| Size | Price | Stock |
|---|---|---|
| 5mg | $125 | In-stock |
| 10mg | $200 | In-stock |
| 25mg | $400 | In-stock |
| 50mg | $640 | In-stock |
| 100 mg | Get quote | |
| 200 mg | Get quote | |
| We match the lowest price on market. | ||
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| Cat. No. : | HY-106316 |
| M.Wt: | 309.36 |
| Formula: | C18H19N3O2 |
| Purity: | >98 % |
| Solubility: | DMSO : 50 mg/mL (ultrasonic;warming;heat to 60°C) |
CGS 20625 is a potent, selective and orally active partial agonist for the central benzodiazepine receptor. CGS 20625 inhibits [3H]-flunitrazepam binding to central benzodiazepine receptors with an IC50 of 1.3 nM. CGS 20625 enhances GABA in Xenopus laevis oocytes . CGS 20625 can be used for the research of pentylenetetrazol-induced seizures and anxiety[1][2].
IC50 & Target:IC50: 1.3 nM ([3H]-flunitrazepam binding to central benzodiazepine receptors)[1]
In Vitro:CGS 20625 (0.01-100 μM) significantly enhances GABA-induced chloride currents in Xenopus laevis oocytes expressing α1β2γ1 GABAA receptors[2].
CGS 20625 (0.01-100 μM) maximally enhances GABA in Xenopus laevis oocytes expressing α1β2γ2S GABAA receptors with an EC50 of 11.2 μM[2].
CGS 20625 (0.01-100 μM) enhances GABA in Xenopus laevis oocytes expressing α1β2 GABAA receptors, with an EC50[2].
In Vivo:CGS 20625 (p.o.) shows efficacy in preventing pentylenetetrazol-induced seizures (ED50 = 0.7 mg/kg)[1].
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