Sintez sul`fonilamidov, soderzhashhix izoksazol`ny`j fragment
Author:
Affiliation:
1. Yaroslavl State Pedagogical University named after K.D. Ushinsky
Publisher
Yaroslavl State Technical University
Reference25 articles.
1. Chinthakindi P.K., Naicker T., Thota N., Govender T., Kruger H.G., Arvidsson P.I. Sulfonimidamides in Medicinal and Agricultural Chemistry // Angew. Chem. Int. Ed. 2017. Vol. 56. P. 4100–4109. DOI: 10.1002/anie.201610456., Chinthakindi P.K., Naicker T., Thota N., Govender T., Kruger H.G., Arvidsson P.I. Sulfonimidamides in Medicinal and Agricultural Chemistry // Angew. Chem. Int. Ed. 2017. Vol. 56. P. 4100–4109. DOI: 10.1002/anie.201610456.
2. Abd El-Karim S.S., Anwar M.M., Syam Y.M., Nael M.A., Ali H.F., Motaleb M.A. Rational design and synthesis of new tetralin-sulfonamide derivatives as potent anti-diabetics and DPP-4 inhibitors: 2D & 3D QSAR, in vivo radiolabeling and bio distribution studies // Bioorg. Chem. 2018. Vol. 81. P. 481–493. DOI: 10.1016/j.bioorg.2018.09.021., Abd El-Karim S.S., Anwar M.M., Syam Y.M., Nael M.A., Ali H.F., Motaleb M.A. Rational design and synthesis of new tetralin-sulfonamide derivatives as potent anti-diabetics and DPP-4 inhibitors: 2D & 3D QSAR, in vivo radiolabeling and bio distribution studies // Bioorg. Chem. 2018. Vol. 81. P. 481–493. DOI: 10.1016/j.bioorg.2018.09.021.
3. Said M.A., Eldehna W.M., Nocentini A., Fahim S.H., Bonardi A., Elgazar A.A., Kryštof V., Soliman D.H., Abdel-Aziz H.A., Gratteri P., Abou-Seri S.M., Supuran C.T. Sulfonamide-based ring-fused analogues for CAN508 as novel carbonic anhydrase inhibitors endowed with antitumor activity: Design, synthesis, and in vitro biological evaluation // Eur. J. Med. Chem. 2020. Vol. 189. 112019. DOI: 10.1016/j.ejmech.2019.112019., Said M.A., Eldehna W.M., Nocentini A., Fahim S.H., Bonardi A., Elgazar A.A., Kryštof V., Soliman D.H., Abdel-Aziz H.A., Gratteri P., Abou-Seri S.M., Supuran C.T. Sulfonamide-based ring-fused analogues for CAN508 as novel carbonic anhydrase inhibitors endowed with antitumor activity: Design, synthesis, and in vitro biological evaluation // Eur. J. Med. Chem. 2020. Vol. 189. 112019. DOI: 10.1016/j.ejmech.2019.112019.
4. Moskalik M.Y. Sulfonamides with Heterocyclic Periphery as Antiviral Agents // Molecules. 2023. Vol. 28, no. 1. P. 51. DOI: 10.3390/molecules28010051., Moskalik M.Y. Sulfonamides with Heterocyclic Periphery as Antiviral Agents // Molecules. 2023. Vol. 28, no. 1. P. 51. DOI: 10.3390/molecules28010051.
5. He F., Shi J., Wang Y., Wang S., Chen J., Gan X., Song B., Hu D. Synthesis, Antiviral Activity, and Mechanisms of Purine Nucleoside Derivatives Containing a Sulfonamide Moiety // J. Agric. Food Chem. 2019. Vol. 67. P. 8459–8467. DOI: 10.1021/acs.jafc.9b02681., He F., Shi J., Wang Y., Wang S., Chen J., Gan X., Song B., Hu D. Synthesis, Antiviral Activity, and Mechanisms of Purine Nucleoside Derivatives Containing a Sulfonamide Moiety // J. Agric. Food Chem. 2019. Vol. 67. P. 8459–8467. DOI: 10.1021/acs.jafc.9b02681.
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