Chemical Structure : DK-I-56-1
Catalog No.: PC-25017Not For Human Use, Lab Use Only.
DK-I-56-1 is a selective positive allosteric modulator (PAM) of α6 GABAA receptors, enhances GABA-induced chloride flux at α6β3γ2, α6β3δ, or α6β3 receptors at sub-µM or low µM concentrations.
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DK-I-56-1 is a selective positive allosteric modulator (PAM) of α6 GABAA receptors, enhances GABA-induced chloride flux at α6β3γ2, α6β3δ, or α6β3 receptors at sub-µM or low µM concentrations.
DK-I-56-1 is the deuterated version of PZ-II-029.
DK-I-56-1 does not or only weakly modulates GABA-induced currents at αxβ3γ2 GABAA receptors containing α1, α2, α3, α4, or α5 subunits below 1 µM concentration.
DK-I-56-1 inhibited the development and reduced the established trigeminal neuropathic pain in a rat model of chronic constriction injury of the infraorbital branch of the trigeminal nerve.
M.Wt | 324.35 | |
Formula | C18H12D3N3O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Vasović D, et al. Eur J Pain. 2019 May;23(5):973-984.
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