Biological Activity
5-HT2C/2B receptor antagonist, selective over 5-HT1A. Affinities are 7.4 (pA2), 6.9 (pKi) and 5.2 (pKi) for 5-HT2B, 2C and 2A respectively. Orally active in vivo.
Licensing Information
Sold under license
Compound Libraries
SB 200646 hydrochloride is also offered as part of the Tocriscreen Plus. Find out more about compound libraries available from Tocris.
Technical Data
M. Wt | 302.76 |
Formula | C15H14N4O.HCl |
Storage | Store at RT |
Purity | ≥98% (HPLC) |
CAS Number | 143797-62-0 |
PubChem ID | 5311422 |
InChI Key | IGRYPUQJEDJLHC-UHFFFAOYSA-N |
Smiles | Cl.CN1C=CC2=CC(NC(=O)NC3=CN=CC=C3)=CC=C12 |
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 | 30.28 | 100 |
Preparing Stock Solutions
The following data is based on the product molecular weight 302.76. 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 | 3.3 mL | 16.51 mL | 33.03 mL |
5 mM | 0.66 mL | 3.3 mL | 6.61 mL |
10 mM | 0.33 mL | 1.65 mL | 3.3 mL |
50 mM | 0.07 mL | 0.33 mL | 0.66 mL |
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References
References are publications that support the products' biological activity.
Forbes et al (1993) N-(1-Methyl-5-indolyl)-N'-(3-pyridyl)urea hydrochloride: the first selective 5-HT1C receptor antagonist. J.Med.Chem. 36 1104 PMID: 8478907
Kennett et al (1994) In vivo properties of SB 200646A, a 5-HT2C/2B recepor antagonist. Br.J.Pharmacol. 111 797 PMID: 7912626
Kennett et al (1995) Effect of SB 200646A, a 5-HT2C/5-HT2B receptor antagonist, in two conflict models of anxiety. Psychopharmacology (Berl.) 118 178 PMID: 7617805
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