Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cleopatra Neagoie"'
Autor:
Sreenivas Avula, Xudan Peng, Xingfen Lang, Micky Tortorella, Béatrice Josselin, Stéphane Bach, Stephane Bourg, Pascal Bonnet, Frédéric Buron, Sandrine Ruchaud, Sylvain Routier, Cleopatra Neagoie
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 37, Iss 1, Pp 1632-1650 (2022)
A library of substituted indolo[2,3-c]quinolone-6-ones was developed as simplified Lamellarin isosters. Synthesis was achieved from indole after a four-step pathway sequence involving iodination, a Suzuki-Miyaura cross-coupling reaction, and a reduct
Externí odkaz:
https://doaj.org/article/eae579ca70af4ec7902f09b889e08fbc
Autor:
Alice Lanne, Yixin Cui, Edward Browne, Philip G. E. Craven, Nicholas J. Cundy, Nicholas J. Coltman, Katie Dale, Antonio Feula, Jon Frampton, Aaron Goff, Mariwan A. Hama Salih, Xingfen Lang, Xingjian Li, Christopher W. Moon, Michael Morton, Jordan Pascoe, Xudan Peng, Vanessa Portman, Cara Press, Timothy Schulz-Utermoehl, Micky Tortorella, Zhengchao Tu, Zoe E. Underwood, Changwei Wang, Akina Yoshizawa, Tianyu Zhang, Simon J Waddell, Joanna Bacon, Cleopatra Neagoie, John S. Fossey, Luke J. Alderwick.
Tuberculosis (TB) is the leading cause of global morbidity and mortality resulting from infectious disease, with over 10 million new cases and 1.5 million deaths in 2019. This global emergency is exacerbated by the emergence of multi-drug-resistant M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66e23350ab3888c21d9c850dce9078a6
https://doi.org/10.1101/2020.09.03.281170
https://doi.org/10.1101/2020.09.03.281170
Autor:
Frédéric Buron, Emeline Vedrenne, Cleopatra Neagoie, Olivier Lozach, Laurent Meijer, Stéphane Bourg, Sorin Rosca, Amélie Lansiaux, Sylvain Routier, Brigitte Baldeyrou, Jean-Yves Mérour
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-396. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-96. ⟨10.1016/j.ejmech.2012.01.040⟩
European Journal of Medicinal Chemistry, Elsevier, 2012, 49, pp.379-396. ⟨10.1016/j.ejmech.2012.01.040⟩
International audience; A library of substituted chromeno[3,4-b]indoles was developed as Lamellarin isosters. Synthesis was achieved from indoles after a four-step pathway sequence involving C-3 iodination, a Suzuki cross-coupling reaction, and a one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4320509b2a76082675976c07f0489bdb
https://doi.org/10.1016/j.ejmech.2012.01.040
https://doi.org/10.1016/j.ejmech.2012.01.040
Autor:
Youssef Hajbi, Berenger Biannic, Jean-Yves Mérour, Sorin Rosca, Aurelie Chilloux, Sylvain Routier, Brigitte Baldeyrou, Emeline Vedrenne, Cleopatra Neagoie, Amélie Lansiaux, Christian Bailly
Publikováno v:
European Journal of Medicinal Chemistry. 45:5428-5437
New 1,5-dihydro-4-(substituted phenyl)-3H-furo[3,4-b]carbazol-3-ones were synthesised via a key step Diels-Alder reaction under microwave irradiation. 3-Formylindole was successfully used in a 6-step synthesis to obtain those complex heterocycles. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cca711c6ce3daf052c874d1232ed0df9
https://doi.org/10.1016/j.ejmech.2010.09.003
https://doi.org/10.1016/j.ejmech.2010.09.003