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Cat. No.	Product Name	Target	Signaling Pathways
T3470	Cis-ACBD cis-1-aminocyclobutane-1,3-dicarboxylic acid,氨基二羧酸	Amino Acids and Derivatives	Metabolism
	Cis-ACBD (cis-1-aminocyclobutane-1,3-dicarboxylic acid) 是一种有效的选择性 N-甲基-D-天冬氨酸受体激动剂。
T0313	Evans blue Direct Blue 53,C.I. 23860,伊文思蓝	GluR	Neuroscience
	Evans blue (C.I. 23860) 是一种突触泡谷氨酸吸收的有效抑制剂，同时也是一种AMPA/kainate 受体拮抗剂。
T13536	Afoxolaner	Chloride channel; GABA Receptor; Parasite	Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience
	Afoxolaner 是一种异恶唑啉杀虫剂/杀螨剂，可对抗犬的肩胛硬蜱。它作用于昆虫的 γ-氨基丁酸(GABA)受体谷氨酸受体，抑制 GABA 和谷氨酸调节的氯离子吸收，导致过度的神经元刺激和节肢动物死亡。
T22043	BCATc Inhibitor 2	Others	Others
	BCATc Inhibitor 2 是选择性分支链氨基转移酶抑制剂，可用于神经退行性疾病的研究。能够抑制 rBCATc (IC50:0.2 μM)，hBCATc (IC50:0.8 μM)、 rBCATm (IC50:3.0 μM)。其中BCATc 也称为 BCAT1，存在于细胞质基质中的亚型。
T0267	Zonisamide AD 810,唑尼沙胺,CI 912	Calcium Channel; Sodium Channel; Carbonic Anhydrase	Membrane transporter/Ion channel; Metabolism
	Zonisamide (AD 810) 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂，对人类线粒体同工酶 hCA II 和 hCA V 作用的 Ki 值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性，在癫痫、癫痫发作和帕金森病的研究中具有价值。
T22913	L-CCG-lll	Others	Others
	inhibitor of both glial and neuronal uptake of glutamate, aspartate and cysteate.
T29153	WAY-855
	WAY-855 is an EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptake.
T22722	Dihydrokainic acid	Others	Others
	EAAT2(GLT1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake
T11055	DL-TBOA	transporter	Metabolism
	DL-TBOA inhibited [14C] glutamate uptake in COS-1 cells expressing human EAAT1 and EAAT2, with Ki values of 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner, with Ki values of 4.4 μM and 3.2 μM, respectively. DL-TBOA
T39510	DL-TBOA ammonium
	DL-TBOA ammonium is a potent, non-transportable inhibitor of excitatory amino acid transporters. Its inhibitory effects are demonstrated by IC50 values of 70 μM, 6 μM, and 6 μM for excitatory amino acid transporter-1 (EAAT1), EAAT2, and EAAT3, respectively. Additionally, DL-TBOA ammonium significantly hampers the uptake of [14C]glutamate in COS-1 cell lines expressing human EAAT1 and EAAT2, evident by Ki values of 42 μM and 5.7 μM, respectively. Furthermore, this compound competitively blocks EA...