Zobrazeno 1 - 9
of 9
pro vyhledávání: '"J. J. Jun. Landi"'
Autor:
J. J. Jun. Landi, Carla Manzotti, Mary E. Petry, F. C. Giuliani, Ambrogio Oliva, M. J. Maresch, J. Stallman, Sergio Tognella, M. P. Hacker, S. Spinelli, Ernesto Menta, Zelleka Getahun, J. F. Polsenberg, A. P. Krapcho, C. E. Gallagher, Gino Beggiolin, G. Pezzoni
Publikováno v:
ChemInform. 25
Autor:
J. J. Jun. Landi, S. Spinelli, M. P. Hacker, J. Stallman, J. F. Polsenberg, Mary E. Petry, A. Oliva, R. Di Domenico, A. P. Krapcho, E. Menta
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 29
Autor:
Getahun Z, Petry Me, F. C. Giuliani, M. J. Maresch, Miles P. Hacker, C. E. Gallagher, A. P. Krapcho, J. F. Polsenberg, J. J. Jun. Landi, J. Stallman
Publikováno v:
Journal of medicinal chemistry. 37(6)
Synthetic procedures have been developed which lead to the 2-aza congeners 3 and several related N-oxides 4. The analogues 3 exhibited a wide range of in vitro cytotoxicity against L1210 leukemia, the human colon adenocarcinoma cell line LoVo, and th
Autor:
Miles P. Hacker, J. J. Jun. Landi, John J. McCormack, Donald G. Phinney, A. P. Krapcho, K. J. Shaw
Publikováno v:
Journal of Medicinal Chemistry. 29:1370-1373
A number of unsymmetrically substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been synthesized and evaluated for their antitumor activity against L1210 in vitro and in vivo. The high activity of several compounds observed in vitro was
Publikováno v:
Journal of Medicinal Chemistry. 28:1124-1126
Several 5,8-bis[(aminoalkyl)amino]-1-azaanthracene-9,10-diones have been synthesized and evaluated for antitumor activity against L1210 leukemia both in vitro and in vivo. Comparisons are made to the corresponding carbocyclic analogues. One of the az
Publikováno v:
Chemischer Informationsdienst. 16
Synthese par reaction photochimique de la dimethoxy-1,4 anthraquinone avec des alkylamines, suivie une reaction thermique avec des alkylamines
Autor:
J. J. Jun. Landi, Donald G. Phinney, K. J. Shaw, Miles P. Hacker, John J. McCormack, A. P. Krapcho
Publikováno v:
ChemInform. 18
A number of unsymmetrically substituted 1,4-bis[(aminoalkyl)amino]anthracene-9,10-diones have been synthesized and evaluated for their antitumor activity against L1210 in vitro and in vivo. The high activity of several compounds observed in vitro was
Publikováno v:
Chemischer Informationsdienst. 16
Several 5,8-bis[(aminoalkyl)amino]-1-azaanthracene-9,10-diones have been synthesized and evaluated for antitumor activity against L1210 leukemia both in vitro and in vivo. Comparisons are made to the corresponding carbocyclic analogues. One of the az