SPRi 3
Tocris Bioscience, part of Bio-Techne | Catalog # 6597
Potent sepiapterin reductase (SPR) inhibitor; attenuates proliferation of CD4+ T cells
Key Product Details
Description
Potent sepiapterin reductase (SPR) inhibitor; attenuates proliferation of CD4+ T cells
Product Description
SPRi 3 is a potent sepiapterin reductase (SPR) inhibitor (IC50 = 53 - 74 nM for human SPR). Inhibits BH4 synthesis pathway and attenuates proliferation in naive CD4+ T cells. Suppresses proliferation of human effector CD4+ T cells following stimulation. Reduces SPR activity in mouse primary cultures of sensory neurons (IC50 = 450 nM). Ameliorates colitis, suppressing the intestinal infiltration of T cells and other immune cells in vivo. Also reduces immune-cell infiltration into mouse lungs. Reduces neuropathic and inflammatory pain in mouse models.Licensing Information
Sold under license from the Children's Medical Center Corporation.Product Specifications
Molecular Weight
262.30
Formula
C14H18N2O3
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
N-[2-(5-Hydroxy-2-methyl-1H-indol-3-yl)ethyl]-2-methoxyacetamide
CAS Number
1292285-54-1
PubChem ID
52911386
InChI Key
YBXBWBBVLXZQBJ-UHFFFAOYSA-N
SMILES
COCC(NCCC1=C(NC2=CC=C(C=C12)O)C)=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 26.23 | 100 | |
| Ethanol | 26.23 | 100 |
Preparing Stock Solutions
for SPRi 3
The following data is based on the product molecular weight 262.30
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.81 mL | 19.06 mL | 38.12 mL |
| 5 mM | 0.76 mL | 3.81 mL | 7.62 mL |
| 10 mM | 0.38 mL | 1.91 mL | 3.81 mL |
| 50 mM | 0.08 mL | 0.38 mL | 0.76 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Latremoliere Reduction of neuropathic and inflammatory pain through inhibition of the tetrahydrobiopterin pathway. Neuron 2015 PMID: 26087165
- Cronin The metabolite BH4 controls T cell proliferation in autoimmunity and cancer. Nature 2018 PMID: 30405245
- Haruki Tetrahydrobiopterin biosynthesis as a potential target of the kynurenine pathway metabolite xanthurenic acid. J.Biol.Chem. 2016 PMID: 26565027
Product Specific Notices for SPRi 3
For research use only
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