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По вашему запросу найдено документов: 16

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Thioterpenoids as Potential Antithrombotic Drugs: Molecular Docking, Antiaggregant, Anticoagulant and Antioxidant Activities

Ksenofontov, Alexander A., Bocharov, Pavel S., Antina, Elena V., Shevchenko, Oksana G., Samorodov, Aleksandr V., Gilfanov, Ilmir R., Pavelyev, Roman S., Ostolopovskaya, Olga V., Startseva, Valeriya A., Fedyunina, Inna V., Azizova, Zulfiya R., Gaysin, Salavat I. (2022)

compounds on platelet aggregation was investigated by using the molecular docking technique. The obtained

MOLECULAR DOCKING AND PRECLINICAL STUDY OF FIVE-MEMBERED S,S-PALLADAHETEROCYCLE AS HEPATOPROTECTIVE AGENT

AKHMADIEV, N.S., AKHMETOVA, V.R., IBRAGIMOV, A.G., GALIMOVA, A.M., GALIMOVA, R.A., AGLETDINOV, E.F., KATAEV, V.A., KHAIRULLINA, V.R. (2019)

,S-palladaheterocycle, inhibition of cytochromes P450 has been modeled by molecular docking of four palladaheterocycle stereoisomers

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)

docking technique, we examined the effects of two series of “sulfide-sulfoxide-sulfone” thioterpenoids

NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA

D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S, Khusnutdinova, Elza K, Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)

topoisomerase I and II was studied. Resorting to the data of molecular docking, a probable mechanism

NOOTROPIC ACTIVITY OF A NOVEL (-)-CYTISINE DERIVATIVE (3AR,4S,8S,12R, 12AS,12BR)-10-METHYL-2-PHENYLOCTAHYDRO-1H-4,12A-ETHENO-8,12-METHANOPYRROLO[3’,4’:3,4]PYRIDO[1,2-A] [1,5]DIAZOCINE-1,3,5(4H)-TRIONE

Makara, N.S., Sapozhnikova, T.A., Khisamutdinova, R.Y., Tsypysheva, I.P., Borisevich, S.S., Kovalskaya, A.V., Petrova, P.R., Khursan, C.L., Zarudii, F.S. (2018)

functions of rats. According to molecular docking data, the nootropic activity of the compound can

NOVEL HYBRID MOLECULES ON THE BASIS OF STEROIDS AND (5Z,9Z)-TETRADECA-5,9-DIENOIC ACID: SYNTHESIS, ANTI-CANCER STUDIES AND HUMAN TOPOISOMERASE I INHIBITORY ACTIVITY

D’yakonov, V.A., Dzhemileva, L.U., Tuktarova, R.A., Ishmukhametova, S.R., Yunusbaeva, M.M., Ramazanov, I.R., Dzhemilev, U.M. (2017)

of in silico studies resorting to docking.

NZ,(N + 4)Z-DIENOIC FATTY ACIDS: A NEW METHOD FOR THE SYNTHESIS AND INHIBITORY ACTION ON TOPOISOMERASE I AND IIA

D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulyukova, Alfiya R., Baev, Dmitry S., Khusnutdinova, Elza K., Tolstikova, Tatiana G., Dzhemilev, Usein M. (2016)

topoisomerase I and II was studied. Resorting to the data of molecular docking, a probable mechanism

STEREOSELECTIVE SYNTHESIS OF 11-PHENYLUNDECA-5Z,9Z-DIENOIC ACID AND INVESTIGATION OF ITS HUMAN TOPOISOMERASE I AND IIA INHIBITORY ACTIVITY

Дьяконов, В.А., Джемилева, Л.У., Макаров, А.А., Мулюкова, А.Р., Хуснутдинова, Э.К., Джемилев, У.М., Baev, Dmitry S., Tolstikova, Tatiana G., D’yakonov, Vladimir A., Dzhemileva, Lilya U., Makarov, Aleksey A., Mulukova, Alfiya R., Khusnutdinova, Elza K., Dzhemilev, Usein M. (2015)

Molecular docking

11-PHENYLUNDECA-5Z,9Z-DIENOIC ACID: STEREOSELECTIVE SYNTHESIS AND DUAL TOPOISOMERASE I/IIΑ INHIBITION

Дьяконов, В.А., Джемилева, Л.У., Макаров, А.А., Мулюкова, А.Р., Хуснутдинова, Э.К., Джемилев, У.М., Толстикова Т. Г., Baev, D.S., D`yakonov, V.A., Dzhemileva, L.U., Makarov, A.A., Mulyukova, A.R., Khusnutdinova, E.K., Dzhemilev, U.M., Tolstikova, Tatiana G. (2015)

) was detected. Resorting to the data of molecular docking, a mechanism of inhibition was proposed.

EFFECTS OF NOVEL HEXAHYDROPYRIMIDINE DERIVATIVES AS POTENTIAL LIGANDS OF M1 MUSCARINIC ACETYLCHOLINE RECEPTOR ON COGNITIVE FUNCTION, HYPOXIA-INDUCED LETHALITY, AND OXIDATIVE STRESS IN RODENTS

SAPOZHNIKOVA, T.A., BORISEVICH, S.S., KIREEVA, D.R., GABDRAKHMANOVA, S.F., KHISAMUTDINOVA, R.Y., MAKARA, N.S., GIBADULLINA, N.N., KHURSAN, S.L., ZARUDII, F.S. (2019)

Molecular docking

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