| Name | BTRX-335140 |
| Description | BTRX-335140 (CYM-53093) is a potent and selective orally active κ-opioid receptor (KOR) antagonist with antagonistic activity against κOR, μOR, and δOR with IC50 values of 0.8, 110, and 6500 nM, respectively. |
| In vitro | METHODS: Tango OPRK1-bla U2OS cells were used to express KORs associated with the GAL4-VP16 transcription factor through the TEV protease locus.
RESULTS Navacaprant (BTRX-335140) showed antagonistic activity against κOR, μOR and δOR with IC50 values of 0.8 nM, 110 nM and 6.5 μM, respectively.[1] |
| In vivo | METHODS: Mice were injected with BTRX-335140 (CYM-53093) (1 mg/kg, i.p.) 1 h and 24 h prior to the injection of U-50488 (15 mg/kg, i.v.) and tail-wagging latencies were measured at baseline, 30 min and 60 min after the agonist injection, while the mice were administered BTRX-335140 (CYM-53093) (3, 10, and 30 mg/kg) (3, 10, and 30 mg/kg) orally alone. 53093) (3, 10, and 30 mg/kg) alone, while mice were orally administered BTRX-335140 (CYM-53093) to assess the ability of BTRX-335140 (CYM-53093) to antagonize the antinociceptive effects of U-50488.
RESULTS BTRX-335140 (CYM-53093) (1 mg/kg, i.p.) blocked U-50488-induced antinociception within 1 h. The delayed tail-flash response induced by oral administration of BTRX-335140 (CYM-53093) (1 mg/kg) alone did not show any significant change in the tail-flash response induced by oral BTRX-335140 (CYM-53093) (1 mg/kg) at 1 h post-dosing in rats. 335140 (CYM-53093) (3, 10 and 30 mg/kg) also blocked U-50488-induced antinociception in a dose-dependent manner. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | DMSO : 5.5 mg/mL (12.13 mM), Sonication is recommended.
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| Keywords | BTRX335140 | CNS | CYM53093 | U69593 | BTRX 335140 | Inhibitor | U2OS | Opioid Receptor | inhibit | neurobehavioral disorder | BTRX-335140 | CYM 53093 | oral |
| Inhibitors Related | Docusate sodium | Bevenopran | Mirtazapine | Sinomenine | (-)-Menthol | Matrine | SCH 221510 | Progesterone | Naltrexone hydrochloride | Trimebutine | Mianserin hydrochloride | Amentoflavone |
| Related Compound Libraries | Anti-Neurodegenerative Disease Compound Library | Bioactive Compound Library | Pain-Related Compound Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Bioactive Compounds Library Max | GPCR Compound Library | Anti-Cancer Drug Library |
United States
