
Biological Activity
High affinity 5-HT6 antagonist (Ki = 2.1 nM). Potentiates the hypolocomotor actions of (-)-nicotine in mice.
Technical Data
M. Wt | 448.49 |
Formula | C19H22N2O3S.C2H2O4 |
Storage | Store at +4°C |
Purity | ≥99% (HPLC) |
CAS Number | 275363-58-1 |
PubChem ID | 6918541 |
InChI Key | BLSWAEGCRSFTJG-UHFFFAOYSA-N |
Smiles | O=S(N2C1=CC=C(OC)C=C1C(CCN(C)C)=C2)(C3=CC=CC=C3)=O.OC(C(O)=O)=O |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 22.42 | 50 |
Preparing Stock Solutions
The following data is based on the product molecular weight 448.49. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.23 mL | 11.15 mL | 22.3 mL |
5 mM | 0.45 mL | 2.23 mL | 4.46 mL |
10 mM | 0.22 mL | 1.11 mL | 2.23 mL |
50 mM | 0.04 mL | 0.22 mL | 0.45 mL |
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Product Datasheets
References
References are publications that support the products' biological activity.
Glennon et al (2000) 2-substituted tryptamines: agents with selectivity for 5-HT6 serotonin receptors. J.Med.Chem. 43 1011 PMID: 10715164
Dukat et al (2008) Binding of serotonin and N1-benzenesulfonyltryptamine-related analogs at human 5-HT6 serotonin receptors: receptor modeling studies. J.Med.Chem. 51 603 PMID: 18201064
Nirogi et al (2010) Novel and potent 5-piperazinyl methyl-N1-aryl sulfonyl indole derivatives as 5-HT6 receptor ligands. ACS Med.Chem.Lett. 1 340 PMID:
Young et al (2006) Effect of the 5-HT6 serotonin antagonist MS-245 on the actions of (-)nicotine. Pharmacol.Biochem.Behav. 85 170 PMID: 16950502
Keywords: MS 245 oxalate, supplier, MS245, 5ht6, serotonin, serotonergic, antagonists, 5-HT6, Receptors, 5-HT6, Receptors, Tocris Bioscience