1. GPCR/G Protein Cell Cycle/DNA Damage
  2. P2Y Receptor DNA/RNA Synthesis
  3. Uridine 5'-O-thiodiphosphate

Uridine 5'-O-thiodiphosphate (UDP-β-S) is a P2Y6 receptor agonist with an EC50 of 25 nM. Uridine 5'-O-thiodiphosphate resists degradation by extracellular nucleotidases and stimulates the accumulation of inositol phosphates. Uridine 5'-O-thiodiphosphate stimulates contractile responses in endothelium-denuded rat mesenteric arteries. As a mitogen, Uridine 5'-O-thiodiphosphate stimulates DNA synthesis, [3H] thymidine incorporation, protein synthesis, [3H]leucine incorporation, and increases the number of vascular smooth muscle cells. Uridine 5'-O-thiodiphosphate can be used in the research of cardiovascular diseases such as atherosclerosis.

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Uridine 5'-O-thiodiphosphate

Uridine 5'-O-thiodiphosphate Chemical Structure

CAS No. : 221010-51-1

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Description

Uridine 5'-O-thiodiphosphate (UDP-β-S) is a P2Y6 receptor agonist with an EC50 of 25 nM. Uridine 5'-O-thiodiphosphate resists degradation by extracellular nucleotidases and stimulates the accumulation of inositol phosphates. Uridine 5'-O-thiodiphosphate stimulates contractile responses in endothelium-denuded rat mesenteric arteries. As a mitogen, Uridine 5'-O-thiodiphosphate stimulates DNA synthesis, [3H] thymidine incorporation, protein synthesis, [3H]leucine incorporation, and increases the number of vascular smooth muscle cells. Uridine 5'-O-thiodiphosphate can be used in the research of cardiovascular diseases such as atherosclerosis[1][2].

IC50 & Target[2]

P2Y6 Receptor

25 nM (EC50)

In Vitro

Uridine 5'-O-thiodiphosphate is a potent and selective agonist of the human P2Y6 receptor expressed in 1321N1 cells, with an EC50 of 28 nM, and shows no activity against human P2Y1, P2Y2 or P2Y4 receptors[2].
Uridine 5'-O-thiodiphosphate (1-30 μM; 19 h) stimulates DNA synthesis in rat aortic vascular smooth muscle cells, with an Emax that is 73% higher than that of the control group and a pEC50 of 5.42[2].
Uridine 5'-O-thiodiphosphate (30 μM; 96 h) increases protein synthesis in rat aortic vascular smooth muscle cells by 25% compared with the control group[2].
Uridine 5'-O-thiodiphosphate (30 μM; 0-120 min) is resistant to degradation by nucleotideases in 1321N1 astrocytoma cells over a 120-minute incubation period[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Proliferation Assay[2]

Cell Line: rat aorta vascular smooth muscle cells (VSMC)
Concentration: 1-30 μM
Incubation Time: 19 h
Result: Induced a concentration-dependent increase in [3H]thymidine incorporation, with an Emax of 73% above control and a pEC50 of 5.42.
Stimulated [3H]thymidine incorporation by 36% above control at 1 μM, and showed an additive effect when combined with 1 μM UTPγS.
Stimulated [3H]thymidine incorporation to levels comparable to UDP at 30 μM.
Molecular Weight

420.23

Formula

C9H14N2O11P2S

CAS No.
SMILES

O[C@H]1[C@@H](O)[C@H](N2C=CC(NC2=O)=O)O[C@@H]1COP(OP(O)(S)=O)(O)=O

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Please store the product under the recommended conditions in the Certificate of Analysis.

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Uridine 5'-O-thiodiphosphate
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HY-137608
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