Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vojtech Skopek"'
Autor:
Patrik Oleksak, Miroslav Psotka, Marketa Vancurova, Olena Sapega, Jana Bieblova, Milan Reinis, David Rysanek, Romana Mikyskova, Katarina Chalupova, David Malinak, Jana Svobodova, Rudolf Andrys, Helena Rehulkova, Vojtech Skopek, Pham Ngoc Lam, Jiri Bartek, Zdenek Hodny, Kamil Musilek
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 410-424 (2021)
Twelve novel analogs of STAT3 inhibitor BP-1-102 were designed and synthesised with the aim to modify hydrophobic fragments of the molecules that are important for interaction with the STAT3 SH2 domain. The cytotoxic activity of the reference and nov
Externí odkaz:
https://doaj.org/article/cfac0c0e4320428ab38cfae14e7c28f8
Autor:
Patrik, Oleksak, Miroslav, Psotka, Marketa, Vancurova, Olena, Sapega, Jana, Bieblova, Milan, Reinis, David, Rysanek, Romana, Mikyskova, Katarina, Chalupova, David, Malinak, Jana, Svobodova, Rudolf, Andrys, Helena, Rehulkova, Vojtech, Skopek, Pham, Ngoc Lam, Jiri, Bartek, Zdenek, Hodny, Kamil, Musilek
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Twelve novel analogs of STAT3 inhibitor BP-1-102 were designed and synthesised with the aim to modify hydrophobic fragments of the molecules that are important for interaction with the STAT3 SH2 domain. The cytotoxic activity of the reference and nov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::222100201d1b14a99eb79f6b9e1f39ad
https://pubmed.ncbi.nlm.nih.gov/33440995
https://pubmed.ncbi.nlm.nih.gov/33440995
Autor:
David Malinak, Pham Ngoc Lam, Marketa Vancurova, Romana Mikyšková, Vojtech Skopek, Kamil Musilek, Jana Svobodova, Helena Rehulkova, Zdenek Hodny, Miroslav Psotka, Milan Reinis, Olena Sapega, Jiri Bartek, Katarina Chalupova, Rudolf Andrys, David Rysanek, Patrik Oleksak, Jana Bieblová
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 410-424 (2021)
Twelve novel analogs of STAT3 inhibitor BP-1-102 were designed and synthesised with the aim to modify hydrophobic fragments of the molecules that are important for interaction with the STAT3 SH2 domain. The cytotoxic activity of the reference and nov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cac5c92173998608c522cc3e9dc3be
