Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Zhonghong Gan"'
Autor:
Hui Liu, Alireza Baradaran-Heravi, Keith Clinch, Jennifer M. Mason, Michel Roberge, Michael Popadynec, Olga V. Zubkova, Scott A. Cameron, Phillip M. Rendle, Dennis M. Whitfield, David A. Powell, Fengyang Yan, Benjamin Alford, Zhonghong Gan, Oscar Rebollo
Publikováno v:
ACS Med Chem Lett
[Image: see text] A significant proportion of genetic disease cases arise from truncation of proteins caused by premature termination codons. In eukaryotic cells some aminoglycosides cause readthrough of premature termination codons during protein tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aae307b2d261f09ba6a29e8c77cb102
https://europepmc.org/articles/PMC8436412/
https://europepmc.org/articles/PMC8436412/
Autor:
Zhonghong Gan, Prabhat Arya, P. Thirupathi Reddy, Nauzer Forbes, Donald M. Leek, S. Quevillon
Publikováno v:
Journal of Combinatorial Chemistry. 8:856-871
With the goal of developing a modular approach leading to different indoline alkaloid natural-product-like tricyclic derivatives having an unsaturated lactam (see compounds 13, 14, and 16), an aminoindoline-based bicyclic scaffold 10 was obtained fro
Autor:
Donald M. Leek, Prabhat Arya, S. Quevillon, M. Parisien, Patricia Durieux, D. Laforce, L.-C. Campeau, Reni Joseph, Z.‐X. Chen, Zhonghong Gan, S. Khadem, R. Kumar, Chang-Qing Wei, Malgosia Daroszewska, Michael L. Barnes, U. Sharma, E. Sesmilo, Samuel Couve-Bonnaire, P. T. Reddy
Publikováno v:
Pure and Applied Chemistry. 77:163-178
Due to the growing interest in small molecules that could help in understanding protein–protein interactions based on signal transduction, the demand for the generation of small-molecule libraries that are inspired by bioactive natural products has
Autor:
René Roy, Zhonghong Gan
Publikováno v:
Canadian Journal of Chemistry. 80:908-916
Clusters of O- and S-linked α-sialosides with valencies of two to four were constructed to serve as potential multivalent inhibitors towards sialoadhesins (siglecs). Thus, O- and S-prop-2-ynyl α-sialosides (3, 7), together with 4-iodophenyl sialosi
Autor:
René Roy, Zhonghong Gan
Publikováno v:
Tetrahedron. 56:1423-1428
Olefin metathesis catalyzed by RuCl2(CHPh)(PCy3)2 (1) has been used to synthesize homodimers of O- and S-alkenyl α-sialoside derivatives. The reactions afforded reasonable to good yields under mild reaction conditions. Trans-geometrical isomers were
Autor:
Zhonghong Gan, René Roy
Publikováno v:
Tetrahedron Letters. 41:1155-1158
Using copper(I)-catalyzed Glaser reaction and palladium-catalyzed Sonogashira reaction, divalent ‘rod-like’ thiomanno-, gluco, galacto, and lactoside clusters were prepared in high yields.
Publikováno v:
Carbohydrate Research. 318:75-81
Glycosylation of 4-nitrophenyl 2-acetamido-6-O-tert-butyldiphenylsilyl-2-deoxy-1-thio-beta-D-gluc opyranoside with phenyl 2,3,4,6-tetra-O-benzoyl-1-thio-beta-D-galactopyranoside in the presence of NIS and TfOH as catalyst gave the lactosamine derivat
Autor:
Lars T. Piehler, René Roy, Jon D. Reuter, Dujie Qin, Michael M. Hayes, Roseita Esfand, Donald A. Tomalia, Andrzej Myc, Rui Yin, Zhonghong Gan, James R. Baker
Publikováno v:
Bioconjugate Chemistry. 10:271-278
Multiple sialic acid (SA) residues conjugated to a linear polyacrylamide backbone are more effective than monomeric SA at inhibiting influenza-induced agglutination of red blood cells. However, "polymeric inhibitors" based on polyacrylamide backbones
Publikováno v:
Journal of Carbohydrate Chemistry. 18:755-773
An efficient methodology for regiospecific glycosylation was developed by using 6-O-tert-butyldiphenylsilyl N-acetylglucosamine derivatives 3 and 5 which bear two free hydroxyl groups as acceptors. The regiospecificity was attributed to the presence
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2005, 44 (9), pp.1366-1368. ⟨10.1002/anie.200462298⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2005, 44 (9), pp.1366-1368. ⟨10.1002/anie.200462298⟩
International audience; A library of tricyclic derivatives, similar to indoline alkaloids, has been generated by using a stereocontrolled, conjugate hetero‐Michael approach in both the solution and the solid phase (see scheme; P=protecting group, R