Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Stuart A. Wells"'
Autor:
Brian R. Blais, Stuart A. Wells, Bradley M. Poynter, Tara R. Harris, Ruth A. Allard, John L. Koprowski
Publikováno v:
Zoo Biology. 42:429-439
Zoo-based (ex situ) conservation breeding programs provide invaluable opportunities to uncover enigmatic behaviors and traits of focal species under managed care, which can support research and conservation management efforts. A suite of factors and
Autor:
Brian R. Blais, Stuart A. Wells, Bradley M. Poynter, John L. Koprowski, Michael M. Garner, Ruth A. Allard
Publikováno v:
Zoo biologyREFERENCES. 41(4)
Mimicking natural parameters and complexities in zoo conservation breeding programs can facilitate natural physiological and behavioral traits, which in turn can inform more effective species reintroduction efforts. To curtail population declines of
Publikováno v:
Conservation Genetics. 19:309-322
The amphibian disease chytridiomycosis, caused by the fungus Batrachochytrium dendrobatidis (Bd), has contributed to the decline of Chiricahua leopard frogs (Rana chiricahuensis), a federally threatened species native to the Southwestern United State
Autor:
Ruth A. Allard, Stuart A. Wells
Publikováno v:
The Ark and Beyond ISBN: 9780226538464
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78648edfaa34a4e189809c511e2da305
https://doi.org/10.7208/chicago/9780226538631.003.0014
https://doi.org/10.7208/chicago/9780226538631.003.0014
Autor:
John S. Shaw, Martin Wild, Dearg S. Brown, Howard Tucker, Adrian John Highton, Alan Wellington Faull, John Oldfield, John G. Cumming, Colin Fielding, Stuart L. Wells
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:1655-1659
Modifications to a series of potent and selective substituted 1-(3,3-diphenylpropyl)-piperidine phenylacetamide CCR5 antagonists were explored with the aim of reducing affinity at the hERG cardiac ion channel. Replacement of one aromatic ring in the
Autor:
Neil Rankine, Linda J. Wood, Galith Karoutchi, Michelle Coulson, Keith Oldham, Emma V. Jones, Paul A. Bethel, Stephan Krapp, Susannah J. Ford, Stefan Gerhardt, David Ryan, Matthew Grist, Peter W. Kenny, Hannes Simader, Andrew David Morley, Stuart L. Wells, Gordon A. Hamlin, Stefan Steinbacher, Jack E. Dawson, Nabil Asaad, Martin Augustin, Michael James
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:4280-4283
A series of potent Cathepsin L inhibitors with good selectivity with respect to other cysteine Cathepsins is described and SAR is discussed with reference to the crystal structure of a protein-ligand complex.
Autor:
Peter Ballard, Michael James, Daniel S. James, Peter D. Smith, Simon J. Brown, M. Raymond V. Finlay, Michael J. Waring, Paula Perkins, Andrew D. Campbell, Heather L. McFarland, David Perkins, Gordon S. Currie, Gillian M. Lamont, Graham Richmond, Matthew R. Box, David Whittaker, Mark J. Anderton, Richard A. Ward, Teresa Klinowska, Scott G. Lamont, Nicola Colclough, Stuart L. Wells, Darren Cross, Gail L. Wrigley, George B. Hill, Nathaniel G. Martin, Paul D. Kemmitt, Susan Ashton, Lorraine A. Hassall, Paul A. Bethel, Robert Hugh Bradbury, Sam Butterworth, Christopher G. Chorley, Martine J. Mellor, Matthew Grist, Jonathon P. Orme
Publikováno v:
Journal of medicinal chemistry. 57(20)
Epidermal growth factor receptor (EGFR) inhibitors have been used clinically in the treatment of non-small-cell lung cancer (NSCLC) patients harboring sensitizing (or activating) mutations for a number of years. Despite encouraging clinical efficacy
Autor:
Fredrik Edfeldt, John G. Cumming, Stuart L. Wells, Martin Harrison, Scott G. Lamont, Michael James, Emma Evertsson, Keith Oldham, Jane E. Sullivan, Geoffrey A. Holdgate, Judit E. Debreczeni
Publikováno v:
Journal of medicinal chemistry. 58(1)
Two structurally distinct series of novel, MAPK-activated kinase-2 prevention of activation inhibitors have been discovered by high throughput screening. Preliminary structure-activity relationship (SAR) studies revealed substructural features that i
Autor:
Joanne Wilson, J. Matthew Wood, A. Nigel Brooks, Hill Kathryn Jane, Alfred A. Rabow, Graeme Walker, Andrew G. Thomason, Barry R. Hayter, Nicholas J. Howe, Stuart L. Wells, Glenn Hatter, David A. Jude, Sarah A. Loddick, Gorkhn Sharma-Singh, Scott G. Lamont, Heather L. McFarland, Dawn Trueman, Natalie Stratton, Zaieda Parveen, Nicola Broadbent, Carr Gregory Richard, David G. Acton, Robert Hugh Bradbury, Rhys D.O. Jones
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(7)
Removal of the basic piperazine nitrogen atom, introduction of a solubilising end group and partial reduction of the triazolopyridazine moiety in the previously-described lead androgen receptor downregulator 6-[4-(4-cyanobenzyl)piperazin-1-yl]-3-(tri
Publikováno v:
ChemInform. 32
Much higher yields were found after shorter reaction times for the meta -substituted amination of benzenes in DMPU with microwave heating in a sealed tube (180°C, 5 h), e.g. piperidine and m -fluorobenzonitrile 1 gave the m -substituted 3 in 92% yie