Neuroscience(神经科学)

Neuroscience
Neurons communicate with each other, effector organs and sensory organs through the neurotransmitter – receptor pathway at synapses. Neurotransmitters can be divided into 4 major groups: 1. Amino acids (glumate, aspartate, serine, glycine and GABA); 2. Monoamines (norepinephrine, epinephrine, dopamine, histamine, and serotonin); 3. Peptides (opioid peptides, substance P, somatostatin); and 4. Others (acetylcholine, NO, nucleosides). read more
Products for Neuroscience
- 5-HT Receptor(420)
- AChR(53)
- AChE(100)
- Alzheimer(107)
- Amyloid β(118)
- BACE(4)
- CGRP (33)
- COX(294)
- DAPK(7)
- Dopamine Receptor(290)
- GABA Receptor(155)
- Gap Junction(16)
- GluR(116)
- Histamine(2)
- Histamine Receptor(236)
- mPEGS-1(4)
- Muscarinic Receptor(41)
- Neuroscience Peptides(38)
- Nicotinic Receptor(62)
- P2 Receptor(2)
- P2X7 receptor(3)
- SSRIs(5)
- Substance P/NK1 Receptor(20)
- NMDA(2)
- Beta-secretase(25)
- CaMK(32)
- Dopamine Transporter(20)
- Monoamine Oxidase(91)
- Serotonin Transporter(57)
- nAChR(100)
- iGluR(155)
- Neurokinin Receptor(75)
- MCHR1 (GPR24)(16)
- mAChR(183)
- GPR139(4)
- Cholecystokinin Receptor(25)
- Behavioral Neuroscience(353)
- DREADD(1)
- Huntington(14)
- Neuroendocrinology(64)
- Neuroprotection(117)
- Ophthalmology(158)
- Pain Research(229)
- Parkinson(73)
- Prion(7)
- Seizure Disorders(94)
- Cholinesterases(13)
- Tau Protein(4)
- Neurodegenerative Disorders(5)
- Cholinesterase (ChE)(3)
- Amyloid-β(9)
- γ-secretase(1)
- Ischemia(3)
- Cat.No. 产品名称 Information
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GC48232
Valdecoxib-d3
戊地昔布-D3,SC 65872-d3
An internal standard for the quantification of valdecoxib -
GC10335
Valeroyl Salicylate
戊酰基水杨酸,2-Valeryloxybenzoic Acid
A selective, irreversible inhibitor of COX-1 -
GC41613
Valnoctamide
戊诺酰胺,Valmethamide
An anxiolytic that suppresses seizures -
GC45137
Valproic Acid Acyl-D-Glucuronide
Valproic Acid Gluclonide
A metabolite of valproic acid -
GC13322
Vanoxerine
GBR 12909; I893
Vanoxerine (GBR-12909) 是一种竞争性、强效和高度选择性的多巴胺再摄取抑制剂 (Ki=1 nM)。 -
GC17741
Vanoxerine dihydrochloride
伐诺司林二盐酸盐,GBR-12909 dihydrochloride; I893 dihydrochloride
An inhibitor of dopamine uptake -
GC45139
Vapreotide (trifluoroacetate salt)
BMY 41606, Octastatin, RC 160
A peptide NK1 receptor antagonist -
GC12762
Varenicline
伐尼克兰; CP 526555
Varenicline (CP 526555) 是一种有效的 α4β2 烟碱乙酰胆碱受体 (nAChR) 部分激动剂,EC50 值为 2.3 μM。 -
GC26032
Varenicline (CP 526555) dihydrochloride
Chantix, Champix,CP 526555 dihydrochloride
Varenicline (CP 526555, Chantix, Champix,CP 526555 dihydrochloride) dihydrochloride is a potent, partial agonist of α4β2 nicotinic acetylcholine receptor (nAChR) and α3β4 nAChR with EC50 of 2.3 μM and 55 μM, respectively. Varenicline dihydrochloride is a potent, full agonist of α7 nAChRs with EC50 of 18 μM. Varenicline is a prescription medication used for smoking cessation. -
