Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gillian F. Whyte"'
Autor:
Agostino Cilibrizzi, Ramon Vilar, Marina Fedorova, Inna Guterman, Lok Hang Mak, Gillian F. Whyte, Rudiger Woscholski, Robin J. Leatherbarrow, Juliet Collins
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(16)
Vanadium complexes have been previously utilised as potent inhibitors of cysteine based phosphatases (CBPs). Herein, we present the synthesis and characterisation of two new fluorescently labelled vanadyl complexes (14 and 15) with bridged di-picolin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffe499364c0a0fbad50710973da052fe
https://pubmed.ncbi.nlm.nih.gov/27008377
https://pubmed.ncbi.nlm.nih.gov/27008377
Publikováno v:
Journal of chemical biology. 6(4)
Small molecules have long been used for the selective recognition of a wide range of analytes. The ability of these chemical receptors to recognise and bind to specific targets mimics certain biological processes (such as protein–substrate interact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9434199f3574a78b2c50b0e4a742348c
https://pubmed.ncbi.nlm.nih.gov/24432132
https://pubmed.ncbi.nlm.nih.gov/24432132
Autor:
Lok Hang Mak, Katherine A. Scott, Claire Scott, Jessica Knott, Oscar Ces, Gillian F. Whyte, Yu Ye, David J. Mann, James T. Stivers, Rudiger Woscholski
Arylstibonates structurally resemble phosphotyrosine side chains in proteins and here we addressed the ability of such compounds to act as inhibitors of a panel of mammalian tyrosine and dual-specificity phosphatases. Two arylstibonates both possessi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::869cc84fd5125bf71d2190b503f2f8ff
http://hdl.handle.net/10044/1/10092
http://hdl.handle.net/10044/1/10092
