SCH 202676 hydrobromide
Tocris Bioscience | Catalog # 1400
Key Product Details
Description
Product Description
SCH 202676 hydrobromide is a sulphydryl-reactive compound that inhibits agonist and antagonist binding to G-protein-coupled receptors. Inhibits a variety of GPCRs including adenosine, opioid, muscarinic, adrenergic and dopaminergic receptors (IC50 values are 0.1-1.8 μM).
Product Specifications for SCH 202676 hydrobromide
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
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 | 8.71 | 25 with gentle warming |
Preparing Stock Solutions for SCH 202676 hydrobromide
The following data is based on the product molecular weight 348.26.
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 |
|---|---|---|---|
| 0.25 mM | 11.49 mL | 57.43 mL | 114.86 mL |
| 1.25 mM | 2.30 mL | 11.49 mL | 22.97 mL |
| 2.5 mM | 1.15 mL | 5.74 mL | 11.49 mL |
| 12.5 mM | 0.23 mL | 1.15 mL | 2.30 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 54 publications citing the usage of this product.
- Gao Effects of the allosteric modulator SCH-202676 on adenosine and P2Y receptors. Life Sci. 2004 PMID: 15081581
- Lewandowicz The 'allosteric modulator' SCH-202676 disrupts G protein-coupled receptor function via sulphydryl-sensitive mechanisms. Br.J.Pharmacol. 2006 PMID: 16402041
- Fawzi SCH-202676: an allosteric modulator of both agonist and antagonist binding to G protein-coupled receptors. Mol.Pharmacol. 2001 PMID: 11125021
Product Documents for SCH 202676 hydrobromide
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for SCH 202676 hydrobromide
For research use only
Citations for SCH 202676 hydrobromide
Customer Reviews for SCH 202676 hydrobromide (1)
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Assay Type: In VitroCell Line/Tissue: HepatocyteVerified Customer | Posted 10/25/2018Used as GPCR inhibitor for Glucagon treatment in mouse primary hepatocytes. As shown in the picture, from left to right, 1st sample is untreated, 2nd sample was treated with Glucagon, 3rd sample was pre-treated with this chemical plus glucagon, seems pretty effective for inhibiting glucagon stimulated p-CREB activation. however this chemical is not very stable, seems to loose effectiveness after short storage. Overall is happy with this product.
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