygen Species Production Is Responsible for Antineoplastic Activity of Osmium, Ruthenium, Iridium and Rhodium Half-Sandwich Type Complexes with Bidentate Glycosyl Heterocyclic Ligands in Various Cancer Cell Models.
Int. J. Mol. Sci. 23 (2), 1-39, 2022.
Folyóirat-mutatók:
Q2 Catalysis
Q1 Computer Science Applications
D1 Inorganic Chemistry
Q1 Medicine (miscellaneous)
Q2 Molecular Biology
Q1 Organic Chemistry
Q1 Physical and Theoretical Chemistry
D1 Spectroscopy
kiadói változat: 56
2022Balázs, B., Tóth, Z., Kacsir, I., Sipos, A., Buglyó, P., Somsák, L., Bokor, É., Kardos, G., Bai, P.: Targeting multiresistant Gram-positive bacteria by ruthenium, osmium, iridium and rhodium half-sandwich type complexes with bidentate monosaccharide ligands.
Front. Chem. 10 1-9, 2022.
Folyóirat-mutatók:
Q1 Chemistry (miscellaneous)
kiadói változat: 14
2021Sipos, Á., Szennyes, E., Hajnal, É., Kun, S., Szabó, E., Uray, K., Somsák, L., Docsa, T., Bokor, É.: Dual-Target Compounds against Type 2 Diabetes Mellitus: proof of Concept for Sodium Dependent Glucose Transporter (SGLT) and Glycogen Phosphorylase (GP) Inhibitors.
Pharmaceuticals. 14 (4), 1-27, 2021.
Folyóirat-mutatók:
Q1 Drug Discovery
Q2 Molecular Medicine
Q1 Pharmaceutical Science
kiadói változat: 16
2021Kacsir, I., Sipos, A., Ujlaki, G., Buglyó, P., Somsák, L., Bai, P., Bokor, É.: Ruthenium half-sandwich type complexes with bidentate monosaccharide ligands show antineoplastic activity in ovarian cancer cell models through reactive oxygen species production.
Int. J. Mol. Sci. 221 1-41, 2021.
Folyóirat-mutatók:
Q2 Catalysis
Q1 Computer Science Applications
Q1 Inorganic Chemistry
Q1 Medicine (miscellaneous)
Q2 Molecular Biology
Q1 Organic Chemistry
Q1 Physical and Theoretical Chemistry
D1 Spectroscopy
kiadói változat: 62
2020Szennyes, E., Gyémánt, G., Somsák, L., Bokor, É.: Synthesis of New Series of 2-C-(béta-D-glucopyranosyl)-Pyrimidines and Their Evaluation as Inhibitors of Some Glycoenzymes.
Molecules. 25 (3), 1-18, 2020.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q1 Chemistry (miscellaneous)
Q2 Drug Discovery
Q2 Medicine (miscellaneous)
Q3 Molecular Medicine
Q2 Organic Chemistry
Q1 Pharmaceutical Science
Q2 Physical and Theoretical Chemistry
kiadói változat: 47
2019Somsák, L., Bokor, É., Juhász, L., Kun, S., Lázár, L., Juhász-Tóth, É., Tóth, M.: New syntheses towards C-glycosyl type glycomimetics.
Pure Appl. Chem. 91 (7), 1159-1175, 2019.
Folyóirat-mutatók:
Q2 Chemical Engineering (miscellaneous)
Q2 Chemistry (miscellaneous)
kiadói változat: 77
2018Nagy, L., Márton, J., Vida, A., Kis, G., Bokor, É., Kun, S., Gönczi, M., Docsa, T., Tóth, A., Antal, M., Gergely, P., Csóka, B., Pacher, P., Somsák, L., Bai, P.: Glycogen phosphorylase inhibition improves beta cell function.
Br. J. Pharmacol. 175 (2), 301-319, 2018.
