Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Maria Ludwikow"'
Autor:
Aesop Cho, David C. Griffith, Lee Chong, Nadeem Iqbal, Padmapriya Kumaraswamy, Uma Oza, Michael N. Dudley, Karen Lolans, Maria Ludwikow, David J. Loury, Shuang Bai, Rajeshwar Singh, Andrea Blecken, Ramona Hilgenkamp, William J. Watkins, Olga Lomovskaya, Deidre Madsen, John Barnard, Negar Garizi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:2802-2806
Further structure–activity relationships of a novel series of fungal efflux pump inhibitors with respect to potentiation of the activity of fluconazole against strains of C. albicans and C. glabrata over-expressing ABC-type efflux pumps are systema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628a6863d6295590a8c587fda7e7591c
https://doi.org/10.1016/j.bmcl.2007.02.047
https://doi.org/10.1016/j.bmcl.2007.02.047
Autor:
Aesop Cho, Nadeem Iqbal, Bonnie Kuo, Karen Lolans, Deidre Madsen, William J. Watkins, Negar Garizi, Rémy C. Lemoine, Renata Jankowska, Vickie Wong, Maria Ludwikow, Rajeshwar Singh, John Barnard, Lee Chong, Uma Oza, Michael N. Dudley, Thomas E. Renau, Olga Lomovskaya
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:5133-5137
Structure-activity relationships of a novel series of fungal efflux pump inhibitors with respect to potentiation of the activity of fluconazole against strains of Candida albicans and Candida glabrata over-expressing ABC-type efflux pumps are systema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a828ac29246edd22634c41ef6029772b
https://doi.org/10.1016/j.bmcl.2004.07.071
https://doi.org/10.1016/j.bmcl.2004.07.071
Autor:
David A. Griffith, Scott J. Hecker, Keith Huie, Aesop Cho, Johanne Blais, Maria Ludwikow, Michael N. Dudley, Tomasz W. Glinka
Publikováno v:
Bioorganic & Medicinal Chemistry. 11:591-600
SAR studies in a series of related 3-(heteroarylthio)cephems determined that a relatively high chemical reactivity of the beta-lactam ring, modulated by electronic effects of substituents at C-3 and C-7, is necessary to achieve high in vitro activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b50a0a557dd4d539d952907fc158202
https://doi.org/10.1016/s0968-0896(02)00431-5
https://doi.org/10.1016/s0968-0896(02)00431-5
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:137-140
Incorporation of a basic aminopyridine into the C-7 position of 3-(amine-substituted arylthio)-3-norcephalosporins, as in 3, afforded high potency against MRSA and acceptable solubility for intravenous administration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d7934a6698b8741b969f8d0d19f691d
https://doi.org/10.1016/s0960-894x(00)00603-x
https://doi.org/10.1016/s0960-894x(00)00603-x
Autor:
Renyi Wang, Russell H. Schmehl, Chong K. Ryu, Jon W. Merkert, Christine E. L. Headford, Maria Ludwikow, C. Michael Elliott, Sue Ferrere
Publikováno v:
Journal of the American Chemical Society. 114:430-438
Intramolecular photoinduced electron transfer in a series of linked ruthenium(II) diimine donor-diquat acceptor complexes was examined as a function of the nature of the bridge between the donor and acceptor centers. Bridging groups include polymethy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59ec279070b58206a7f2b4c3a9416286
https://doi.org/10.1021/ja00028a006
https://doi.org/10.1021/ja00028a006
Publikováno v:
ChemInform. 32
Incorporation of a basic aminopyridine into the C-7 position of 3-(amine-substituted arylthio)-3-norcephalosporins, as in 3, afforded high potency against MRSA and acceptable solubility for intravenous administration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a73f606254442d2538a85bad5044519
https://doi.org/10.1002/chin.200116238
https://doi.org/10.1002/chin.200116238
Publikováno v:
Organic Preparations and Procedures International. 11:275-280
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c81a28f2361dacf81544e07f48baf1
https://doi.org/10.1080/00304947909355411
https://doi.org/10.1080/00304947909355411
Publikováno v:
Journal of Heterocyclic Chemistry. 17:393-395
Dans cette note, nous decrivons brievement quelques resultats permettant de cerner l'utilisation de la catalyse par transfert de phase dans les reactions d'heterocyclisation. Des reactifs dihalogenes sont utilises, les anions engages dans la substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b95f485335be48d07ebb5a2936a85fd6
https://doi.org/10.1002/jhet.5570170237
https://doi.org/10.1002/jhet.5570170237
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b754b4d41658370f91f1a748749d516a
https://doi.org/10.1002/chin.197723135
https://doi.org/10.1002/chin.197723135
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc671f7fd4b648c1fbbe29bf83484155
https://doi.org/10.1002/chin.197814105
https://doi.org/10.1002/chin.197814105