Zobrazeno 1 - 10
of 96
pro vyhledávání: '"sceptrin"'
Autor:
Timothy F. Jamison, Long V. Nguyen
Publikováno v:
Organic Letters
A four-step synthesis of the dimeric pyrrole–imidazole alkaloid sceptrin is reported. The brevity of the route is based on a simple solution developed for selective assembly of the cyclobutane core of the natural product. The photochemical intermol
Autor:
Oh-Seok Kwon, Donghwa Kim, Heegyu Kim, Yeon-Ju Lee, Hyi-Seung Lee, Chung J. Sim, Dong-Chan Oh, Sang Kook Lee, Ki-Bong Oh, Jongheon Shin
Publikováno v:
Marine Drugs, Vol 16, Iss 12, p 513 (2018)
Two new sceptrin derivatives (1,2) and eight structurally-related known bromopyrrole-bearing alkaloids were isolated from the tropical sponge Agelas kosrae. By a combination of spectroscopic methods, the new compounds, designated dioxysceptrin (1) an
Externí odkaz:
https://doaj.org/article/c971386e0d814435addacb404a4c54e6
Publikováno v:
Molecules, Vol 6, Iss 2, Pp 130-141 (2001)
By specifically targeting sponges likely to contain oroidin derivatives, we have, for the first time, identified Australian sponges that contain sceptrin (2) and related compounds. Using a simple extraction technique and HPLC (with a photodiode array
Externí odkaz:
https://doaj.org/article/e853e7cd2ea94a50a3d04e13d38c64df
Autor:
Yaseen A.M.M. Elshaier, Ahmed Mostafa, Khaled A.M. Abouzid, Inas A. Abdallah, Hanan Elimam, Hend Mohamed Abdel-Bar, Marwa A. A. Fayed, Yassmin Moatasim, Mohammed Farrag El-Behairy
Publikováno v:
Arabian Journal of Chemistry, Vol 14, Iss 4, Pp 103092-(2021)
Arabian Journal of Chemistry
Arabian Journal of Chemistry
Graphical abstract
This work was a structured virtual screening for marine bioactive compounds with reported antiviral activities which were subjected to structure-based studies against SARS-CoV-2 co-crystallized proteins. The molecular docking
This work was a structured virtual screening for marine bioactive compounds with reported antiviral activities which were subjected to structure-based studies against SARS-CoV-2 co-crystallized proteins. The molecular docking
Akademický článek
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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:
Ludmila Ermolenko, Pascal Retailleau, Mathilde Corbin, Thanh Binh Nguyen, Ali Al-Mourabit, Le Anh Nguyen
Publikováno v:
European Journal of Organic Chemistry. 2018:5861-5868
Autor:
Jongheon Shin, Yeon-Ju Lee, Hyi-Seung Lee, Oh Seok Kwon, Sang Kook Lee, Heegyu Kim, Donghwa Kim, Ki-Bong Oh, Chung J. Sim, Dong-Chan Oh
Publikováno v:
Marine Drugs, Vol 16, Iss 12, p 513 (2018)
Marine Drugs
Volume 16
Issue 12
Marine Drugs
Volume 16
Issue 12
Two new sceptrin derivatives (1,2) and eight structurally-related known bromopyrrole-bearing alkaloids were isolated from the tropical sponge Agelas kosrae. By a combination of spectroscopic methods, the new compounds, designated dioxysceptrin (1) an
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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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