Two Hydrolase Resistant Analogues of Diadenosine 5′,5″′-P,P-Triphosphate for Studies with FHIT, The Human Fragile Histidine Triad Protein
The design and synthesis of analogues of diadenosine 5′,5″′-P,P-triphosphate that are resistant to pyrophosphate hydrolysis is described in relation to their rôle in signalling and tumorigenesis involving the Fhit protein, the human fragile histidine triad protein, which is a novel Ap3A binding/clea...
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Veröffentlicht in: | Nucleosides & nucleotides 1998-01, Vol.17 (1-3), p.301-308 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The design and synthesis of analogues of diadenosine 5′,5″′-P,P-triphosphate that are resistant to pyrophosphate hydrolysis is described in relation to their rôle in signalling and tumorigenesis involving the Fhit protein, the human fragile histidine triad protein, which is a novel Ap3A binding/cleaving protein.
Dedicated to the memory of Professor Tsujiaki Hata, friend and associate for many years, who himself held a close interest in diadenosine and diguanosine polyphosphates. |
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ISSN: | 0732-8311 1525-7770 |
DOI: | 10.1080/07328319808005178 |