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Chemical Compound Review

AMP-Amidate     amino-[[(2R,3S,4R,5R)-5-(6- aminopurin-9...

Synonyms: AMP-NH2, CHEMBL583986, SureCN1835414, CHEBI:16771, AC1L98RD, ...
 
 
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High impact information on AMP

  • Here we show that rabbit and yeast Hint hydrolyze the natural product adenosine-5'-monophosphoramidate (AMPNH(2)) in an active-site-dependent manner at second order rates exceeding 1,000,000 m(-1) s(-1) [1].
  • In the rabbit mesenteric artery, ATP and adenyl-imidophosphate showed much the same potency in inhibiting the amplitude of e.j.p.s. Therefore, the ATP action on nerve terminals is not due to a high energy requiring mechanism [2].

References

  1. Adenosine monophosphoramidase activity of Hint and Hnt1 supports function of Kin28, Ccl1, and Tfb3. Bieganowski, P., Garrison, P.N., Hodawadekar, S.C., Faye, G., Barnes, L.D., Brenner, C. J. Biol. Chem. (2002) [Pubmed]
  2. The presynaptic regulation of noradrenaline release differs in mesenteric arteries of the rabbit and guinea-pig. Kuriyama, H., Makita, Y. J. Physiol. (Lond.) (1984) [Pubmed]
 
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