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UTP - Solid

Uridine 5'-triphosphate, Trisodium salt trihydrate

Cat. No. Amount Price (EUR) Buy / Note
NU-1013-100 100 mg 50,40 Add to Basket/Quote Add to Notepad
NU-1013-1G 1 g 204,50 Add to Basket/Quote Add to Notepad
NU-1013-10G 10 g 544,70 Add to Basket/Quote Add to Notepad
NU-1013-100G 100 g 1.718,60 Add to Basket/Quote Add to Notepad
Structural formula of UTP - Solid (Uridine 5'-triphosphate, Trisodium salt trihydrate)
Structural formula of UTP - Solid

For research use only!

Shipping: shipped on gel packs

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

Shelf Life: 12 months after date of delivery

Molecular Formula: C9H15N2O15P3 (free acid)

Molecular Weight: 484.14 g/mol (free acid)

CAS#: 19817-92-6

Purity: ≥ 90 % (HPLC)

Form: lyophilised

Color: clear

Spectroscopic Properties: λmax 262 nm, ε 9.8 L mmol-1 cm-1 (Tris-HCl pH 7.0)

Activation of purinergic receptors[1,2,3,4]
Cardioprotection against hypoxic damage[2]
Enzyme kinetic parameters[5]
Phosphorylation of EGF-receptor vie purinergic receptors[3]
Stimulation of neurogenesis and dopaminergic neurons[6]

Specific Ligands:

Enterovirus 71 3D RNA polymerase[7]

Ligand for purinergic receptors:

Quality Control Specifications: in vitro transcription (T7 RNA polymerase): visible RNA fragments after 5 min incubation, DNases, RNases, Nicking Activity: not detectable, Proteases: not detectable

Product Citations:
Please click the black arrow on the right to expand the citation list. Click publication title for the full text.

Selected References:
[1] Raqeeb et al. (2011) Purinergic P2Y2 receptors mediate rapid Ca2+ mobilization, membrane hyperpolarization and nitric oxide production in human vascular endothelial cells. Cell Calcium 49:240.
[2] Golan et al. (2011) Extracellular nucleotide derivatives protect cardiomyocytes against hypoxic stress. Biochemical Pharmacology 81:1219.
[3] Boucher et al. (2011) Distinct activation of epidermal growth factor receptor by UTP contributes to epithelial cell wound repair. American Journal Pathology 178:1092.
[4] Sugihara et al. (2011) Dual signaling pathway of arterial constriction by extracellular uridine-5-triphosphate in the rat. J. Pharmacological Sciences (Japan) 115:293.
[5] Ma et al. (2011) Molecular cloning and analysis of the UDP-glucose pyrophosphorylase in Streptococcus equi subsp. Zooepidemicus. Molecular Biology Reports 38:2751.
[6] Delic et al. (2011) Nucleotides affect neurogenesis and dopaminergic differentiation of mouse fetal midbrain-derived neural precursor cells. Puronergic Signalling 6:417.
[7] Jiang et al. (2011) Biochemical characterization of enterovirus 71 3D RNA polymerase. Biochim. Biophys. Acta, Gene Regulatory Mechanisms 1809:211.
[8] Pendergast et al. (2001) Synthesis and P2Y receptor activity of a series of uridine dinucleoside 5'-polyphosphates. Bioorg. Med. Chem. Lett. 11 (2):157.
[9] Shaver et al. (1997) 4-substituted uridine 5'-triphosphates as agonists of the P2Y2 purinergic receptor. Nucleosides and Nucleotides 16 (7):1099.
[10] Kim et al. (2002) Methanocarba modification of uracil and adenine nucleotides: High potency of northern ring conformation at P2Y1, P2Y2, P2Y4 and P2Y11 but not P2Y6 receptors. J. Med. Chem. 45:208.
[11] Nguyen et al. (1995) Cloning, expression, and chromosomal localization of human uridine nucleotide receptors. J. Biol. Chem. 270 (52):30845.