Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fraser Hunt"'
Autor:
Stuart Thomas Onions, Harry Finch, Christopher Sleigh, Damien Crepin, John Murray, Euan A. F. Fordyce, John King-Underwood, S. Fraser Hunt, Guillaume F. Parra
Publikováno v:
MedChemComm
Atropisomeric drug substances are known to have different biological properties. Compounds containing the N-benzoylbenzazepine motif have been shown to exhibit energetically restricted rotation around the Ar(CO)N axis. Herein we report, for the first
Autor:
S. Fraser Hunt, Peter Strong, John King-Underwood, Matthew Coates, Jennifer A. Stockwell, Vladimir Sherbukhin, Daniel W. Brookes, Stuart Thomas Onions, Claire Lise-Ciana, Kazuhiro Ito, John Murray, Euan A. F. Fordyce, Guillaume F. Parra, Garth Rapeport, Jennifer C. Thomas
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:2201-2206
The development of novel non-nucleoside inhibitors of the RSV polymerase complex is of significant clinical interest. Compounds derived from the benzothienoazepine core, such as AZ-27, are potent inhibitors of RSV viruses of the A-subgroup, but are o
Autor:
Euan A. F. Fordyce, S. Fraser Hunt, Damien Crepin, Stuart T. Onions, Guillaume F. Parra, Chris J. Sleigh, John King-Underwood, Harry Finch, John Murray
Publikováno v:
MedChemComm. 9(4)
Atropisomeric drug substances are known to have different biological properties. Compounds containing the N-benzoylbenzazepine motif have been shown to exhibit energetically restricted rotation around the Ar(CO)N axis. Herein we report, for the first
Autor:
John P. DeVincenzo, Young-In Kim, Guillaume F. Parra, Daniel W. Brookes, Euan A. F. Fordyce, Claire-Lise Ciana, Vladimir Sherbukhin, Kazuhiro Ito, Pete Strong, Jennifer A. Stockwell, Garth Rapeport, Matthew Coates, Peter John Murray, S. Fraser Hunt, Elizabeth A. Meals, Lindsey Cass, Jennifer C. Thomas, Thomas Colley, Stuart Thomas Onions, Lauren Anderson-Dring, Heather Allen
Publikováno v:
Antimicrobial Agents and Chemotherapy
Although respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infection in infants and young children, attempts to develop an effective therapy have so far proved unsuccessful. Here we report the preclinical profiles
Autor:
David Donald, Lilian Alcaraz, Daniel J. Warner, Nicholas Kindon, Andrew Bailey, Michael J. Stocks, Garry Pairaudeau, Keith Bowers, Jill Theaker, Fraser Hunt, Helen Edwards
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:7458-7461
The optimisation of a new series of high potency muscarinic M3 antagonists, derived from high throughput screening library hit is described.
Autor:
Simon Barber, John Unitt, David Laughton, Fraser Hunt, Sarah King, Bob Thong, Andrew Baxter, Denise Grice, Alastair J. H. Brown, Garry Pairaudeau, Hitesh J. Sanganee, Richard J. Weaver
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:1143-1147
A novel series of small molecule C5a antagonists is reported. In particular, in vitro metabolic studies and solution based combinatorial synthesis are demonstrated as useful tools for the rapid identification of antagonists with low in vitro clearanc
Autor:
Fordyce, Euan A. F., Fraser Hunt, S., Crepin, Damien, Onions, Stuart T., Parra, Guillaume F., Sleigh, Chris J., King-Underwood, John, Finch, Harry, Murray, John
Publikováno v:
MedChemComm; Mar2018, Vol. 9 Issue 3, p583-589, 7p
Autor:
Mark I Christie, Roger Bonnert, Mark Ebden, Peter Cage, Iain Walters, Fraser Hunt, Shirley Lewis, Caroline Austin, Caroline Grahames, David J. Nicholls, Rupert P. Austin, Robert Jewell, Steven Hill, Iain J. Martin, David J. Robinson, Stuart Gardiner
Publikováno v:
Bioorganicmedicinal chemistry letters. 18(2)
The CXCR2 SAR of a series of bicyclic antagonists such as the 2-aminothiazolo[4,5-d]pyrimidine 3b was investigated by systematic variation of the fused pyrimidine-based heterocyclic cores. Replacement of the aminothiazole ring with a 2-thiazolone alt
Autor:
Clare Dixon, David J. Robinson, Mark I Christie, Steven Hill, Jadeen Christie, Ian Martin, Rupert P. Austin, Robert Jewell, Paul Willis, Peter Cage, Caroline Austin, Fraser Hunt, Roger Bonnert
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(10)
As part of a Lead Optimisation programme to identify small molecule antagonists of the human CXCR2 receptor, a series of substituted thiazolo[4,5-d]pyrimidines was prepared via the application of a novel tandem displacement reaction.
Autor:
Kevin J. Edwards, Jorge Rolland Calvo, Berta Martínez Silva, Rodrigo de Balbín Behrmann, Ignacio Montero Ruiz, Charles-Tanguy Le Roux, Manuel Alberto Fernández Götz, Emili Junyent, Xosé-Lois Armada Pita, Brendan O’Connor, Fraser Hunter, Teresa Chapa Brunet, Isabel Izquierdo Peraile
Publikováno v:
Trabajos de Prehistoria, Vol 65, Iss 1, Pp 181-200 (2008)
Externí odkaz:
https://doaj.org/article/895ef61b91014d31a0625e55fefae470