Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Ageliferin"'
Autor:
Heidi R. Bokesch, Kirk R. Gustafson, Emily A. Smith, Antony Wamiru, Dongdong Wang, Barry R. O'Keefe, Brice A P Wilson, Unwoo Kang, Wei Jiang, Ekaterina I. Goncharova, Donna Voeller, Stanley Lipkowitz
Publikováno v:
Marine Drugs
Volume 19
Issue 7
Marine Drugs, Vol 19, Iss 361, p 361 (2021)
Volume 19
Issue 7
Marine Drugs, Vol 19, Iss 361, p 361 (2021)
An extract of the coralline demosponge Astrosclera willeyana inhibited the ubiquitin ligase activity of the immunomodulatory protein Cbl-b. The bioassay-guided separation of the extract provided ten active compounds, including three new N-methyladeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbdd31d6e3b579ed1ef125b907c25945
Autor:
Juan C. Vázquez-Ucha, Jaime Rodríguez, Alejandro Beceiro, Marta Martínez-Guitián, Germán Bou, Cristina Lasarte-Monterrubio, Mar Pérez-Povedano, Carlos Jiménez, Dawrin Pech-Puch
Publikováno v:
RUC. Repositorio da Universidade da Coruña
Universitat Oberta de Catalunya (UOC)
Marine Drugs
Volume 18
Issue 6
Marine Drugs, Vol 18, Iss 326, p 326 (2020)
RUC: Repositorio da Universidade da Coruña
Universidade da Coruña (UDC)
Universitat Oberta de Catalunya (UOC)
Marine Drugs
Volume 18
Issue 6
Marine Drugs, Vol 18, Iss 326, p 326 (2020)
RUC: Repositorio da Universidade da Coruña
Universidade da Coruña (UDC)
The pyrrole-imidazoles, a group of alkaloids commonly found in marine sponges belonging to the genus Agelas, display a wide range of biological activities. Herein, we report the first chemical study of the secondary metabolites of the sponge A. dilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef261fcfc19d0fbb8fb1a5481e57d70
http://hdl.handle.net/2183/25903
http://hdl.handle.net/2183/25903
Autor:
Lena Barra, Jeroen S. Dickschat
Publikováno v:
European Journal of Organic Chemistry. 2017:4566-4571
The asymmetric synthesis of both enantiomers of tetrasubstituted all-trans dimethyl 3,4-diacetylcyclobutane-1,2-dicarboxylate with high enantiomeric purity (>98 % ee) using a valine-derived chiral auxiliary in a diastereoselective photodimerization i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b92ddb14678255daa08d4012e68ef8e3
https://doi.org/10.1002/ejoc.201700882
https://doi.org/10.1002/ejoc.201700882
Autor:
Frank Totzke, RuAngelie Edrada-Ebel, Mohamed S. Kamel, Roland Schmitz, Michael Kubbutat, Diaa T. A. Youssef, Werner E. G. Müller, Wim Wätjen, Peter Proksch, Mokhtar M. Bishr, Anja Bergermann, Ashraf Hamed
Fifteen pyrrole alkaloids were isolated from the Red Sea marine sponge Stylissa carteri and investigated for their biological activities. Four of them were dibrominated [(+) dibromophakelline, Z-3-bromohymenialdisine, (±) ageliferin and 3,4-dibromo-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4bc0dc344bc22373b6970322e5ff3c
https://strathprints.strath.ac.uk/64890/1/Hamed_etal_ZN_2018_Bioactive_pyrrole_alkaloids_isolated_from_the_Red_Sea.pdf
https://strathprints.strath.ac.uk/64890/1/Hamed_etal_ZN_2018_Bioactive_pyrrole_alkaloids_isolated_from_the_Red_Sea.pdf
Publikováno v:
Organic Chemistry Frontiers. 2:978-984
Sceptrins and nakamuric acid are structurally unique antibiotics isolated from marine sponges. Recent studies suggest that the biosynthesis of these dimeric pyrrole–imidazole alkaloids involves a single-electron transfer (SET)-promoted [2 + 2] cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49328485f2a1fad90a2edf63506719b0
https://doi.org/10.1039/c5qo00165j
https://doi.org/10.1039/c5qo00165j
Akademický článek
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Autor:
Thomas Lindel
More than a decade after our last review on the chemistry of the pyrrole-imidazole alkaloids, it was time to analyze once more the developments in that field. The comprehensive article focusses on the total syntheses of pyrrole-imidazole alkaloids th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c85ba228a81b41b1ae52e9b8935c493e
https://doi.org/10.1016/bs.alkal.2016.12.001
https://doi.org/10.1016/bs.alkal.2016.12.001
Autor:
Zhiqiang Ma, Shuanhu Gao, Arnold L. Rheingold, Curtis E. Moore, Xianghui Tan, Rodrigo A. Rodriguez, Chuo Chen, Xiao Wang, Yuyong Ma, Phil S. Baran, Xiaolei Wang
Publikováno v:
Science. 346:219-224
Cycloaddition is an essential tool in chemical synthesis. Instead of using light or heat as a driving force, marine sponges promote cycloaddition with a more versatile but poorly understood mechanism in producing pyrrole–imidazole alkaloids sceptri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2de0e593922c95e00fb778e636f9671
https://doi.org/10.1126/science.1255677
https://doi.org/10.1126/science.1255677
Publikováno v:
Tetrahedron Letters. 56:4502-4504
A new structurally unique bromopyrrole alkaloid, agelamadin F (1), comprising oroidin and 3-hydroxypyridinium was isolated from an Okinawan marine sponge Agelas sp. together with tauroacidin E (2), a new bromopyrrole alkaloid possessing a taurine moi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69fadc4c90073704fa7261ac287ca1ad
https://doi.org/10.1016/j.tetlet.2015.05.114
https://doi.org/10.1016/j.tetlet.2015.05.114
Publikováno v:
Chem. Sci.. 4:303-306
Ageliferin is a marine natural product having antiviral and antimicrobial activities. These functions remain to be characterized at a molecular level. Ageliferin is also thought a biosynthetic intermediary linking oroidin type alkaloids to more compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a2ab7a8f8eab44082fb2bc5b7b6009c
https://doi.org/10.1039/c2sc21651e
https://doi.org/10.1039/c2sc21651e