Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yasuko Kiyoi"'
Autor:
Yi Zang, Weiguo Liu, Zhuyan Guo, Yasuko Kiyoi, Eleanor Pow, Lindsay Brown, Charles A. Lesburg, Brian Hawes, Terri M. Kelly, Emma Carswell, Santhosh Neelamkavil, Scott D. Edmondson, Andrew J. Cooke, KehDih Lai, Wayne M. Geissler, Harold B. Wood, Zahid Hussain
Publikováno v:
Bioorganicmedicinal chemistry letters. 30(16)
A series of 4, 4-disubstituted proline analogs were designed, synthesized, and tested for selective inhibition of blood coagulation factor XIa in search of new non-vitamin K antagonists based oral anticoagulants for potential prevention and treatment
Autor:
Anna Marie Easson, Yasuko Kiyoi, Steven Laats, Keneth Davies, Mark Reid, Stuart Francis, Helen Feilden, Grant Wishart, Peter C. Ray, Takao Kiyoi, Duncan McArthur
Publikováno v:
Tetrahedron Letters. 52:3421-3425
Tetrahydro-2H-[2]benzopyrano[3,4-c]pyrrol-3-ones and the related 3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole analogues were synthesised by an intramolecular Diels–Alder reaction. The observed stereoselectivity was dependent upon the natu
Publikováno v:
Tetrahedron Letters. 52:3417-3420
Hexahydro[2]benzopyrano[4,3- c ]pyridines were synthesized by an intramolecular hetero Diels–Alder reaction. The reaction was applicable to a range of substrates and the products could be easily converted into serotonin 5-HT 2C receptor agonists.
Autor:
Takao Kiyoi, Mark Reid, Stuart Francis, Keneth Davies, Steven Laats, Duncan McArthur, Anna-Marie Easson, Yasuko Kiyoi, Gary Tarver, Wilson Caulfield, Kirsty Gibson, Grant Wishart, Angus J. Morrison, Julia M. Adam, Peter Ray
Publikováno v:
Tetrahedron Letters. 52:3413-3416
Autor:
Yasuko Kiyoi, Phillip M. Cowley, Ian Carlyle, James R. Baker, Thomas R. Clarkson, Grant Wishart, Dawn Osbourn, Iain J. Martin, Kirsteen Buchanan, Darren Edwards, Nick Ward, Maureen Deehan, John K. Clark, Glenn Walker
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:2034-2039
The pharmacokinetic based optimisation of a novel series of indole-2-carboxamide antagonists of the cannabinoid CB(1) receptor is disclosed. Compound 24 was found to be a highly potent and selective cannabinoid CB(1) antagonist with high predicted hu
Publikováno v:
ChemInform. 42