AAAAAA

   
Results: 1-3 |
Results: 3
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. (vol 42, pg 4145, 1999)
Authors: Hogberg, M Sahlberg, C Engelhardt, P Noreen, R Kangasmetsa, J Johansson, NG Oberg, B Vrang, L Zhang, H Sahlberg, BL Unge, T Lovgren, S Fridborg, K Backbro, K
Citation: M. Hogberg et al., Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. (vol 42, pg 4145, 1999), J MED CHEM, 43(2), 2000, pp. 304-304
Substrate/inhibitor properties of human deoxycytidine kinase (dCK) and thymidine kinases (TK1 and TK2) towards the sugar moiety of nucleosides, including O '-alkyl analogues
Authors: Kierdaszuk, B Krawiec, K Kazimierczuk, Z Jacobsson, U Johansson, NG Munch-Petersen, B Eriksson, S Shugar, D
Citation: B. Kierdaszuk et al., Substrate/inhibitor properties of human deoxycytidine kinase (dCK) and thymidine kinases (TK1 and TK2) towards the sugar moiety of nucleosides, including O '-alkyl analogues, NUCLEOS NUC, 18(8), 1999, pp. 1883-1903
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues
Authors: Hogberg, M Sahlberg, C Engelhardt, P Noreen, R Kangasmetsa, J Johansson, NG Oberg, B Vrang, L Zhang, H Sahlberg, BL Unge, T Lovgren, S Fridborg, K Backbro, K
Citation: M. Hogberg et al., Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues, J MED CHEM, 42(20), 1999, pp. 4150-4160
Risultati: 1-3 |