GC16143
Varenicline Hydrochloride
6,7,8,9-四氢-6,10-甲桥-6H-吡嗪并[2,3-H][3]苯并氮杂卓盐酸盐,CP 526555 hydrochloride
Varenicline Hydrochloride (CP 526555 hydrochloride) 是一种高亲和力、选择性的 α4β2 尼古丁乙酰胆碱受体 (nAChR) 部分激动剂和完整的 α7 nAChR 激动剂。 -
GC10948
Varenicline Tartrate
酒石酸伐尼克兰; CP 526555-18
Varenicline Tartrate是一种选择性α7和α4β2烟碱型乙酰胆碱受体(nAChR)激动剂,对α4β2 nAChR的IC50值为250nM。 -
GC48244
Varenicline-d4
伐尼克兰-D4,CP 526555-d4
An internal standard for the quantification of varenicline -
GC62199
Vazegepant hydrochloride
Zavegepant hydrochloride; BHV-3500 hydrochloride
Vazegepant (BHV-3500) hydrochloride 是一种高度亲和性 CGRP 受体拮抗剂 (hCGRP Ki=0.023 nM)。Vazegepant hydrochloride 是第一种用于偏头痛的鼻用 gepant。Vazegepant hydrochloride 可能有助于有效管理 COVID-19 相关肺部炎症。 -
GC11210
Vecuronium Bromide
维库溴铵; ORG NC 45
Vecuronium Bromide是一种非去极化神经肌肉阻断剂,特异性地作用于肌肉型乙酰胆碱受体,IC50为1-2nM。 -
GC63427
Velufenacin
Velufenacin 是毒蕈碱型受体 (muscarinic receptor) 的拮抗剂。
-
GC63251
Velusetrag
1,2-二氢-N-[(3-内)-8-[(2R)-2-羟基-3-[甲基(甲磺酰基)氨基]丙基]-8-氮杂双环[3.2.1]辛-3-基]-1-(1-甲基乙基)-2-氧代-3-喹啉甲酰胺,TD-5108
Velusetrag (TD-5108) 是一种具有口服活性,有效和选择性的血清素 5-HT4 受体 (5-HT4R) 激动剂,pKi 为 7.7。Velusetrag 对 5-HT2A 和 5-HT2B 受体没有亲和力 (Ki>10 μM)。Velusetrag 可用于胃肠道疾病和帕金森病的研究。 -
GC63252
Velusetrag hydrochloride
TD-5108 hydrochloride
Velusetrag (TD-5108) hydrochloride 是一种具有口服活性,有效和选择性的血清素 5-HT4 受体 (5-HT4R) 激动剂,pKi 为 7.7。Velusetrag hydrochloride 对 5-HT2A 和 5-HT2B 受体没有亲和力 (Ki>10 μM)。Velusetrag hydrochloride 可用于胃肠道疾病和帕金森病的研究。 -
GC10911
Venlafaxine hydrochloride
盐酸文拉法辛; Wy 45030 hydrochloride
An Analytical Reference Material -
GC71620
Venlafaxine-d6
Venlafaxine-d6是氘标记的文拉法辛。
-
GC30824
Veralipride ((±)-Veralipride)
维拉必利,(±)-Veralipride; LIR166
Veralipride ((±)-Veralipride) 是一种 D2 受体拮抗剂。
-
GC61371
Veratric acid
藜芦酸
Veratricacid(3,4-Dimethoxybenzoicacid)是从蔬菜和水果中得到的多酚物质,可口服,具有抗氧化、保护心血管和抗炎活性。当细胞受到UVB辐射时,Veratricacid能够减少上调的COX-2表达,降低PGE2和IL-6水平。 -
GC33632
Veratric acid (3,4-Dimethoxybenzoic acid)
藜芦酸; 3,4-Dimethoxybenzoic acid
Veratric acid (3,4-Dimethoxybenzoic acid), a simple benzoic acid derived from plants and fruits, has anti-oxidant, anti-inflammation, and blood pressure-lowering effects. Veratric acid reduces upregulated COX-2 expression, and levels of PGE2, IL-6 after UVB irradiation. -
GC11098
Verubecestat (MK-8931)
维罗司他; MK-8931
An inhibitor of BACE1 and BACE2 -
GC26035
Verubecestat (MK-8931) Trifluoroacetate
MK-8931
Verubecestat (MK-8931) Trifluoroacetate is a potent and selective beta-secretase inhibitor and BACE1 protein inhibitor or Beta-site APP-cleaving enzyme 1 inhibitor. -
GC37905
Vigabatrin
氨己烯酸; γ-Vinyl-GABA
Vigabatrin是 γ-氨基丁酸转氨酶 (GABA-T) 的不可逆抑制剂,具有提高脑 GABA 水平和增强抑制性神经传递的强效活性。 -
GC13387
Vigabatrin Hydrochloride
