Ondansetron hydrochloride
Tocris Bioscience | Catalog # 2891
Key Product Details
Description
Alternative Names
Product Description
Ondansetron hydrochloride is a selective 5-HT3 receptor antagonist (Ki = 6.16 nM). Also an inhibitor of human multidrug and toxin extrusion (MATE) transporter 1 (IC50 = <10-160 nM). Ondansetron blocks 5-HT-evoked transient inward currents (IC50 = 0.1 nM) in human recombinant h5-HT3A receptors. In an animal model of Parkinson's disease, Ondansetron reduces both the severity of dyskinesia and psychosis-like behaviors. Antiemetic; prevents emesis induced by cytotoxic drugs and radiation.
Product Specifications for Ondansetron hydrochloride
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 | |||
| water | 16.49 | 50 | |
| DMSO | 32.98 | 100 |
Preparing Stock Solutions for Ondansetron hydrochloride
The following data is based on the product molecular weight 329.83.
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 | 3.03 mL | 15.16 mL | 30.32 mL |
| 5 mM | 0.61 mL | 3.03 mL | 6.06 mL |
| 10 mM | 0.30 mL | 1.52 mL | 3.03 mL |
| 50 mM | 0.06 mL | 0.30 mL | 0.61 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 19 publications citing the usage of this product.
- Kwan Selective blockade of the 5-HT3 receptor acutely alleviates dyskinesia and psychosis in the parkinsonian marmoset. Neuropharmacology 2021 PMID: 33152452
- Brown Ion permeation and conduction in a human recombinant 5-HT3 receptor subunit (h5-HT3A). J.Physiol. 1998 PMID: 9508827
- Wittwer Discovery of potent, selective multidrug and toxin extrusion transporter 1 (MATE1, SLC47A1) inhibitors through prescription drug profiling and computational modeling. J.Med.Chem. 2013 PMID: 23241029
- Ginawi Ondansetron, a selective antagonist, antagonizes methamphetamine-induced anorexia in mice. Pharmacol.Res. 2005 PMID: 15661576
- Ye Ondansetron: a selective 5-HT3 receptor antagonist and its applications in CNS-related disorders. CNS Drug Rev. 2001 PMID: 11474424
- Youssefyeh Development of high-affinity 5-HT3 receptor antagonists. 1. Initial structure-activity relationship of novel benzamides. J.Med.Chem. 1992 PMID: 1312602
Product Documents for Ondansetron hydrochloride
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 Ondansetron hydrochloride
For research use only
Citations for Ondansetron hydrochloride
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