"目錄號(hào): HY-14417A
(1R,2S)-VU0155041是VU0155041的順式異構(gòu)體蜘拉。(1R,2S)-VU0155041是mGluR4的部分激動(dòng)劑，EC50值為2.35 μM锄弱。
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生物活性
Description
(1R,2S)-VU0155041,Cisregioisomer of VU0155041, is a partialmGluR4agonist with anEC50of 2.35 μM.
IC50& Target
EC50: 2.35 μM (rat mGluR4)[1]
In Vitro
At both human and rat receptors, theCisregioisomer of VU0155041 is similar in potency (798±58 nM at human mGluR4 and 693±140 nM at rat mGluR4). Conversely, the concentration-response curve for theTransregioisomer (VU0155040) does not plateau at the maximum concentration tested. Fold-shift experiments at 30 μM of VU0155041 also shows that theCisregioisomer is more effective at this concentration on both human and rat mGluR4. VU0155041, induces concentration-dependent shifts in the baseline when examined in fold shift experiments using the thallium flux assay. VU0155041 induces a response that reaches approximately 45% of the maximal glutamate response. VU0155041is a partial agonist of mGluR4 that activates the receptor by interacting with a site that is distinct from the glutamate binding site. VU0155041 exhibitsselectivity for mGluR4 relative to 67 different targets and does not affect the function of striatal NMDA receptors[1].
In Vivo
VU0155041 is soluble in an aqueous vehicle and intracerebroventricular administration of 31 to 316 nM of VU0155041 dose-dependently decreases haloperidol-induced catalepsy and reserpine-induced akinesia in rats. VU0155041, at doses of 31 and 92 nmol, is also able to significantly decrease the cataleptic effects of haloperidol, and the effects of the compound are still present 30 min after infusion. Icv infusion of a 316 nmol dose of VU0155041 also results in a significant reversal of akinesia[1].
References
