Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stephen Elder"'
Autor:
Stephen Elder
The Shining Man and his wife return on another mission. When Filiae Mundi, a wealthy but secretive organization, nominates Elaine to its governing Council, Frank and Elaine go to Washington, a nexus of power and multilayered danger. Elaine proposes a
Autor:
Nigel J. P. Broom, John Stephen Elder, Nicky D. Masson, Isobel Bennett, Robert Cassels, Peter J. O'Hanlon
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:1847-1852
A series of beta-diketone acrylate bioisosteres 4 of pseudomonic acid A 1 have been synthesized and evaluated for their ability to inhibit bacterial isoleucyl-tRNA synthetase and act as antibacterial agents. A number of analogues have excellent antib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0bd12d52c61bcbbe24ba7765ed82dcc
https://doi.org/10.1016/s0960-894x(99)00296-6
https://doi.org/10.1016/s0960-894x(99)00296-6
Publikováno v:
Journal of Nonverbal Behavior. 20:213-228
Sixteen male and sixteen female student observers were shown computer-simulated sequences of male and female head movement based on time-series protocols of real-life interactions and were asked to rate their impressions of the computer actors on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9bb721a6591bc0db1f288d6da486f36
https://doi.org/10.1007/bf02248674
https://doi.org/10.1007/bf02248674
Autor:
J. M. Wilson, Andrew Keith Forrest, John Stephen Elder, Neil D. Pearson, Philippa A. Coates, Angela Abson, Nicky D. Masson, Peter J. O'Hanlon, Nigel J. P. Broom, Amanda J. Hicks, Peter Charles Thomas Hannan, J. E. Pons
Publikováno v:
The Journal of Antibiotics. 49:390-394
The synthesis, antibacterial activities, murine pharmacokinetic and infection model data for a range of aryl and heteroaryl ketone derivatives of monic acid (2a) are reported. The best results were found for the 3-furyl and 2-methoxy thiazol-5-yl ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d863a8b406d31ac36f85500de969a4d
https://doi.org/10.7164/antibiotics.49.390
https://doi.org/10.7164/antibiotics.49.390
Autor:
Andrew Keith Forrest, Neil D. Pearson, Peter Charles Thomas Hannan, Angela Abson, Peter J. O'Hanlon, Philippa A. Coates, Nicky D. Masson, J. E. Pons, John Stephen Elder, Amanda J. Hicks, J. M. Wilson, Nigel J. P. Broom
Publikováno v:
ChemInform. 27
The synthesis, antibacterial activities, murine pharmacokinetic and infection model data for a range of aryl and heteroaryl ketone derivatives of monic acid (2a) are reported. The best results were found for the 3-furyl and 2-methoxy thiazol-5-yl ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2f8c89b5a311e694204c949f84ea662
https://doi.org/10.1002/chin.199639261
https://doi.org/10.1002/chin.199639261
Autor:
Nigel J. P. Broom, John Stephen Elder, Isobel Bennett, Robert Cassels, Peter J. O'Hanlon, Nicky D. Masson
Publikováno v:
ChemInform. 30
A series of beta-diketone acrylate bioisosteres 4 of pseudomonic acid A 1 have been synthesized and evaluated for their ability to inhibit bacterial isoleucyl-tRNA synthetase and act as antibacterial agents. A number of analogues have excellent antib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c52e69c21f99766d910754021a81883c
https://doi.org/10.1002/chin.199943264
https://doi.org/10.1002/chin.199943264
Autor:
John Stephen Elder, ∇ Hung-Yuan Cheng, Nigel J. P. Broom, and Andrew Pope, Peter Charles Thomas Hannan, Nicki Masson, Peter J. O'hanlon, Robert Cassels, J. M. Wilson
Publikováno v:
Journal of medicinal chemistry. 39(18)
A series of C-1 oxazole isosteres of pseudomonic acid A (mupirocin) bearing a nitroheterocycle have been synthesized, and significant differences in both spectrum of activity and potency were found between these derivatives and mupirocin. Additionall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e6aa63b75a317ca6e7859b15761053
https://pubmed.ncbi.nlm.nih.gov/8784459
https://pubmed.ncbi.nlm.nih.gov/8784459