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TWO HYDROLASE RESISTANT ANALOGUES OF DIADENOSINE 5′,5′″-P(1),P(3)-TRIPHOSPHATE FOR STUDIES WITH FHIT, THE HUMAN FRAGILE HISTIDINE TRIAD PROTEIN
The design and synthesis of analogues of diadenosine 5′,5′″-P(1),P(3)-triphosphate that are resistant to pyrophosphate hydrolysis is described in relation to their role in signaling and tumorigenesis involving the Fhit protein, the human fragile histidine triad protein, which is a novel Ap3A binding...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
1998
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2556045/ https://ncbi.nlm.nih.gov/pubmed/9708352 |
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