Suramin hexasodium salt
Tocris Bioscience, part of Bio-Techne | Catalog # 1472
Non-selective P2 antagonist
Product Description
Suramin hexasodium salt is a non-selective P2 purinergic antagonist. Also blocks calmodulin binding to recognition sites and G protein coupling to G protein-coupled receptors. Increases open probability of ryanodine receptor (RyR) channels and acts as a competitive α1β2γ2 GABAA receptor antagonist. Anticancer, antiviral and antiparasitic agent.This product may be supplied with a high degree of hydration and some residual NaCl, the amounts of which are batch dependent. Please refer to the Certificate of Analysis to obtain the batch specific Net Product Content.
Product Specifications
Molecular Weight
1429.15
Formula
C51H34N6Na6O23S6
Storage
Store at RT
Purity
≥98% (HPLC)
Chemical Name
8,8'-[Carbonylbis[imino-3,1-phenylenecarbonylimino(4-methyl-3,1-phenylene)carbonylimino]]bis-1,3,5-naphthalenetrisulfonic acid hexasodium salt
CAS Number
129-46-4
PubChem ID
5360
InChI Key
VAPNKLKDKUDFHK-UHFFFAOYSA-H
SMILES
[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].CC1=CC=C(C=C1NC(=O)C1=CC=CC(NC(=O)NC2=CC=CC(=C2)C(=O)NC2=C(C)C=CC(=C2)C(=O)NC2=C3C(C=C(C=C3S([O-])(=O)=O)S([O-])(=O)=O)=C(C=C2)S([O-])(=O)=O)=C1)C(=O)NC1=C2C(C=C(C=C2S([O-])(=O)=O)S([O-])(=O)=O)=C(C=C1)S([O-])(=O)=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 | |||
| water | 50 | ||
| DMSO | 5 |
Preparing Stock Solutions
for Suramin hexasodium salt
The following data is based on the product molecular weight 1429.15
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 |
|---|---|---|---|
| 0.35 mM | 2.00 mL | 10.00 mL | 19.99 mL |
| 1.75 mM | 0.40 mL | 2.00 mL | 4.00 mL |
| 3.5 mM | 0.20 mL | 1.00 mL | 2.00 mL |
| 17.5 mM | 0.04 mL | 0.20 mL | 0.40 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Luo Suramin is a novel competitive antagonist selective to α1β2γ2 GABAA over ρ1 GABAC receptors. Neuropharmacology. 2018 PMID: 30172846
- Hill Functional regulation of the cardiac ryanodine receptor by suramin and calmodulin involves multiple binding sites. Mol.Pharmacol. 2004 PMID: 15102954
- Voogd Recent research on the biological activity of suramin. Pharmacol.Rev. 1993 PMID: 8396782
- Klinger Suramin and the suramin analogue NF307 discriminate among calmodulin-binding sites. Biochem.J. 2001 PMID: 11311147
- Charlton PPADS and suramin as antagonists at cloned P2Y- and P2U-purinoceptors. Br.J.Pharmacol. 1996 PMID: 8762097
- Beindl Inhibition of receptor/G protein coupling by suramin analogues. Mol.Pharmacol. 1996 PMID: 8700151
Product Specific Notices for Suramin hexasodium salt
For research use only
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