JTC-801 hydrochloride
JTC-801
CAS: 244218-51-7
Molecular Formula: C26H25N3O2.ClH
JTC-801 hydrochloride - Names and Identifiers
JTC-801 hydrochloride - Physico-chemical Properties
| Molecular Formula | C26H25N3O2.ClH |
| Molar Mass | 447.963 |
| Melting Point | 235℃ |
| Solubility | DMSO: ≥20mg/mL |
| Appearance | powder |
| Color | tan |
| Storage Condition | Inert atmosphere,2-8°C |
| MDL | MFCD06198707 |
| Use | JTC-801 |
| In vitro study | JTC-801 showed 12.5-,129-, and 1055-fold selectivity for ORL1 receptors (K I = 8.2 nM) over μ-,κ-, and δ-opioid receptors, respectively. In HeLa cells expressing the human ORL1 receptor, JTC-801 did not inhibit Forskolin-stimulated cyclic AMP accumulation, while it prevented the inhibition of pain-sensitive peptide on cyclic AMP accumulation, it shows that JTC-801 has complete antagonistic activity. In the rat cerebral cortex, JTC-801 inhibits the ORL1 receptor with an IC50 of 472 nM and inhibits the μ-receptor with an IC50 of 1831 nM. JTC-801 completely antagonizing the inhibition of Forskolin-induced cyclic AMP accumulation by the pain-sensitive peptide, The IC50 was 2.58 μm in HeLa cells expressing ORL1 receptors. |
| In vivo study | Oral administration of JTC-801 (0.3-3 mg/kg) antagonized the nociceptive hypersensitivity induced by the nociceptide in mice and demonstrated analgesic effects in the electrohotplate test in mice and the formalin test in rats. In the mouse electric hot plate test, the lowest effective dose was 0.01 mg/kg JTC-801 prolonging the escape response latency (ERL) or the thermal stimulus of exposure, I. v. Or 1 mg/kg,p.o. In the rat formalin test, JTC-801 reduced the first and second phase pain responses, MED was 0.01 mg/kg 71, I. v., or 1 mg/kg,p.o. JTC-801 dose-dependent normalization of heat-stimulated paw withdrawal latency (PWL). While JTC-801 did not inhibit chronic compressive nerve injury (CCI)-induced decreases in bone mineral content (BMC) and bone mineral density (BMD), it inhibited the increase in osteoclasts. Tactile pain hypersensitivity induced by L5/L6 spinal nerve ligation was dose-dependently reversed by JTC-801 administration under systemic (3-30 mg/kg) and spinal anesthesia (22.5 and 45 pg). In addition, systemic JTC-801 administration reduced Fos-like immunoreactivity in the spinal cord (slice I/II) gray matter posterior horn. JTC-801 produced a dose-dependent mechanical and complete anti-allodynic effect with ED50 of 0.83 mg/kg and 1.02 mg/kg, respectively. |
JTC-801 hydrochloride - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36 - Irritating to the eyes |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| WGK Germany | 1 |
JTC-801 hydrochloride - Preparation solution concentration reference
| 1mg | 5mg | 10mg | |
|---|---|---|---|
| 1 mM | 2.232 ml | 11.162 ml | 22.323 ml |
| 5 mM | 0.446 ml | 2.232 ml | 4.465 ml |
| 10 mM | 0.223 ml | 1.116 ml | 2.232 ml |
| 5 mM | 0.045 ml | 0.223 ml | 0.446 ml |
Last Update：2024-01-02 23:10:35
JTC-801 hydrochloride - Reference Information
| biological activity | JTC-801 is a selective opiid receptor-like1 (ORL1) receptor (opioid receptor-like 1 receptor) antagonist, the IC50 is 94 nM and weakly inhibits receptors δ, κ and μ. |
| Target | Value |
| Opioid receptor-like1 (ORL1) | 94 nM |
Last Update：2024-04-09 20:49:11
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Mobile: +86-18821248368
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Product Name: JTC-801 Visit Supplier Webpage Request for quotationCAS: 244218-51-7
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tech@medchemexpress.com
Mobile: 609-228-6898
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Product Name: JTC-801 Visit Supplier Webpage Request for quotationCAS: 244218-51-7
Tel: +86-400-900-4166
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Product Name: JTC-801 Visit Supplier Webpage Request for quotation
CAS: 244218-51-7
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Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 244218-51-7
Tel: 18301782025
Email: 3008007409@qq.com
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