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19

抑制剂 & 化合物

3

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T8458	CNQX disodium	iGluR	Membrane transporter/Ion channel; Neuroscience
	CNQX disodium 是一种有效的、竞争性的 AMPA /海藻酸酯受体 (AMPA/kainate receptor) 拮抗剂，IC50分别为 0.3 μM 和 1.5 μM。它能够阻止大鼠恐惧增强的表达，是一种竞争性的非 NMDA 受体拮抗剂。
T8459	DNQX disodium salt DNQX Disodium	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	DNQX disodium salt 是一种选择性、强竞争性的非 NMDA 谷氨酸受体 (non-NMDA glutamate receptor) 拮抗剂 (对 AMPA、kainate 和 NMDA 受体的 IC50分别为 0.5、2 和 40 μM)，是一种喹恶啉衍生物。
T7304	DNQX 二硝基喹酮,FG 9041	GluR; iGluR	Membrane transporter/Ion channel; Neuroscience
	DNQX (FG 9041) 是喹恶啉衍生物，是一种选择性和强竞争性的非 NMDA 谷氨酸受体拮抗剂，对 AMPA、kainate 和 NMDA 受体的IC50分别为 0.5、2 和 40 μM。
T7178	CNQX FG9065,6-氰基-7-硝基喹喔啉-2,3-二酮	GluR; iGluR	Membrane transporter/Ion channel; Neuroscience
	CNQX (FG9065) 是一种竞争性、非 NMDA 谷氨酸受体拮抗剂，对 AMPA 和红藻氨酸受体的IC50分别为 0.3 和 1.5 μM。
T2362	QNZ46	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	QNZ46 是一种 NR2C/NR2D 选择性 NMDA 受体非竞争性拮抗剂。
T26645	Aptiganel CNS 1102,CNS-1102,CNS1102	NMDAR	Neuroscience
	Aptiganel (CNS-1102) 是一种非竞争性 NMDA 拮抗剂，是一种多肽，可用于研究急性缺血性卒中。
T23048	N20C hydrochloride 盐酸N20C,2-((3,3-diphenylpropyl)amino)acetamide hydrochloride	NMDAR	Neuroscience
	N20C hydrochloride (2-((3,3-diphenylpropyl)amino)acetamide hydrochloride) 是一种非竞争性 NMDA 受体开放通道阻滞剂。
T22798	Gavestinel GV 150526,Gavestinel sodium salt	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	Gavestinel (GV 150526) 是一种非竞争性的 NMDA 受体拮抗剂，具有有效性、选择性和口服活性。Gavestinel 可与 NMDA 受体的甘氨酸位点结合，其结合亲和力(pKi 值)为 8.5。Gavestinel 可用于急性缺血性脑卒中研究。
T6352	(-)-Dizocilpine maleate C13737,(-)-MK 801 (Maleate),(-)-MK 801马来酸,(-)-MK 801 Maleate	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	(-)-Dizocilpine maleate ((-)-MK 801 (Maleate)) 是一种选择性且非竞争性的 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂，Ki 为 211.7 nM。它是一种 Dizocilpine 的活性较低的 (-)-对映体，具有抗抑郁作用。
T1751	Eliprodil 依利罗地,SL-820715	NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	Eliprodil (SL-820715) 是NR2B-NMDA 受体高效选择性抑制剂，IC50值1uM。它对NR2A-和NR2C-NMDA 受体作用较弱，可用于研究帕金森病和运动障碍治疗的试验。
T22513	4-PPBP maleate	Sigma receptor; NMDAR	GPCR/G Protein; Neuroscience
	4-PPBP maleate 是一种有效的 σ1 受体（配体）激动剂。4-PPBP maleate 在Xenopus oocytes 表达的情况下可被认为是一种具有选择性、非竞争性的 NR1a/2B NMDA 受体拮抗剂。4-PPBP maleate 具有神经保护特性。
T6504	Flupirtine maleate Katadolon maleate,氟吡啶马来酸,马来酸氟吡汀	Potassium Channel; NMDAR; iGluR	Membrane transporter/Ion channel; Neuroscience
	Flupirtine maleate (Katadolon maleate) 是可透过血脑屏障的、具有口服活性的非阿片类化合物。它是间接 NMDAR 拮抗剂，可用于缓解疼痛的研究，具有神经保护特性。
T22640	CCMQ	Others	Others
	inhibits [3H]-homoquinolinic acid binding to non-NMDA sensitive sites
TP2235	Conantokin-T	Others	Others
	Non-competitive NMDA receptor antagonist
T61470	NMDA receptor antagonist 5
	NMDA receptor antagonist 5 (Compound 10e), a potent and non-toxic NMDA receptor antagonist, exhibits brain permeability. It is of significance in studying neurological disorders [1].
T11522	GYKI 52466 dihydrochloride	Others	Others
	GYKI 52466 dihydrochloride is orally active and non-competitive kainate- and AMPA-activated currents antagonist (IC50s: 7.5 μM and 11 μM). It is inactive against NMDA or γ-aminobutyric acid responses. It is a muscle relaxant and anticonvulsant agent and h
T21449	GYKI-52466 GYKI 52,466,GYKI-5,2466,GYKI52,466
	GYKI-52466 is a selective non-competitive AMPA receptor antagonist (IC50 values are 10-20, ~ 450 and >50 μM for AMPA-, kainate- and NMDA-induced responses, respectively) used as a Skeletal muscle relaxant, orally active anticonvulsant, neuroprotective and
T69422	Flupirtine HCl
	Flupirtine HCl is the salt form of Flupirtine, also known as W-2964, an aminopyridine that functions as a centrally acting non-opioid analgesic. It first became available in Europe in 1984, and is sold mainly under the names Katadolon, Trancolong, Awegal, Efiret, Trancopal Dolo, and Metanor. Like nefopam, it is unique among analgesics in that it is a non-opioid, non-NSAID, non-steroidal centrally acting analgesic. Flupirtine is a selective neuronal potassium channel opener that also has NMDA re...
T37671	CAY10608 CAY10608
	N-Methyl-D-aspartate (NMDA) receptors are Ca2+ permeable ligand-gated channels of the central nervous system that are activated after binding of the co-agonists glutamate and glycine. CAY10608 is a propanolamine that potently, selectively, and non-competitively antagonizes the NR2B subunit of NMDA receptors (IC50 = 50 nM). It does not inhibit NR1, NR2A, NR2C, and NR2D subunits and has no significant effects on α-amino-3-hydroxy-5-methyl-4-isoxazolepropioinic acid (AMPA) or kainate receptors. CAY...