Folyóirat-mutatók:
D1 Pharmacology
pre-print: 91
2018Kyriakis, E., Solovou, T., Kun, S., Czifrák, K., Szőcs, B., Juhász, L., Bokor, É., Stravodimos, G., Kantsadi, A., Chatzileontiadou, D., Skamnaki, V., Somsák, L., Leonidas, D.: Probing the [beta]-pocket of the active site of human liver glycogen phosphorylase with 3-(C-[beta]-D-glucopyranosyl)-5-(4-substituted-phenyl)-1, 2, 4-triazole inhibitors.
Bioorganic Chem. 77 485-493, 2018.
Folyóirat-mutatók:
Q3 Biochemistry
Q2 Drug Discovery
Q3 Molecular Biology
Q2 Organic Chemistry
pre-print: 155
2016Bokor, É., Széles, Z., Docsa, T., Gergely, P., Somsák, L.: C-Glucopyranosyl-1,2,4-triazol-5-ones: synthesis and inhibition of glycogen phosphorylase.
Carbohydr. Res. 429 128-134, 2016.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q3 Biochemistry
Q2 Medicine (miscellaneous)
Q2 Organic Chemistry
post-print: 128
2016Szennyes, E., Bokor, É., Batta, G., Docsa, T., Gergely, P., Somsák, L.: Improved preparation of 4(5)-aryl-2-(β-D-glucopyranosyl)-imidazoles, the most efficient glucose analogue inhibitors of glycogen phosphorylase.
RSC Adv. 6 (97), 94787-94794, 2016.
Folyóirat-mutatók:
Q1 Chemical Engineering (miscellaneous)
Q1 Chemistry (miscellaneous)
Kiadói változat: 135
2016Kantsadi, A., Bokor, É., Kun, S., Stravodimos, G., Chatzileontiadou, D., Leonidas, D., Juhász-Tóth, É., Szakács, A., Batta, G., Docsa, T., Gergely, P., Somsák, L.: Synthetic, enzyme kinetic, and protein crystallographic studies of C-[béta]-D-glucopyranosyl pyrroles and imidazoles reveal and explain low nanomolar inhibition of human liver glycogen phosphorylase.
Eur. J. Med. Chem. 123 737-745, 2016.
Folyóirat-mutatók:
Q1 Drug Discovery
Q1 Medicine (miscellaneous)
Q1 Organic Chemistry
Q1 Pharmacology
pre-print: 164
2015Bokor, É., Szennyes, E., Csupász, T., Tóth, N., Docsa, T., Gergely, P., Somsák, L.: C-(2-Deoxy-D-arabino-hex-1-enopyranosyl)-oxadiazoles: synthesis of possible isomers and their evaluation as glycogen phosphorylase inhibitors.
Carbohydr. Res. 412 71-79, 2015.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q3 Biochemistry
Q2 Medicine (miscellaneous)
Q2 Organic Chemistry
post-print: 138
2015Misra, A., Bokor, É., Kun, S., Bolyog-Nagy, E., Kathó, Á., Joó, F., Somsák, L.: Chemoselective hydration of glycosyl cyanides to C-glycosyl formamides using ruthenium complexes in aqueous media.
Tetrahedron Lett. 56 (44), 5995-5998, 2015.
Folyóirat-mutatók:
Q3 Biochemistry
Q2 Drug Discovery
Q2 Organic Chemistry
pre-print: 80
2015Szőcs, B., Bokor, É., Szabó, E., Kiss-Szikszai, A., Tóth, M., Somsák, L.: Synthesis of 5-aryl-3-C-glycosyl- and unsymmetrical 3,5-diaryl-1,2,4-triazoles from alkylidene-amidrazones.
RSC Advances. 5 (54), 43620-43629, 2015.
Folyóirat-mutatók:
Q1 Chemical Engineering (miscellaneous)
Q1 Chemistry (miscellaneous)
kiadói változat: 172
2014Kun, S., Bokor, É., Varga, G., Szőcs, B., Páhi, A., Czifrák, K., Tóth, M., Juhász, L., Docsa, T., Gergely, P., Somsák, L.: New synthesis of 3-(β-D-glucopyranosyl)-5-substituted-1,2,4- triazoles, nanomolar inhibitors of glycogen phosphorylase.
