Tropisetron HCL (5-HT3 Receptor Antagonist) Research Standard
Tropisetron HCL is a synthetic indole derivative featuring a tropane ring structure, widely utilized in laboratory research as a potent and selective 5-HT3 receptor antagonist. By blocking the 5-HT3 receptor, the compound serves as a vital chemical probe for studying serotonergic signaling pathways. In controlled in vitro models, researchers leverage its structural profile—featuring both an indole ring system and a tropane nitrogen—to explore receptor-binding kinetics, competition dynamics, and the physiological consequences of inhibiting 5-HT3 receptor activation.
Technical Specifications
| Property | Specification |
| Product Name | Tropisetron HCL |
| Chemical Formula | C17H20N2O2•HCl |
| Molecular Weight | 320.8 g/mol |
| Chemical Class | 5-HT3 Receptor Antagonist / Indole derivative |
| Physical Appearance | Off Pink Crystalline |
| Assay Purity | ≥ 98% (HPLC verified) |
Mechanism of Action & Research Context
Tropisetron HCL is primarily studied for its pharmacological activity as a serotonin (5-HT3) receptor antagonist.
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5-HT3 Antagonism: The compound acts by competitively binding to the 5-HT3 receptor, thereby inhibiting the activation of this ligand-gated ion channel. Research focuses on the impact of this inhibition on ion flux and downstream serotonergic signaling.
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Structural Interaction: Its indole moiety participates in π-π stacking interactions, while the tropane nitrogen provides ionic stabilization, allowing the molecule to lock into the receptor’s binding site effectively.
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Signaling Pathways: Scientists use Tropisetron HCL to investigate 5-HT3 receptor-mediated pathways in cell-free and cell-based assay systems, contributing to a broader understanding of serotonergic modulation in neurological and physiological research.
Research Applications
Tropisetron HCL is a specialized reagent essential for molecular signaling and neuropharmacological research.
Primary fields of in vitro laboratory investigation include:
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Receptor-Binding Dynamics: Measuring the affinity and occupancy of the compound at 5-HT3 receptor sites.
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Serotonergic Signaling: Evaluating the physiological effects of inhibiting 5-HT3 receptor-mediated neurotransmission in isolated neural preparations.
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Competition Assays: Investigating how the compound competes with serotonin and other agonists for 5-HT3 receptor sites.
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Structure-Activity Analysis: Mapping the specific molecular requirements of the indole/tropane scaffold for antagonist efficacy.
Storage & Handling Guidelines
To maintain the chemical stability and experimental reliability of the compound, please note the format-specific requirements:
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Light Protection: Protect all formats from direct light exposure to prevent degradation.
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Container Integrity: Ensure containers remain tightly sealed to prevent moisture ingress.
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Aseptic Technique: Utilize only sterile, non-reactive laboratory tools to prevent cross-contamination during sampling.
Research Use Disclaimer
Research Use Only Disclaimer: This product is developed and distributed strictly as a Research Use Only (RUO) laboratory reference chemical intended exclusively for non-clinical analytical and scientific investigation. It is not an FDA-approved drug, medical treatment, dietary supplement, or food ingredient, and is strictly prohibited for human or animal consumption. Kimera Chems supplies this high-purity research material solely to qualified institutions and professional investigators for authorized laboratory research.
| CAS Number | 105826-92-4 |
| Other Names | Tropisetron, Tropisetron HCl, Tropisetron Hydrochloride, ICS 205-930, SDZ-ICS 930 |
| IUPAC Name | 1H-indole-3-carboxylic acid (3-endo)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, monohydrochloride |
| Molecular Formula | C₁₇H₂₀N₂O₂•HCl |
| Molecular Weight | 320.8 |
| Liquid Concentration And Solution | 20mg Per mL Acetate Buffered Deionized Water |




