Tudóstér: Szennyes Eszter publikációi

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feltöltött közlemény: 11 Open Access: 4
2023
  1. Bokor, É., Kecskés, D., Gombás, F., Fehér, A., Kardos, E., Dabian, A., Vonza, Z., Szennyes, E., Somsák, L.: First representatives of C-glycosyl 1,2,4,5-tetrazines: synthesis of 3-beta-d-glucopyranosyl 1,2,4,5-tetrazines and their transformation into 3-beta-d-glucopyranosyl pyridazines.
    New Journal of Chemistry 47 (1), 56-74, 2023.
    Folyóirat-mutatók:
    Q3 Catalysis (2022)
    Q2 Chemistry (miscellaneous) (2022)
    Q2 Materials Chemistry (2022)
2021
  1. Sipos, 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
2020
  1. Szennyes, 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
  2. Kyriakis, E., Karra, A., Papaioannou, O., Solovou, T., Skamnaki, V., Liggri, P., Zographos, S., Szennyes, E., Bokor, É., Kun, S., Psarra, A., Somsák, L., Leonidas, D.: The architecture of hydrogen and sulfur α-hole interactions explain differences in the inhibitory potency of C-β-d-glucopyranosyl thiazoles, imidazoles and an N-β-d glucopyranosyl tetrazole for human liver glycogen phosphorylase and offer new insights to structure-based design.
    Bioorg. Med. Chem. 28 (1), 1-10, 2020.
    Folyóirat-mutatók:
    Q3 Biochemistry
    Q2 Clinical Biochemistry
    Q2 Drug Discovery
    Q3 Molecular Biology
    Q3 Molecular Medicine
    Q2 Organic Chemistry
    Q2 Pharmaceutical Science
2019
  1. Barr, D., Szennyes, E., Bokor, É., Al-Oanzi, Z., Moffatt, C., Kun, S., Docsa, T., Sipos, Á., Davies, M., Mathomes, R., Snape, T., Agius, L., Somsák, L., Hayes, J.: Identification of C-[béta]-d-Glucopyranosyl Azole-Type Inhibitors of Glycogen Phosphorylase That Reduce Glycogenolysis in Hepatocytes: in Silico Design, Synthesis, in Vitro Kinetics, and ex Vivo Studies.
    ACS Chem. Biol. 14 (7), 1460-1470, 2019.
    Folyóirat-mutatók:
    Q1 Biochemistry
    D1 Medicine (miscellaneous)
    Q1 Molecular Medicine
  2. Szennyes, E., Bokor, É., Docsa, T., Sipos, Á., Somsák, L.: Synthesis of C-β-D-glucopyranosyl derivatives of some fused azoles for the inhibition of glycogen phosphorylase.
    Carbohydr. Res. 472 33-41, 2019.
    Folyóirat-mutatók:
    Q2 Analytical Chemistry
    Q3 Biochemistry
    Q2 Medicine (miscellaneous)
    Q2 Organic Chemistry
2018
  1. Kun, S., Begum, J., Kyriakis, E., Stamati, E., Barkas, T., Szennyes, E., Bokor, É., Szabó, E., Stravodimos, G., Sipos, Á., Docsa, T., Gergely, P., Moffatt, C., Patraskaki, M., Kokolaki, M., Gkerdi, A., Skamnaki, V., Leonidas, D., Somsák, L., Hayes, J.: A multidisciplinary study of 3-(β-D-glucopyranosyl)-5-substituted-1,2,4-triazole derivatives as glycogen phosphorylase inhibitors: computation, synthesis, crystallography and kinetics reveal new potent inhibitors.
    Eur. J. Med. Chem. 147 266-278, 2018.
    Folyóirat-mutatók:
    Q1 Drug Discovery
    Q1 Medicine (miscellaneous)
    Q1 Organic Chemistry
    Q1 Pharmacology
  2. Szennyes, E., Bokor, É., Langer, P., Gyémánt, G., Docsa, T., Sipos, Á., Somsák, L.: The first general synthesis of 2-C-(beta-D-glycopyranosyl)pyrimidines and their evaluation as inhibitors of some glycoenzymes.
    New J. Chem. 42 (21), 17439-17446, 2018.
    Folyóirat-mutatók:
    Q3 Catalysis
    Q2 Chemistry (miscellaneous)
    Q1 Materials Chemistry
2017
  1. Szennyes, E., Bokor, É., Kiss-Szikszai, A., Somsák, L., Pascal, Y.: Preparation of 2,6-anhydro-3,4,5,7-tetra-O-benzyl-D-glycero-D-gulo-heptonimidamide.
    In: Carbohydrate Chemistry: Proven Synthetic Methods / Christian Vogel, Paul Murphy, CRC Press-Taylor & Francis Group, Boca Raton, 323-332, 2017, (Volume 4 ) ISBN: 9781498726917
2016
  1. Szennyes, 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)
2015
  1. Bokor, 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
feltöltött közlemény: 11 Open Access: 4
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