Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Biao Yu"'
Autor:
Fu, Jiqiang Please verify that the linked ORCID identifiers are correct for each author. The ORCID ID for 'Biao Yu' seems to be invalid. Please check and supply the correct ORCID ID. --> Please confirm that given names and surnames/family names have been iden1, Xu, Peng1,2 peterxu@sioc.ac.cn, Yu, Biao1,2 byu@sioc.ac.cn
Publikováno v:
Chinese Journal of Chemistry. Oct2021, Vol. 39 Issue 10, p2679-2684. 6p.
Publikováno v:
ACS Chemical Biology. 15:1016-1025
Aminoacyl-tRNA synthetases, the essential enzyme family for protein translation, are attractive targets for developing antibacterial, antifungal, and antiparasitic agents and for treating other human diseases. The antimalarial natural product cladosp
Publikováno v:
Natural Product Reports. 36:769-787
Covering: 1989–2017 Saponins are characteristic metabolites of starfish and sea cucumbers, and occasionally are also found in sponges, soft coral, and small fish. These steroid or triterpenoid glycosides often show remarkable biological and pharmac
Autor:
Biao Yu, Simone Nicolardi, Zhengnan Shen, Qian Zhu, Antonio Molinaro, Alba Silipo, Fabrizio Chiodo
Publikováno v:
Nature Communications
Nature Communications, 11(1). NATURE RESEARCH
Chiodo, F 2020, ' Chemical synthesis of glycans up to a 128-mer relevant to the O-antigen of Bacteroides vulgatus ', Nature Communications, vol. 11, no. 1, 4142 . https://doi.org/10.1038/s41467-020-17992-x
Nature Communications, Vol 11, Iss 1, Pp 1-7 (2020)
Nature Communications, 11(1):4142. Nature Publishing Group
Nature Communications, 11(1). NATURE RESEARCH
Chiodo, F 2020, ' Chemical synthesis of glycans up to a 128-mer relevant to the O-antigen of Bacteroides vulgatus ', Nature Communications, vol. 11, no. 1, 4142 . https://doi.org/10.1038/s41467-020-17992-x
Nature Communications, Vol 11, Iss 1, Pp 1-7 (2020)
Nature Communications, 11(1):4142. Nature Publishing Group
Glycans are involved in various life processes and represent critical targets of biomedical developments. Nevertheless, the accessibility to long glycans with precise structures remains challenging. Here we report on the synthesis of glycans consisti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25c637b0e482b6b09baef0df0782233c
https://hdl.handle.net/1887/3513377
https://hdl.handle.net/1887/3513377
Publikováno v:
The Journal of organic chemistry. 85(24)
Fucosylated chondroitin sulfates (FuCSs) are a unique type of polysaccharides occurring in sea cucumber that show a variety of biological activities. In particular, well-defined FuCS oligosaccharides, consisting of a trisaccharide repeating unit of
Publikováno v:
Chemical Reviews. 117:12281-12356
Advances in the chemical synthesis of C-pyranosides/furanosides are summarized, covering the literature from 2000 to 2016. The majority of the methods take advantage of the construction of the glycosidic C-C bond. These C-glycosylation methods are ca
Forsythenethoside A (1) is a structurally unique macrocyclic phenylethanoid glycoside, which was isolated from Forsynthia suspensa and displayed considerable neuroprotective activities. Here, we report its first chemical synthesis via a longest linea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e31a3c475ab28c25644a5a9d087b34c
http://hdl.handle.net/11588/767859
http://hdl.handle.net/11588/767859
Publikováno v:
BioFactors (Oxford, England). 42(5)
Mangiferin (2C-β-d-glucopyranosyl-1,3,6,7-tetrahydroxyxanthone) is a xanthone C-glycoside occurring in many plant species. Composed of a glucose unit C1→2 linked to a 1,3,6,7-tetrahydroxyxanthone aglycone, mangiferin exhibits a wide range of biolo
Publikováno v:
Tetrahedron Letters. 52:3075-3078
Glycosylation of the acid labile protopanaxadiol derivatives was succeeded with a glycosyl ortho -hexynylbenzoate as donor under the catalysis of PPh 3 AuNTf 2 , leading to the subsequent elaboration of ginsenoside Rh2 and chikusetsusaponin-LT8 in a
Publikováno v:
The Journal of Organic Chemistry. 74:5079-5082
Under the catalysis of DMAP or PPY in CH(2)Cl(2), the Michael-type addition of nucleophiles to 2-nitrogalactal or 2-nitroglucal leads in excellent yields and stereoselectivity to the corresponding beta-galacto- or -glucopyranosides, which are ready p