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По вашему запросу найдено документов: 24

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Anticancer and Antiphytopathogenic Activity of Fluorinated Isatins and Their Water-Soluble Hydrazone Derivatives

Bogdanov, Andrei V., Neganova, Margarita, Voloshina, Alexandra, Lyubina, Anna, Amerhanova, Syumbelya, Litvinov, Igor A., Tsivileva, Olga, Akylbekov, Nurgali, Zhapparbergenov, Rakhmetulla, Valiullina, Zulfiia, Samorodov, Alexandr V., Alabugin, Igor (2023)

cells. In addition, compounds 3a and 3b exhibit platelet antiaggregation activity at the level

Design, synthesis, and bioactivity evaluation of novel 1-(4-(benzylsulfonyl)-2-nitrophenyl) derivatives as potential anti-inflammatory agents against LPS-induced ac

Chen, P., Yu, Y., Su, S., Du, Z., Cai, B., Sun, X., Chattipakorn, N., Samorodov, A.V., Pavlov, V.N., Tang, Q., Cho, W.-J., Liang, G. (2023)

in lipopolysaccharide (LPS)-challenged J774A.1 cells. Compounds 19, 20, and 39 potently reduced the release of IL-6

5-АМИНОЗАМЕЩЕННЫЕ ТИЕТАНСОДЕРЖАЩИЕ 3-БРОМ-4-НИТРОПИРАЗОЛЫ С АНТИДЕПРЕССИВНОЙ АКТИВНОСТЬЮ

5-AMINE-SUBSTITUTED THIETHANE-CONTAINING 3-BROMO-4-NITROPYRAZOLES WITH ANTIDEPRESSANT ACTIVITY

КЛЕН, Е.Э., НИКИТИНА, И.Л., ШЕПИЛОВА, С.О., НИКИТИНА, Е.А., ПАВЛОВ, В.Н., САМОРОДОВ, А.В., ХАЛИУЛЛИН, Ф.А., Klen, E.E., Nikitina, I.L., Shepilova, S.O., Nikitina, E.A., Pavlov, V.N., Samorodov, A.V., Khaliullin, F.A. (2023)

Unraveling the Mechanism of Platelet Aggregation Suppression by Thioterpenoids: Molecular Docking and In Vivo Antiaggregant Activity

Nikitina, Liliya E., Bocharov, Pavel S., Ksenofontov, Alexander A., Antina, Elena V., Gilfanov, Ilmir R., Pavelyev, Roman S., Ostolopovskaya, Olga V., Fedyunina, Inna V., Azizova, Zulfiya R., Pestova, Svetlana V., Izmest’ev, Evgeniy S., Rubtsova, Svetlana A., Boichuk, Sergei V., Galembikova, Aigul R., Smolyarchuk, Elena A., Mustafin, Ilshat G., Kayumov, Airat R., Samorodov, Aleksandr V. (2023)

for the design and production of novel biologically active compounds. In this study, by using the molecular

SYNTHESIS AND ANTIAGGREGANT AND ANTICOAGULANT ACTIVITY OF AMINO-ACID SALTS AND COMPUTER SIMULATION OF THE INTERACTION OF THEIR STRUCTURES WITH THE SURFACE OF CYCLOOXYGENASE

Gurevich, K.G., Urakov, A.L., Purygin, P.P., Abzalilov, T.A., Garaev, T.M., Zarubin, Y.P., Afanasiev, V.A., Sakaev, V.E., Samoredov, A.V., Pavlov, V.N., Lovtsova, L.V. (2023)

. It was hypothesized that compounds synthesized from natural amino acids would possess these pharmacological activities

Synthesis and Antidepressant Activity of Thietane-Containing 4-(2-oxo-2-phenylethyl)-1H-1,2,4-triazol-4-ium Bromides

Khaliullin, F.A., Klen, E.E., Nikitina, I.L., Pavlov, V.N., Rozit, G.A., Gaisina, G.G., Samorodov, A.V. (2023)

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy

Synthesis and Antidepressant Activity of Thietane-Containing 4-(2-oxo-2-phenylethyl)-1H-1,2,4-triazol-4-ium Bromides

Khaliullin, F. A., Klen, E. E., Nikitina, I. L., Pavlov, V. N., Rozit, G. A., Gaisina, G. G., Samorodov, A. V. (2023)

. The structures of the synthesized compounds were confirmed by IR, PMR, and 13C and 15N NMR spectroscopy

Thermal and electrical properties of nanocrystalline superionic NaxCu1.75S (x=0.1, 0.15, 0.2, 25) compounds

Kubenova, M.M., Kuterbekov, K.A., Balapanov, M.Kh., Ishembetov, R.Kh., Akhmetgaliev, B.M., Kabyshev, A.M., Bekmyrza, K.Zh., Zeleev, M.Kh., Palymbetov, R.Sh., Baikhozhaeva, B.U. (2023)

) compounds

Novel O-benzylcinnamic acid derivative L26 treats acute lung injury in mice by MD-2

Li, Xiang, Yin, Lina, Liao, Jing, Yang, Jun, Cai, Binhao, Yu, Yiming, Su, Sijia, Du, Zhiteng, Li, Xiaobo, Zhou, Ying, Chen, Pan, Cho, Won-Jea, Chattipakorn, Nipon, Samorodov, Aleksandr V., Pavlov, Valentin N., Zhang, Fengzhi, Liang, Guang, Tang, Qidong (2023)

and synthesized using cinnamic acid as the lead compound. We tested the preliminary anti-inflammatory activity

Cytotoxic Activity of A-Modified Licorice Triterpenoid Derivatives

Baltina, L. A., Khusnutdinova, N. S., Karimova, E. R., Saifullina, D. R., Kondratenko, R. M. (2023)

-7 breast adenocarcinoma, and SH-SY5Y neuroblastoma cells was studied. The most active compound

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