Zobrazeno 1 - 10 of 15 pro vyhledávání: '"R. M. Kanojia"'
1
Antibacterial agents that inhibit two-component signal transduction systems
Autor: R. M. Goldschmidt, S. G. Johnson, D. H. Klaubert, L. E. Lawrence, B. Foleno, James A. Hoch, J. P. Demers, R. M. Kanojia, Lei Wang, R. Chen, R. Frechette, A. Donetz, L. Licata, John F. Barrett, J. M. Whiteley, Kwasi A. Ohemeng, D. J. Hlasta, MaryBeth Frosco, J. Bernstein, J. Fernandez, S. Huang, M. J. Macielag
Publikováno v: Proceedings of the National Academy of Sciences. 95:5317-5322
A class of antibacterials has been discovered that inhibits the growth of Gram-positive pathogenic bacteria. RWJ-49815, a representative of a family of hydrophobic tyramines, in addition to being a potent bactericidal Gram-positive antibacterial, inh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06f5c667d49c293cae45ac2a9293f4c7
https://doi.org/10.1073/pnas.95.9.5317
Zobrazit plný text záznamu
2
Synthesis and class III type antiarrhythmic activity of 4-aroyl (and aryl)-l-aralkylpiperazines
Autor: R M, Kanojia, J J, Salata, J, Kauffman
Publikováno v: Bioorganicmedicinal chemistry letters. 10(24)
The synthesis and in vitro Class III antiarrhythmic activity of several 4-aroyl (and aryl)-1-aralkylpiperazine and piperidine derivatives are described. Among several potent compounds identified in the series, RWJ-28810 (3), with its EC20 of 3 nM, ra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4944960c8710ce7a72141c4737a89d7d
https://pubmed.ncbi.nlm.nih.gov/11133100
Zobrazit plný text záznamu
3
Synthesis and SAR of 6-substituted purine derivatives as novel selective positive inotropes
Autor: J B, Press, R, Falotico, Z G, Hajos, R A, Sawyers, R M, Kanojia, L, Williams, B, Haertlein, J A, Kauffman, C, Lakas-Weiss, J J, Salata
Publikováno v: Journal of medicinal chemistry. 35(24)
A series of purine derivatives was prepared and examined for selective inotropic activity in vitro and in vivo. Thioether-linked derivatives were superior to their oxygen and nitrogen isosteres. Substitution of electron-withdrawing groups on the benz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b5f881ba4cf5cd70d8d1ca74078ea1b0
https://pubmed.ncbi.nlm.nih.gov/1335073
Zobrazit plný text záznamu
4
Synthesis and estrogenic properties of 17-epi-ethynylestradiol and its ether derivatives epimestranol and epiquinestrol
Autor: Joanne M. Killinger, J.L. McGuire, R. M. Kanojia, George O. Allen
Publikováno v: Journal of Medicinal Chemistry. 22:1538-1541
The synthesis of 17-epi-ethynylestradiol (10), the 17 beta-ethynyl-17 alpha-ol epimer of the well-known orally active estrogen, ethynylestradiol (1), was achieved by LiA1H4 reduction of epoxide 9, as well as by demethylating epimestranol (11) with CH
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a661daad7f52ce9f605a981895f05073
https://doi.org/10.1021/jm00198a021
Zobrazit plný text záznamu
7
ChemInform Abstract: SYNTHESIS AND ESTROGENIC PROPERTIES OF 17-EPI-ETHYNYLESTRADIOL AND ITS ETHER DERIVATIVES EPIMESTRANOL AND EPIQUINESTROL
Autor: George O. Allen, J.L. McGuire, R. M. Kanojia, Joanne M. Killinger
Publikováno v: Chemischer Informationsdienst. 11
The synthesis of 17-epi-ethynylestradiol (10), the 17 beta-ethynyl-17 alpha-ol epimer of the well-known orally active estrogen, ethynylestradiol (1), was achieved by LiA1H4 reduction of epoxide 9, as well as by demethylating epimestranol (11) with CH
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::51de1c0850f44470581a548a0571911b
https://doi.org/10.1002/chin.198016288
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje