Výsledky vyhledávání - "E. Yashchenko"

Synthesis and cytotoxicity of methyl-substituted 8-quinolineselenolates of ruthenium, rhodium, osmium, and iridium

Autor: D. Zaruma, Edmunds Lukevics, Irina Shestakova, Ilona Domracheva, J. Ashaks, E. Yashchenko, V. Bridane

Publikováno v: Chemistry of Heterocyclic Compounds. 45:182-187

A series of 2-methyl, 4-methyl, and 2,4-dimethyl-8-quinolineselenolates of ruthenium, rhodium, osmium, and iridium has been synthesized and their cytotoxicity towards HT-1080 (human fibrosarcoma) and MG-22A (mouse hepatoma) tumor cells studied. It wa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c49b34f5d4db51c48590e3ce33ce2cc3
https://doi.org/10.1007/s10593-009-0248-0

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Synthesis of novel [1-aziridinyl-(hydroxyimino)methyl]arenes and their cytotoxic activity

Autor: A. Grigorjeva, Ivars Kalvinsh, V. Andrianov, Ilona Domracheva, Irina Shestakova, E. Yashchenko, Aigars Jirgensons

Publikováno v: Chemistry of Heterocyclic Compounds. 45:161-168

The synthesis has been developed for novel potential anticancer agents whose structures contain an aziridine amidoxime group. The cytotoxic activity of all of the target compounds on different cell lines are given together with the in vitro IC50 and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b16cbf7259f1fb5a462518a9fa59618f
https://doi.org/10.1007/s10593-009-0245-3

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Cytotoxic di(8-quinolyl) disulfides

Autor: J. Ashaks, Ilona Domracheva, D. Zaruma, Edmunds Lukevics, E. Yashchenko, Irina Shestakova

Publikováno v: Chemistry of Heterocyclic Compounds. 43:629-633

It has been shown that the nature of the substituent and its position in the quinoline ring markedly affects the antitumor activity and toxicity of di(8-quinolyl) disulfides. The greatest cytotoxicity in the series of methyl derivatives was shown by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::91459edba967e52464d96bd6611355f1
https://doi.org/10.1007/s10593-007-0097-7

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[Untitled]

Autor: Iveta Kanepe, E. Yashchenko, Edmunds Lukevics, K. I. Dikovskaya, Grigory Veinberg, Irina Shestakova, R. Bokaldere, Maksims Vorona

Publikováno v: Chemistry of Heterocyclic Compounds. 39:587-593

A series of 1,3,4-trisubstituted and 3,4-disubstituted 2-azetidinones were synthesized in order to study the relation between their structure and biological characteristics. Study of the cytotoxic activity of these compounds revealed an anticancer ef

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::31201d1789c7b624adbd23d81309a951
https://doi.org/10.1023/a:1025185830067

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Observation of the decay B0 ???K? (892)0

Autor: Sato, S., Yusa, Y., Mohanty, G.B., Abdesselam, A., Adachi, I., Aihara, H., Al Said, S., Asner, D.M., Aushev, T., Ayad, R., Bahinipati, S., Bakich, A.M., Bansal, V., Bhardwaj, V., Bhuyan, B., Bonvicini, G., Bozek, A., Bra?ko, M., Browder, T.E., ?ervenkov, D., Chang, P., Chekelian, V., Chen, A., Cheon, B.G., Chilikin, K., Cho, K., Chobanova, V., Choi, Y., Cinabro, D., Dalseno, J., Danilov, M., Dole�al, Z., Dr�sal, Z., Drutskoy, A., Eidelman, S., Farhat, H., Fast, J.E., Ferber, T., Frost, O., Gaur, V., Ganguly, S., Garmash, A., Gillard, R., Glattauer, R., Goh, Y.M., Golob, B., Grzymkowska, O., Hayasaka, K., Hayashii, H., He, X.H., Higuchi, T., Hou, W.-S., Huschle, M., Iijima, T., Inami, K., Ishikawa, A., Itoh, R., Iwasaki, Y., Jaegle, I., Joo, K.K., Julius, T., Kato, E., Kawasaki, T., Kim, D.Y., Kim, J.B., Kim, J.H., Kim, K.T., Kim, M.J., Kim, Y.J., Kinoshita, K., Klucar, J., Ko, B.R., Kody�, P., Korpar, S., Kri�an, P., Krokovny, P., Kuhr, T., Kumita, T., Kwon, Y.-J., Li, J., Li, Y., Libby, J., Liventsev, D., Matvienko, D., Miyabayashi, K., Miyata, H., Mizuk, R., Moll, A., Nakano, E., Nakao, M., Nanut, T., Natkaniec, Z., Nedelkovska, E., Nisar, N.K., Nishida, S., Ogawa, S., Okuno, S., Pakhlov, P., Pakhlova, G., Park, H., Pedlar, T.K., Petri?, M., Piilonen, L.E., Ritter, M., Rostomyan, A., Sakai, Y., Sandilya, S., Santelj, L., Sanuki, T., Sato, Y., Savinov, V., Schneider, O., Schnell, G., Schwanda, C., Schwartz, A.J., Semmler, D., Senyo, K., Seon, O., Sevior, M.E., Shebalin, V., Shen, C.P., Shibata, T.-A., Shiu, J.-G., Shwartz, B., Sibidanov, A., Simon, F., Sohn, Y.-S., Sokolov, A., Solovieva, E., Stari?, M., Steder, M., Stypula, J., Sumihama, M., Tamponi, U., Tatishvili, G., Teramoto, Y., Thorne, F., Trabelsi, K., Uchida, M., Uehara, S., Uglov, T., Unno, Y., Uno, S., Van Hulse, C., Vanhoefer, P., Varner, G., Vorobyev, V., Wagner, M.N., Wang, C.H., Wang, M.-Z., Wang, P., Wang, X.L., Watanabe, M., Watanabe, Y., Wehle, S., Williams, K.M., Won, E., Yashchenko, S., Yook, Y., Zhang, Z.P., Zhilich, V., Zhulanov, V., Zupanc, A.

Publikováno v: IndraStra Global.

We report a search for charmless hadronic decays of neutral B mesons to ??K?(892)0. The results are based on a 711fb-1 data sample that contains 772�106BB� pairs, collected at the (4S) resonance with the Belle detector at the KEKB asymmetric ener

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=issn23813652::1d046792bcb7617441286c342d3fc653
https://igi.indrastra.com/items/show/81825

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Synthesis and cytotoxicity of metal 4-methyl-8-quinolinethiolates

Autor: J. Ashaks, Edmunds Lukevics, I. Shestakova, Ilona Domracheva, D. Zaruma, E. Yashchenko

Publikováno v: Chemistry of Heterocyclic Compounds. 43:634-636

It has been shown that the introduction of a methyl group at position 4 of the quinoline ring in metal 8-quinolinethiolates brings about a significant increase in the selectivity of their cytotoxic activity. It was found that rhodium 4-methyl-8-quino

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f237d345b7bde1a1ff61f15e149d5135
https://doi.org/10.1007/s10593-007-0098-6

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