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Cat. No.	Product Name	Target	Signaling Pathways
T23490	UBP310 UBP 310	Others; iGluR	Membrane transporter/Ion channel; Neuroscience; Others
	UBP310 (UBP 310) 是选择性GluR5拮抗剂，Kd 值为 130 nM。
T38659	mGluR5 modulator 1
	mGluR5 modulator 1 is a compound that acts as a positive allosteric modulator of the metabotropic glutamate receptor subtype 5 (mGluR5). Its primary application lies in the field of schizophrenia and cognitive impairment research.
T81801	mGluR5 antagonist-1
	mGluR5 antagonist-1，一种高亲和力的mGluR5拮抗剂，其IC50为11.5 nM，表现出抗抑郁活性。
T27947L	LY339434 HCl LY339434 HCl(219566-62-8 Free base)	GluR; NMDAR	Neuroscience
	LY339434 HCl是一种亲和力很低的GluR5红氨酸受体激动剂。LY339434 HCl 主要通过影响 N-甲基-D-天冬氨酸（NMDA）受体来快速的神经元死亡。
T27949	LY382884 LY-382884,LY 382884	GluR	Neuroscience
	LY382884 是一种具有选择性和有效性的 GLU(K5)受体拮抗剂，具有抗焦虑活性。LY382884可阻断阻断苔藓纤维LTP的诱导。
T0675	Topiramate RWJ 17021,McN 4853,托吡酯	Potassium Channel; Calcium Channel; GABA Receptor; Sodium Channel; GluR; Carbonic Anhydrase; iGluR	Membrane transporter/Ion channel; Metabolism; Neuroscience
	Topiramate (RWJ 17021) 是一种GluR5受体拮抗剂，可通过增强GABAergic 活性，抑制kainate/AMPA 受体，抑制钠和钙通道的电压敏感，增加钾电导并抑制碳酸酐酶来产生抗癫痫作用，用于治疗部分性和全身性癫痫发作。
T10405	ATPA	Others	Others
	ATPA is a selective glutamate receptor GluR5 activator (EC50s: 0.66, 1.4, 9.5, 23, 32, 18, and 14 μM for GluR5wt, GluR5(S721T), GluR5(S741M), GluR5(S721T, S741M), GluR5(S741A), GluR5(S741L), and GluR5(S741V)).
T22546	UBP316 ACET	Others	Others
	GluR5-containing kainate receptor antagonist
T27947	LY339434 LY 339434,LY-339434
	LY339434 is a potent and selective agonist of the kainate receptor GluK1, GluR5.
T13185	Topiramate D12 RWJ 17021 D12,McN 4853 D12	Others	Others
	Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.
T23488	UBP 296	Others	Others
	GluR5-subunit containing kainate receptor antagonist
T61145	Topiramate lithium
	Topiramate lithium (McN 4853) is a wide-ranging antiepileptic compound with GluR5 receptor antagonistic properties. Its mechanism of action involves enhancing GABAergic activity, inhibiting kainate/AMPA receptors, voltage-sensitive sodium and calcium channels, and increasing potassium conductance. Additionally, this compound inhibits carbonic anhydrase. [1][2][3]