化合物

Cat.No: T8458

Target: iGluR

DNQX disodium salt

Cat.No: T8459

Synonym: DNQX Disodium

Target: NMDAR, iGluR

Cat.No: T7304

Synonym: 二硝基喹酮,FG 9041

Target: GluR, iGluR

Cat.No: T7178

Synonym: FG9065,6-氰基-7-硝基喹喔啉-2,3-二酮

Target: GluR, iGluR

Cat.No: T2362

Target: NMDAR, iGluR

Cat.No: T26645

Synonym: CNS 1102,CNS-1102,CNS1102

Target: NMDAR

N20C hydrochloride

Cat.No: T23048

Synonym: 盐酸N20C,2-((3,3-diphenylpropyl)amino)acetamide hydrochloride

Target: NMDAR

Cat.No: T22798

Synonym: GV 150526,Gavestinel sodium salt

Target: NMDAR, iGluR

(-)-Dizocilpine maleate

Cat.No: T6352

Synonym: C13737,(-)-MK 801 (Maleate),(-)-MK 801马来酸,(-)-MK 801 Maleate

Target: NMDAR, iGluR

Cat.No: T1751

Synonym: 依利罗地,SL-820715

Target: NMDAR, iGluR

Cat.No: T22513

Target: Sigma receptor, NMDAR

Flupirtine maleate

Cat.No: T6504

Synonym: Katadolon maleate,氟吡啶马来酸,马来酸氟吡汀

Target: Potassium Channel, NMDAR, iGluR

Cat.No: T22640

Target: Others

Cat.No: TP2235

Target: Others

NMDA receptor antagonist 5

Cat.No: T61470

GYKI 52466 dihydrochloride

Cat.No: T11522

Target: Others

Cat.No: T21449

Synonym: GYKI 52,466,GYKI-5,2466,GYKI52,466

Cat.No: T69422

Cat.No: T37671

Synonym: CAY10608

Cat. No.	Product Name	Target	Signaling Pathways
T3377	L-Phenylalanine L-苯丙氨酸,(S)-2-Amino-3-phenylpropionic acid,phenylalanine,3-Phenyl-L-alanine	Calcium Channel; Endogenous Metabolite; iGluR	Membrane transporter/Ion channel; Metabolism; Neuroscience
	L-Phenylalanine (3-Phenyl-L-alanine) 是分离自大肠杆菌的必需氨基酸，是 NMDARs(KB573 μM) 和非 NMDARs 的甘氨酸和谷氨酸结合位点的竞争性拮抗剂，用于食品香料和药品的生产中。它是一种电压依赖性 α2δ 亚基 Ca2+通道拮抗剂，Ki 为 980 nM。
T6S0659	Rhynchophylline 钩藤碱,Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin	Calcium Channel; NF-κB	Membrane transporter/Ion channel; Metabolism; NF-κB
	Rhynchophylline (Mitrinermine) 是一种生物碱类化合物，从钩藤中分离得到，具有很高的生物活性，被广泛用于抗炎、神经保护等方面的研究。
T2O2728	glycine 2-Aminoacetic acid,Glycolixir,Aminoacetic acid,Glycosthene,Glycocoll,甘氨酸	MT Receptor; Endogenous Metabolite; iGluR	Membrane transporter/Ion channel; Metabolism; Neuroscience
	glycine (2-Aminoacetic acid) 是中枢神经系统的抑制性神经递质，也是谷氨酸的联合激动剂，有促进谷氨酸能NMDA 受体兴奋的潜力。它主要存在于明胶和丝素蛋白中，并在治疗上用作营养物质。

天然产物

L-Phenylalanine

Cat.No: T3377

Synonym: L-苯丙氨酸,(S)-2-Amino-3-phenylpropionic acid,phenylalanine,3-Phenyl-L-alanine

Target: Calcium Channel, Endogenous Metabolite, iGluR

Rhynchophylline

Cat.No: T6S0659

Synonym: 钩藤碱,Rhynchophyllin,Rhyncophylline,Mitrinermine,Mitrinermin

Target: Calcium Channel, NF-κB

Cat.No: T2O2728

Synonym: 2-Aminoacetic acid,Glycolixir,Aminoacetic acid,Glycosthene,Glycocoll,甘氨酸

Target: MT Receptor, Endogenous Metabolite, iGluR

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