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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GC38198
Revaprazan hydrochloride
盐酸瑞伐拉赞
Revaprazan Hydrochloride (YH1885) is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. Revaprazan Hydrochloride reversibly inhibits H(+)/K(+)-ATPase via binding to the K+-binding site of the pump. -
GC31761
Revefenacin (TD-4208)
雷芬那辛,TD-4208; GSK1160724
Revefenacin (TD-4208, GSK-1160724) is a potent, lung-selective, long-acting muscarinic antagonist that may be for the treatment of respiratory disease. -
GC30681
Revexepride
Revexepride是一种高度选择性的5-HT4receptor激动剂,也是潜在的CYP3A4enzyme诱导剂,可用于治疗胃食管返流疾病。
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GC34158
RG-12915
RG-12915是一种选择性的5-HT3拮抗剂,IC50值为0.16nM。
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GC12411
RHC 80267
1,6-双(环己基脒基羰基氨基)己烷,U-57908
An inhibitor of DAGL -
GC45798
Rhein-13C4
1,8-二羟基-3-羧基蒽醌
An internal standard for the quantification of rhein
-
GC91920
Rhein-13C6
Rheic Acid-13C6
Rhein-13C6旨在用作GC或LC-MS定量大黄酸的内标。 -
GC44833
Rhodamine B isothiocyanate (mixed isomers)
RBITC, RITC
A fluorogenic dye -
GN10145
Rhodionin
草质素苷
Rhodionin 是从 Rhodiola crenulata 的根中分离出来的,是一种特异性的非竞争性细胞色素 P450 2D6 抑制剂,IC50 为 0.761 μM,Ki 为 0.769 μM。 -
GC37528
Rhodiosin
红景天素
Rhodiosin 是从红景天 (Rhodiola crenulata) 的根中分离的,一种特异性非竞争性细胞色素 P450 2D6 抑制剂,IC50 为 0.420 μM,Ki 为 0.535 μM。Rhodiosin 有效的,剂量依赖性抑制乙酰胆碱酯酶 (AChE),IC50 范围为 57.50 至 2.43 μg/mL。Rhodiosin 具有有效的 DPPH 自由基清除活性,IC50 为 27.77 μM。 -
GP10042
Rhodopsin peptide
H2N-Val-Ser-Lys-Thr-Glu-Thr-Ser-Gln-Val-Ala-Pro-Ala-OH
视网膜感光细胞色素;GPCR -
GC72767
Ricasetron
BRL-46470
Ricasetron (BRL-46470)是一种活性化合物。 -
GC31257
Rilmazafone hydrochloride (450191S)
利马扎封盐酸盐,450191S
Rilmazafone hydrochloride (450191S) (450191S) 是苯二氮卓 (omega) 配体。 -
GC48052
Rilmenidine-d4
Oxaminozoline-d4
An internal standard for the quantification of rilmenidine -
GC13802
Riluzole
利鲁唑; PK 26124
Riluzole 是一种抗惊厥药,属于使用依赖性 Na+ 通道阻滞剂家族,它也可以抑制 GABA 摄取,IC50 为 43 μM。 -
GC44841
Riluzole (hydrochloride)
PK 26124 hydrochloride
An inhibitor of glutamatergic transmission -
GC44842
Riluzole-13C,15N2
利鲁唑-13C-15N2
An internal standard for the quantification of riluzole -
GC33775
Rimacalib (SMP 114)
SMP 114
Rimacalib (SMP 114) (SMP 114) 是一种 Ca2+/钙调蛋白依赖性蛋白激酶 II (CaMKII) 抑制剂,IC50 为 ~1 μ;M 代表 CaMKIIα;至 ~30 μ;M 代表 CaMKIIγ;。 -
GC30835
Rislenemdaz (MK-0657)
MK-0657; CERC-301
Rislenemdaz (MK-0657) (CERC-301) 是一种口服生物可利用的选择性 N-甲基-D-天冬氨酸 (NMDA) 受体亚基 2B (GluN2B) 拮抗剂,其 Ki 和 IC 50 分别为 8.1 nM 和 3.6 nM。
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GC31035
Rispenzepine
利喷西平
Rispenzepine是一种选择性毒蕈碱受体(M1和M3受体亚型)拮抗剂。 -
GC12986
Risperidone
利培酮; R 64 766
An atypical antipsychotic -
GC37539
Risperidone hydrochloride
R 64 766 hydrochloride
An atypical antipsychotic -
GC37540
Risperidone mesylate
R 64 766 mesylate
An atypical antipsychotic -
GC48056
Risperidone-d4
利培酮D4,R 64 766-d4
An internal standard for the quantification of risperidone -
GC48401
Risuteganib (trifluoroacetate salt)
ALG-1001
