AAAAAA

   
Results: 1-3 |
Results: 3
1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro
Authors: Perchellet, EM Magill, MJ Huang, XD Dalke, DM Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., 1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro, ANTI-CANC D, 11(5), 2000, pp. 339-352
Triptycenes: a novel synthetic class of bifunctional anticancer drugs thatinhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro
Authors: Perchellet, EM Magill, MJ Huang, XD Brantis, CE Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., Triptycenes: a novel synthetic class of bifunctional anticancer drugs thatinhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro, ANTI-CANC D, 10(8), 1999, pp. 749-766
Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancerdrugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivo
Authors: Perchellet, EM Ladesich, JB Magill, MJ Chen, Y Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancerdrugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivo, ANTI-CANC D, 10(5), 1999, pp. 489-504
Risultati: 1-3 |