Cinitapride Hydrogen Tartrate
Selleck Chemicals
SKU:S5843-5MG
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Cinitapride Hydrogen Tartrate is a modulator of 5-HT Receptors used in studies of GPCR Signaling and Neurotransmission. In practice, this places the compound in experiments that measure receptor-driven second-messenger signaling and desensitization dynamics and synaptic signaling, receptor activity, and neuronal excitability in neuroscience models.
By modulating 5-HT Receptors, Cinitapride Hydrogen Tartrate can be used to examine receptor-driven second-messenger signaling and desensitization dynamics and synaptic signaling, receptor activity, and neuronal excitability. The gpcr annotation adds relevance to GPCR pharmacology, ligand-binding, and signaling assays, together with downstream-response mapping in the same experimental setting. In neuroscience models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.
Research Applications
- Target-focused assays involving 5-HT Receptors
- Pathway perturbation studies connected to GPCR Signaling and Neurotransmission
- Context-dependent response profiling and mechanism comparison
- GPCR pharmacology, ligand-binding, and signaling assays
Overall, Cinitapride Hydrogen Tartrate is appropriate when a defined chemical perturbant is needed to connect 5-HT Receptors with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in neuroscience models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.
- Targets:
- 5-HT Receptors
- Target Class:
- GPCR
- Pathways:
- GPCR Signaling • Neurotransmission
- Research Area:
- Neuroscience
- CAS No.:
- 1207859-16-2
- Molecular Weight:
- 552.57
- Formula:
- C₂₅H₃₆N₄O₁₀
- SMILES:
- CCOC1=CC(=C(C=C1C(=O)NC2CCN(CC2)CC3CCC=CC3)[N+](=O)[O-])N.C(C(C(=O)O)O)(C(=O)O)O
- Storage Temperature:
- -20°C
For Research Use Only. Not intended for diagnostic or therapeutic use.
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