An anti-integrin peptide -
GC13883
Ritanserin
利坦丝林,R 55667
A potent 5-HT2A receptor antagonist -
GC37543
Rivanicline
(E)-位变异烟碱,RJR-2403; (E)-Metanicotine
Rivanicline (RJR-2403) 是神经元烟碱受体,对α4β2亚型有高度选择性,Ki为26 nM,比对α7受体的抑制性高超过1000倍。 -
GC37544
Rivanicline hemioxalate
RJR-2403 hemioxalate; (E)-Metanicotine hemioxalate
Rivanicline hemioxalate (RJR-2403 hemioxalate) 是神经元烟碱受体激动剂,对α4β2亚型有高度选择性,Ki为26 nM,而对α7受体的Ki则为36000 nM。 -
GC10267
Rivastigmine
卡巴拉汀; S-Rivastigmine
A cholinesterase inhibitor -
GC64285
Rivastigmine carbamate impurity
3-硝基苯基乙基(甲基)氨基甲酸酯,3-Nitrophenyl ethyl(methyl)carbamate
Rivastigmine carbamate impurity (3-Nitrophenyl ethyl(methyl)carbamate) 是 Rivastigmine 的杂质。Rivastigmine 是一种具有口服活性的,有效的胆碱酯酶 (ChE) 抑制剂,可抑制丁酰胆碱酯酶 (BChE) 和乙酰胆碱酯酶 (AChE),IC50 分别为 0.037 μM 和 4.15 μM。 -
GC12994
Rivastigmine Tartrate
酒石酸卡巴拉汀; ENA 713; SDZ-ENA 713
A cholinesterase inhibitor -
GC10460
Rizatriptan Benzoate
苯甲酸利扎曲坦,MK 462
A 5-HT1B and 5-HT1D receptor agonist -
GC49413
Rizatriptan N-oxide
利扎曲普坦N氧化物
A potential impurity found in commercial preparations of rizatriptan -
GC48583
Rizatriptan-d6 (benzoate salt)
利扎曲坦苯甲酸盐 d6 (苯甲酸盐)
An internal standard for the quantification of rizatriptan -
GC10980
RJR 2429 dihydrochloride
2-(吡啶-3-基)奎宁基二盐酸盐
An nAChR agonist -
GC10575
RJR-2403 hemioxalate
Neuronal nicotinic receptor agonist
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GC12102
RJR-2403 oxalate
(3E)-N-甲基-4-(3-吡啶基)-3-丁烯-1-胺草酸盐,(E)-Metanicotine oxalate; Rivanicline oxalate; RJR 2403 oxalate
RJR-2403 oxalate (RJR-2403 oxalate; (E)-Metanicotine oxalate) 是一种神经元烟碱受体激动剂,对 α4β2 亚型 (Ki=26 nM) 具有高选择性; > 1,000 倍的选择性比 α7 受体(Ki = 3.6 μM)。 -
GC14383
Ro 01-6128
A positive allosteric modulator of mGLUR1
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GC49277
Ro 04-6790 (hydrochloride hydrate)
A 5-HT6 receptor antagonist
-
GC12428
Ro 10-5824 dihydrochloride
Ro 10-5824 dihydrochloride 是一种选择性多巴胺 D4 受体部分激动剂,Ki 为 5.2 nM。
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GC16780
Ro 15-4513
Ro 15-4513,咪唑并苯二氮卓衍生物,是苯二氮卓受体 (BZR) 的部分反向激动剂。
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GC19310
Ro 25-6981
A potent, NR2B-selective NMDA receptor antagonist
-
GC18410
Ro 25-6981 (maleate)
A potent, NR2B-selective NMDA receptor antagonist
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GC46213
Ro 41-0960
A COMT inhibitor
-
GC19311
Ro 41-1049 hydrochloride
Ro 41-1049 hydrochloride 是单胺氧化酶-A (MAO-A) 的可逆选择性抑制剂。
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GC37547
Ro 41-3290
Ro 41-3290 是一种催眠剂,是 Ro 41-3696 的去甲基化衍生物。Ro 41-3696 是一种苯二氮卓类 (benzodiazepine) 受体的部分激动剂。
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GC11704
Ro 64-5229
mGlu2 antagonist
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GC14172
Ro 67-4853
A positive allosteric modulator of mGlu1 receptors
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GC12485
Ro 67-7476
A positive allosteric modulator of mGluR1
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GC10425
Ro 90-7501
An antiviral useful in Alzheimer’s research