Publication: Newly synthesized L-enantiomers of 3'-fluoro-modified beta-2'-deoxyribonucleoside 5'-triphosphates inhibit hepatitis B DNA polymerases but not the five cellular DNA polymerases alpha, beta, gamma, delta, and epsilon nor HIV-1 reverse transcriptase.
Newly synthesized L-enantiomers of 3'-fluoro-modified beta-2'-deoxyribonucleoside 5'-triphosphates inhibit hepatitis B DNA polymerases but not the five cellular DNA polymerases alpha, beta, gamma, delta, and epsilon nor HIV-1 reverse transcriptase.
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von Janta-Lipinski, M., Costisella, B., Ochs, H., Hübscher, U., Hafkemeyer, P., & Matthes, E. (1998). Newly synthesized L-enantiomers of 3’-fluoro-modified beta-2’-deoxyribonucleoside 5’-triphosphates inhibit hepatitis B DNA polymerases but not the five cellular DNA polymerases alpha, beta, gamma, delta, and epsilon nor HIV-1 reverse transcriptase. Journal of Medicinal Chemistry, 41(12), 2040–2046. https://doi.org/10.1021/jm9704210
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Novel beta-L-2',3'-dideoxy-3'-fluoro nucleosides were synthesized and further converted to their 5'-triphosphates. Their inhibitory activities against hepatitis B virus (HBV) and duck hepatitis B virus (DHBV) DNA polymerases, human immunodeficiency virus (HIV) reverse transcriptase (RT), and the cellular DNA polymerases alpha, beta, gamma, delta, and epsilon were investigated and compared with those of the corresponding 3'-fluoro-modified beta-d-analogues. The 5'-triphosphates of 3'-deoxy-3'-fluoro-beta-L-thymidine (beta-L-FTTP), 2',3
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- von Janta-Lipinski, M
- Costisella, B
- Ochs, H
- Hübscher, U
- Hafkemeyer, P
- Matthes, E
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Citations
von Janta-Lipinski, M., Costisella, B., Ochs, H., Hübscher, U., Hafkemeyer, P., & Matthes, E. (1998). Newly synthesized L-enantiomers of 3’-fluoro-modified beta-2’-deoxyribonucleoside 5’-triphosphates inhibit hepatitis B DNA polymerases but not the five cellular DNA polymerases alpha, beta, gamma, delta, and epsilon nor HIV-1 reverse transcriptase. Journal of Medicinal Chemistry, 41(12), 2040–2046. https://doi.org/10.1021/jm9704210