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pro vyhledávání: '"Alex Groarke"'
Autor:
Allan Hallett, Alyson Fox, Moh Panesar, Stuart Bevan, Andrew James Culshaw, Elliot Lilley, Peter McIntyre, Mark Nash, Alex Groarke
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 342:389-398
The therapeutic potential of transient receptor potential vanilloid type 1 (TRPV1) antagonists for chronic pain has been recognized for more than a decade. However, preclinical and clinical data revealed that acute pharmacological blockade of TRPV1 p
Autor:
Alyson Fox, Marcus Peacock, Alice Chen, Alex Groarke, Christopher Thomas Brain, Yvonne Loong, Jean-Philippe Courade, Alex Dyson, Mohammed Yaqoob
Publikováno v:
Pain. 116:129-137
CT-3 (ajulemic acid) is a synthetic analogue of a metabolite of Delta9-tetrahydrocannabinol that has reported analgesic efficacy in neuropathic pain states in man. Here we show that CT-3 binds to human cannabinoid receptors in vitro, with high affini
Autor:
Jon K. Chambers, Laura R. Fitzgerald, Shelagh Wilson, Philip G. Szekeres, Nabil Elshourbagy, Usman Shabon, Dulcie B. Schmidt, George M. Dytko, Nicholas A. Evans, Derk J. Bergsma, Robert S. Ames, Kong B. Tan, Henry M. Sarau, Da Yuan Wang, Graeme Milligan, D. Alex Groarke, Peter T. Buckley, Paul R. Murdock, James J. Foley, Parvathi Nuthulaganti
Publikováno v:
Journal of Biological Chemistry. 275:25965-25971
Opiate tolerance and dependence are major clinical and social problems. The anti-opiate neuropeptides FF and AF (NPFF and NPAF) have been implicated in pain modulation as well as in opioid tolerance and may play a critical role in this process, altho
Autor:
Hart Terance William, Kara McNair, Isabelle Lyothier, Christopher Thomas Brain, Marcus Peacock, Paul R. Coote, and Mohammed Yaqoob, Iain F. James, Luigi La Vecchia, Adam Kesingland, Jiri Zadrobilek, Edward K. Dziadulewicz, Ulrich Schopfer, Werner Huber, Andrew James Culshaw, Adrian J. Fisher, Lee Edwards, Alyson Fox, Portmann Robert, † Cathal O'Farrell, Alex Groarke, Stuart Bevan, Andrew J. Davis, Clive Gentry, Yvonne Loong
Publikováno v:
Journal of medicinal chemistry. 50(16)
Selective activation of peripheral cannabinoid CB1 receptors has the potential to become a valuable therapy for chronic pain conditions as long as central nervous system effects are attenuated. A new class of cannabinoid ligands was rationally design
Publikováno v:
FEBS letters. 419(1)
A fusion protein was constructed between the porcine alpha2A-adrenoceptor and a pertussis toxin-insensitive (Cys351Gly) form of the alpha subunit of the G protein Gi1. Addition of agonist ligands to membranes of COS-7 cells transiently transfected to
Autor:
Edward K. Dziadulewicz, Stuart J. Bevan, Christopher T. Brain, Paul R. Coote, Andrew J. Culshaw, Andrew J. Davis, Lee J. Edwards, Adrian J. Fisher, Alyson J. Fox, Clive Gentry, Alex Groarke, Terance W. Hart, Werner Huber, Iain F. James, Adam Kesingland, Luigi La Vecchia, Yvonne Loong, Isabelle Lyothier, Kara McNair, Cathal O'Farrell
Publikováno v:
Journal of Medicinal Chemistry; Aug2007, Vol. 50 Issue 16, p3851-3856, 6p
Publikováno v:
Biochemical Society Transactions. 21:227S-227S
Akademický článek
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