盐酸氨己烯酸; γ-Vinyl-GABA hydrochloride
Inhibitor of GABA transaminase -
GC48248
Vigabatrin-13C-d2 (hydrochloride)
γ-Vinyl-GABA-13C,d2 hydrochloride
A neuropeptide with diverse biological activities -
GC15013
Vilazodone
维拉佐酮; EMD 68843; SB659746A
Vilazodone (EMD 68843; SB 659746A) 是一种强效、选择性和口服活性的血清素再摄取抑制剂 (SSRI) 和部分 5-HT1A 受体激动剂。 -
GC37906
Vilazodone D8
盐酸维拉佐酮 d8
An internal standard for the quantification of vilazodone -
GC10876
Vilazodone Hydrochloride
盐酸维拉佐酮; EMD 68843 Hydrochloride; SB659746A Hydrochloride
An SSRI and a partial agonist of 5-HT1A -
GC31262
Vinconate (Chanodesethylapovinc amine)
长春考酯,Chanodesethylapovinc?amine
Vinconate (Chanodesethylapovinc amine) 是一种吲哚萘啶衍生物,可刺激毒蕈碱乙酰胆碱受体。 -
GC38026
Violanthin
紫罗兰素
Violanthin 是从胡椒 Piper bavinum 中分离出来,具有抗氧化和抗菌活性。Violanthin 抑制乙酰胆碱酯酶 (AChE),IC50 值为 79.80 μM。 -
GC45146
VIP (human, porcine, rat, ovine) (trifluoroacetate salt)
Vasoactive Intestinal Peptide
A peptide with diverse biological activities -
GC49168
Visnagin
齿阿米素
A furanochromone with diverse biological activities -
GC48253
Vitamin B12 (hydrate)
Cobalamin
A neuropeptide with diverse biological activities -
GC33747
Vofopitant (GR 205171)
GR 205171
Vofopitant (GR 205171) 是有效的速激肽 NK1 受体拮抗剂,对人、大鼠和雪貂 NK1 受体的 pKis 分别为 10.6、9.5 和 9.8。 -
GC37918
Vofopitant dihydrochloride
GR 205171A
Vofopitant dihydrochloride (GR 205171A) 是一种有效、选择性的,口服有效的速激肽 NK1 受体拮抗剂,在大鼠和人类细胞膜上抑制 [3H]SP 与 NK1 结合的 pKi 值分别为 9.5 和 10.6,具有成为广谱的止吐剂的潜力。 -
GC71085
Volinanserin-d4 hydrochloride
Volinanserin-d4 hydrochloride是氘标记的Volinanserin盐酸盐。
-
GC60383
Vomifoliol
吐叶醇
Vomifoliol是一种与脱落酸(ABA)有关的化合物,具有修饰的2,4-戊二烯侧链,其活性与ABA的活性相当。Vomifoliol表现出抗乙酰胆碱酯酶(antiacetylcholinesterase)活性和中等抗利什曼虫(antileishmanial)活性。 -
GC16312
Vortioxetine
沃替西汀; Lu AA 21004
A multimodal serotonergic agent -
GC14437
Vortioxetine (Lu AA21004) HBr
盐酸沃替西汀; Lu AA21004 hydrobromide
A multimodal serotonergic agent -
GC48255
Vortioxetine-d8
Lu AA 21004 D8
An internal standard for the quantification of vortioxetine -
GC70130
VQW-765
AQW-051
VQW-765 (AQW-051) 是一种选择性的、具有口服活性的 alpha-7 烟碱乙酰胆碱受体 (α7-nAChR) 激动剂,对重组表达的人 α7-nAChR 的 pKD 值为 7.56。VQW-765 在体内表现出抗焦虑作用。VQW-765 可用于焦虑障碍和急性焦虑的研究。 -
GC15198
VU 0155041
A selective positive allosteric modulator of mGluR4
-
GC14003
VU 0155041 sodium salt
A selective positive allosteric modulator of mGluR4
-
GC15990
VU 0238429
HY-12157, ML129
A muscarinic M5 receptor positive allosteric modulator -
GC10464
VU 0255035
N-(3-氧代-3-(4-(吡啶-4-基)哌嗪-1-基)丙基)苯并[C][1,2,5]噻二唑-4-磺酰胺,VU 255035
A selective muscarinic M1 receptor antagonist -
GC16643
VU 0285683
negative allosteric modulator of mGlu5 receptors
-
GC16655
VU 0357017 hydrochloride
CID-25010775
An M1 muscarinic acetylcholine receptor agonist -
GC10323
VU 0360172 hydrochloride
A positive allosteric modulator of mGluR5