| Literature DB >> 8576194 |
L Désaubry1, I Shoshani, R A Johnson.
Abstract
2',5'-Dideoxyadenosine 3'-di- and triphosphates were tested as inhibitors of brain adenylyl cyclases. With an IC50 approximately 40 nM, 2',5'-dideoxy-3'-ATP is the most potent nonprotein synthetic regulator of adenylyl cyclases thus far described. Neither 2',5'-dideoxy-3'-ADP nor 2',5'-dideoxy-3'-ATP inhibited activity by competition with substrate, and the linear noncompetitive inhibition observed was consistent with interaction via a distinct domain. The availability of this ligand will permit the development of a variety of probes that will be extremely useful in investigating adenylyl cyclase structure and the role(s) that this class of compound may play in physiologically regulating cell function.Entities:
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Year: 1996 PMID: 8576194 DOI: 10.1074/jbc.271.5.2380
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157