Molekülstruktur von P1,P5-Di(adenosine-5') pentaphosphate ammonium salt
P1,P5-Di(adenosine-5′) pentaphosphate ammonium salt
Alternative Namen:
A(5′)P5(5′)A; Diadenosine pentaphosphate ammonium salt
Anwendungen:
P1,P5-Di(adenosine-5′) pentaphosphate ammonium salt is a diadenosine polyphosphate
Reinheit:
≥95%
Molekulargewicht:
916.37
Summenformel:
C20H29N10O22P5•xNH3
Ausschließlich für Forschungszwecke. Nicht Geeignet für Verwendung in Diagnostik oder Therapie.
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P1,P5-Di(adenosine-5′) pentaphosphate ammonium salt Literaturhinweise
Edgecombe, M., et al., Diadenosine polyphosphate-stimulated gluconeogenesis in isolated rat proximal tubules. Biochem. J. 323, 451-456, (1997); Ogilvie, A., et al., Adenine dinucleotides: a novel class of signalling molecules. J. Auton. Pharmacol. 16, 325-328, (1996) Verspohl. E.J., and Johannwille, B., et al., Diadenosine polyphosphates in insulin-secreting cells: interaction with specific receptors and degradation. Diabetes 47, 1727-1734, (1998); Jovanovic, A., et al., Diadenosine 5′,5"-P1,P5-pentaphosphate harbors the properties of a signaling molecule in the heart. FEBS Lett. 423, 314-318, (1998); Pintor, J., and Miras-Portugal, M.T., P2 purinergic receptors for diadenosine polyphosphates in the nervous system. Gen. Pharmacol. 26, 229-235, (1995); Wildman, S.S., et al., Selectivity of diadenosine polyphosphates for rat P2X receptor subunits. Eur. J. Pharmacol. 367, 119-123, (1999); Pintor, J., et al., Presence of dinucleotide and ATP receptors in human cerebrocortical synaptic terminals. Eur. J. Pharmacol. 366, 159-165, (1999); Delaney, S.M., et al., Diadenosine polyphosphates inhibit adenosine kinase activity but decrease levels of endogenous adenosine in rat brain. Eur. J. Pharmacol. 332, 35-42, (1997)Bestellinformation
| Produkt | Katalog # | EINHEIT | Preis | ANZAHL | Favoriten | |
P1,P5-Di(adenosine-5′) pentaphosphate ammonium salt, 10 mg | sc-215657 | 10 mg | $151.00 | |||
P1,P5-Di(adenosine-5′) pentaphosphate ammonium salt, 25 mg | sc-215657A | 25 mg | $288.00 |