AP5G

P1-(5'-Adenosyl) P5-(5'-guanosyl) pentaphosphate, Triethylammonium salt

Catálogo Nº Apresentação Preço (R$) Comprar
NU-504S 50 μl (10 mM)Sob demanda Adicionar ao Carrinho
NU-504L 5 x 50 μl (10 mM)Sob demanda Adicionar ao Carrinho
Structural formula of AP5G (P1-(5'-Adenosyl) P5-(5'-guanosyl) pentaphosphate, Triethylammonium salt)
Structural formula of AP5G

For general laboratory use.

Envio: shipped on gel packs

Condições de armazenamento: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Validade: 12 months after date of delivery

Fórmula molecular: C20H29N10O23P5 (free acid)

Peso molecular: 932.37 g/mol (free acid)

CAS#: 56983-24-5

Pureza: ≥ 95 % (HPLC)

Forma: solution in water

Concentração: 10 mM - 11 mM

pH: 7.5 ±0.5

Propriedades espectroscópicas: λmax 259 nm, ε 27.0 L mmol-1 cm-1 (Tris-HCl pH 7.5)

Formulários:
Substrate replacement at UMP-CMP kinase[1]
Crystal structure of complex with GMP kinase[2]
Vasoconstriction via activation of P2X-receptors[3]
Activation of P2X receptor ion channels[4]

Specific Ligands:

Binding to purinoreceptors P2Y1 and P2X[5]

Binding to purinoreceptors P2X3 and rP2X1[6]

Referências selecionadas:
[1] Topalis et al. (2007) Nucleotide binding to human UMP-CMP kinase using fluorescent derivatives -- a screening based on affinity for the UMP-CMP binding site. FEBS J. 274 (14):3704.

[2] Hible et al. (2006) Crystal structures of GMP kinase in complex with ganciclovir monophosphate and Ap5G. Biochimie 88:1157.

[3] van der Giet et al. (2001) The critical role of adenosine and guanosine in the affinity of dinucleoside polyphosphates to P (2X)-receptors in the isolated perfused rat kidney. Br. J. Pharmacol. 132 (2):467.

[4] Lewis et al. (2000)Effects of diadenosine polyphosphates (Ap (n)As) and adenosine polyphospho guanosines (Ap (n)Gs) on rat mesenteric artery P2X receptor ion channels.Br. J. Pharmacol. 129 (1):124.

[5] van der Giet et al. (2002) Effects of dinucleoside polyphosphates on regulation of coronary vascular tone. Eur. J. Pharmacol. 448 (2-3):207.

[6] Cinkilic et al. (2001) Selective agonism of group I P2X receptors by dinucleotides dependent on a single adenine moiety. J. Pharmacol. Exp. Ther. 299 (1):131.

Winward et al. (2010) Oxidation of the diphosphoinositol polyphosphate phosphohydrolase-like Nudix hydrolase Aps from Drosophila melanogaster induces thermolability--A possible regulatory switch≥ Int. J. Biochem. Cell Biol. 42 (7):1174.

Safrany et al. (2007) Characterisation of a bis (5'-nucleosyl)-tetraphosphatase (asymmetrical) from Drosophila melanogaster. Int. J. Biochem. Cell Biol. 39 (5):943.

Cherfils et al. (2006) Crystal structures of GMP kinase in complex with ganciclovir monophosphate and Ap5G. Biochimie 88 (9):1157.

Gross et al. (2006) Nucleotide-binding domains of Cystic Fibrosis Transmembrane Conductance Regulator, an ABC Transporter, Catalyze Adenylate Kinase Activity but not ATP Hydrolysis. J. Biol. Chem. 281 (7):4058.

Leslie et al. (2002) Cloning and characterisation of hAps1 and hAps2, human diadenosine polyphosphate-metabolising Nudix hydrolases. BMC Biochemistry 3:20.

Prinz et al. (1999) Binding of nucleotides to guanylate kinase, p21 (ras), and nucleoside-diphosphate kinase studied by nano-electrospray mass spectrometry. J. Biol. Chem. 274 (50):35337.

Ortiz et al. (1993) Specific synthesis of adenosine (5')tetraphospho (5')nucleoside and adenosine- (5')oligophospho (5')adenosine (n > 4) catalyzed by firefly luciverase. Eur. J. Biochem. 212 (1):263.

Feldhaus et al. (1975) Synthetic Inhibitors of Adenylate Kinases in the Assays for ATPases and Phosphokinases. Eur. J. Biochem. 57:197.