Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fatemeh Olang"'
Autor:
Wen Cai, Mary Hassani, Nicholas G. Hermann, Anthony S. Rose, Jennifer S. Lucas, Thomas J. Eads, Ervin D. Walter, Minoo Sedighi, Sahba Charkhzarrin, Katherine H. Koelsch, Mohammad Behforouz, Hamid Mirzaei, Fatemeh Olang, Howard D. Beall, Hassan Seradj, Rajesh Karki, Jayana P. Lineswala, Jeremy S. York
Publikováno v:
Bioorganic & Medicinal Chemistry. 18:1899-1909
A series of lavendamycin analogues with two, three or four substituents at the C-6, C-7 N, C-2′, C-3′ and C-11′ positions were synthesized via short and efficient methods and evaluated as potential NAD(P)H:quinone oxidoreductase (NQO1)-directed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1216665b2bf05aa18601a35f725778f6
https://doi.org/10.1016/j.bmc.2010.01.037
https://doi.org/10.1016/j.bmc.2010.01.037
Autor:
Howard D. Beall, Jayana P. Lineswala, William Glen Holloway, Wen Cai, Fatemeh Olang, Mohammad Behforouz, John M. Gerdes, Katherine H. Koelsch, David C. Holley, Mary Hassani, Anthony S. Rose
Publikováno v:
Journal of Medicinal Chemistry. 51:3104-3115
A 1H69 crystal structure-based in silico model of the NAD(P)H:quinone oxidoreductase 1 (NQO1) active site has been developed to facilitate NQO1-directed lavendamycin antitumor agent development. Lavendamycin analogues were designed as NQO1 substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b17e014a7ec0d780a03a98a1fd2fa12
https://doi.org/10.1021/jm701066a
https://doi.org/10.1021/jm701066a
Autor:
Mary Hassani, Wen Cai, Katherine H. Koelsch, David C. Holley, Anthony S. Rose, Fatemeh Olang, Jayana P. Lineswala, William G. Holloway, John M. Gerdes, Mohammad Behforouz, Howard D. Beall
Publikováno v:
Journal of Medicinal Chemistry; May2008, Vol. 51 Issue 11, p3104-3115, 12p