Eur. J. Med. Chem. 76 567-579, 2014.
Folyóirat-mutatók:
Q1 Drug Discovery
Q1 Medicine (miscellaneous)
Q1 Organic Chemistry
Q1 Pharmacology
post-print: 171
2014Somsák, L., Bokor, É., Czibere, B., Czifrák, K., Koppány, C., Kulcsár, L., Kun, S., Szilágyi, E., Tóth, M., Docsa, T., Gergely, P.: Synthesis of C-xylopyranosyl- and xylopyranosylidene-spiro-heterocycles as potential inhibitors of glycogen phosphorylase.
Carbohydr. Res. 399 38-48, 2014.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q3 Biochemistry
Q2 Medicine (miscellaneous)
Q2 Organic Chemistry
post-print: 205
2013Bokor, É., Fekete, A., Varga, G., Szőcs, B., Czifrák, K., Komáromi, I., Somsák, L.: C-(β-d-Glucopyranosyl)formamidrazones, formic acid hydrazides and their transformations into 3-(β-d-glucopyranosyl)-5-substituted-1,2,4-triazoles: a synthetic and computational study.
Tetrahedron. 69 (48), 10391-10404, 2013.
Folyóirat-mutatók:
Q2 Biochemistry
Q1 Drug Discovery
Q1 Organic Chemistry
post-print: 240
2013Bokor, É., Docsa, T., Gergely, P., Somsák, L.: C-Glucopyranosyl-1,2,4-triazoles As New Potent Inhibitors of Glycogen Phosphorylase.
ACS Med. Chem. Lett. 4 (7), 612-615, 2013.
Folyóirat-mutatók:
Q1 Biochemistry
D1 Drug Discovery
Q1 Organic Chemistry
post-print: 87
2013Bokor, É., Szilágyi, E., Docsa, T., Gergely, P., Somsák, L.: Synthesis of substituted 2-(β-d-glucopyranosyl)-benzimidazoles and their evaluation as inhibitors of glycogen phosphorylase.
Carbohydr. Res. 381C 179-186, 2013.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q3 Biochemistry
Q2 Medicine (miscellaneous)
Q2 Organic Chemistry
post-print: 156
2012Bokor, É., Koppány, C., Gonda, Z., Novák, Z., Somsák, L.: Evaluation of bis-triphenylphosphano-copper(I)-butyrate (C3H7COOCu(PPh3)2) as catalyst for the synthesis of 1-glycopyranosyl-4-substituted-1,2,3-triazoles.
Carbohydr. Res. 351 42-48, 2012.
Folyóirat-mutatók:
Q2 Analytical Chemistry
Q3 Biochemistry
Q2 Medicine (miscellaneous)
Q2 Organic Chemistry
post-print: 128
2010Cheng, K., Liu, J., Sun, H., Bokor, É., Czifrák, K., Kónya, B., Tóth, M., Docsa, T., Gergely, P., Somsák, L.: Tethered derivatives of D-glucose and pentacyclic triterpenes for homo/heterobivalent inhibition of glycogen phosphorylase.
New J. Chem. 34 1450-1464, 2010.
Folyóirat-mutatók:
Q2 Catalysis
Q1 Chemistry (miscellaneous)
Q1 Materials Chemistry
post-print: 117
2009Tóth, M., Kun, S., Bokor, É., Benltifa, M., Tallec, G., Vidal, S., Docsa, T., Gergely, P., Somsák, L., Praly, J.: Synthesis and structure-activity relationships of C-glycosylated oxadiazoles as inhibitors of glycogen phosphorylase.
Bioorg. Med. Chem. 17 (13), 4773-4785, 2009.
Folyóirat-mutatók:
Q2 Biochemistry
Q1 Clinical Biochemistry
Q1 Drug Discovery
Q3 Molecular Biology
Q2 Molecular Medicine
Q1 Organic Chemistry
Q1 Pharmaceutical Science
post-print: 260