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Accueil > Recherche > Publications / brevets > Publications équipe SMALL > Synthèse valo biomolécules
X. P. He, C. Li, Z. Z. Wang, L. X. Gao, X. X. Shi, Y. Tang, J. Xie, J. Li, G. R. Chen and K. X. Chen Glycoconjugate J., 2011, 28, 7, 493-497
Glycoconjugate J., 2011, 28, 7, 493-497
X. P. He, C. Li, Z. Z. Wang, L. X. Gao, X. X. Shi, Y. Tang, J. Xie, J. Li, G. R. Chen and K. X. Chen
There has been increasing interest in the development of drug candidates based on sugar templates that possess rich structural and, especially, configurational diversities. We disclose herein that the epimeric identity between methyl 3,4-bis-phenylalanyl/tyrosinyl triazolyl-alpha-D-galactopyranoside and glucopyranoside may lead to their distinct inhibitory effects on specific protein tyrosine phosphatases (PTPs). Subsequently performed molecular docking study elucidated the plausible binding behaviors of the more potent galactosyl inhibitors with their primary PTP target, i.e. Cell Division Cycle 25B (CDC25B) phosphatase.
Le PPSM en couverture de Chemical Science
Clémence Allain lauréate de la médaille de bronze du CNRS 2017
Le Dr Clémence Allain lauréate de l'ERC starting grant 2016