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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GC31049
RWJ-51204
RWJ-51204是GABA(A)receptor的部分激动剂,Ki值为0.2-2nM。
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GC48063
S 14506
A 5-HT1A receptor agonist
-
GC18013
S 14506 hydrochloride
A 5-HT1A receptor agonist
-
GC13684
S 18986
A positive allosteric modulator of AMPA receptors
-
GC15910
S 24795
2-[2-(4-溴苯肼)-2-乙氧基]-1-甲基碘吡啶
S 24795 是 α7 nAChR 的部分激动剂,可改善老年小鼠的记忆功能,用于治疗与衰老相关的记忆障碍。 -
GC31105
S 38093
S 38093 is a histamine H3 antagonist/inverse agonist with a moderate affinity for rat, mouse and human H3 receptors (Ki = 8.8, 1.44 and 1.2 μM, respectively) and no affinity for other histaminergic receptors.
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GC30027
S-(+)-Marmesin ((+)-Marmesin)
异紫花前胡内酯,(+)-Marmesin; (S)-Marmesin
A coumarin with anticancer activity -
GC18650
S-(5'-Adenosyl)-L-methionine (tosylate)
AdoMet, SAM, SAMe
S-Adenosyl-L-methioninetosylate(S-Adenosylmethioninetosylate)是通过蛋氨酸腺苷转移酶的作用由蛋氨酸和ATP内源性生产的,是一种重要的具有口服活性的甲基供体。
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GC31835
S-2474
S-2474是COX-2和5-lipoxygenase的抑制剂,在人完整的细胞中,对COX-2和COX-1的IC50值分别为11nM和27μM,为一种非甾体抗炎药。
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GC31121
S-8510 phosphate (SB-737552 phosphate)
SB-737552 phosphate
S-8510 (phosphate) 是一种反向苯二氮卓 (BDZ) 受体激动剂,对 -GABA 和 +GABA 的 Kis 分别为 34.6 nM、36.2 nM。 -
GC52033
S-Methyl-D-penicillamine
A metabolite of D-penicillamine
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GC10026
S-Sulfo-L-cysteine sodium salt
EAA receptor agonist
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GC31313
S16961 (S169611)
S169611
S16961 (S169611) 是一种烟碱受体激动剂。 -
GC90638
S1H (trifluoroacetate salt)
Site 1-binding Helix
一种生长激素受体的合成肽拮抗剂
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GC69852
Sabcomeline hydrochloride
SB-202026 hydrochloride; Memric hydrochloride
Sabcomeline (SB-202026) hydrochloride 是一种有效的功能性选择性 M1 毒蕈碱受体受体 ( muscarinic M1 receptor) 部分激动剂,可以改善认知功能。Sabcomeline hydrochloride 可用于阿尔茨海默症的研究。 -
GC49093
Safflower Red
红花黄色素
Safflower red是从番红花(Carthamus tinctorius)的花朵中提取的活性物质。 -
GC13016
Safinamide
沙芬酰胺; FCE 26743; EMD 1195686
Safinamide 是一种强效、选择性和可逆的单胺氧化酶 B (MAO-B) 抑制剂 (IC50=0.098 μM),优于 MAO-A (IC50=580 μM)。 -
GC49756
Safinamide Acid
沙芬酰胺杂质5
A potential impurity found in commercial preparations of safinamide -
GC90480
Safinamide Metabolite NW 1689
商业制备的沙非胺中发现了潜在杂质。
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GC45557
Safinamide-d4
沙芬酰胺 d4
An internal standard for the quantification of safinamide -
GC19318
SAGE-217
S-812217, SGE 797
A positive allosteric modulator of GABAA receptors -
GN10502
Saikosaponin C
柴胡皂苷 C
A saikosaponin with anti-inflammatory and analgesic activities -
GC48374
Saikosaponin D (hydrate)
A triterpene saponin with diverse biological activities
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GC16508
Salicylic acid
水杨酸; 2-Hydroxybenzoic acid
An Analytical Reference Standard -
GC74187
Salicylic acid-13C6
2-Hydroxybenzoic acid-13C6
Salicylic acid-13C6是13c标记的水杨酸。 -
GC49480
Salicylic Acid-d4
水杨酸-D4
An internal standard for the quantification of salicylic acid -
GC64032
Salicylic acid-d6
水杨酸-D6; 2-Hydroxybenzoic acid-d6
Salicylic acid-D6 (2-Hydroxybenzoic acid-D6) 是 Salicylic acid 的一种氘代化合物。Salicylic acid 抑制 COX-2 活性,抑制作用与转录因子 (NF-κB) 激活无关。 -
GC49363
Salicyluric Acid
2-羟基马尿酸
A major metabolite of aspirin and salicylic acid -
GC33749
Salsolidine
猪毛菜定;鹿尾草定
An alkaloid -
GC11269
Salsolinol-1-carboxylic acid
Salsolinol-1-carboxy acid 是中枢神经系统 (CNS) 中的一种内源性生物碱。
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GC44869
Salvinorin A Carbamate
A potent KOR agonist
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GC44870
Salvinorin A Propionate
Salvinorinyl-2-propionate
A selective κ1-opioid receptor partial agonist -
GC44871
Salvinorin B Mesylate
Mesyl Sal B
A κ-opioid receptor agonist -
GC64084
Samelisant
SUVN-G3031
Samelisant (SUVN-G3031) 是一种口服有效的,可通过血脑屏障的选择性组胺 H3 受体 (H3R) 反向激动剂。Samelisant 对人类 (hH3R; Ki=8.7 nM) 和大鼠 (rH3R; Ki=9.8 nM) H3R 具有相似的结合亲和力,表明没有种间差异。 Samelisant 可用于研究睡眠相关疾病。 -
GC48351
Saralasin (trifluoroacetate salt)
Aralasin, 1-Sar-8-Ala-Angiotensin II
A peptide AT2 receptor agonist -
GC31143
Saredutant (SR 48968)
SR 48968; SR 48968C
Saredutant (SR 48968) 是一种选择性(Neurokinin 2) NK2受体拮抗剂,IC50值为0.13nM。 -
GC64530
Sarizotan
EMD 128130
Sarizotan (EMD 128130) 是具有口服活性的 5-HT1A 受体 和多巴胺受体的激动剂,其 IC50 值分别为 6.5 nM (rat 5-HT1A)、 0.1 nM (human 5-HT1A)、15.1 nM (rat D2)、17 nM (human D2)、6.8 nM (human D3) 和 2.4 nM (human D4.2)。 -
GC31112
Sarmazenil (Ro 15-3505)
沙马西尼,Ro 15-3505
Sarmazenil (Ro 15-3505) 是一种苯二氮卓受体拮抗剂。 -
GC16202
Sarpogrelate hydrochloride
盐酸沙格雷酯; MCI-9042
A selective 5-HT2 receptor antagonist -
GC49679
Sauvagine (trifluoroacetate salt)
A neuropeptide hormone
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GC14342
Sazetidine A dihydrochloride
α4β2 nicotinic acetylcholine receptor ligand
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GC25898
SB 200646
SB 200646A
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo. -
GC18273
SB 202190 (hydrochloride)
A potent and selective p38 MAP kinase inhibitor
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GC50014
SB 215505
6-氯-2,3-二氢-5-甲基-N-5-喹啉基-1H-吲哚-1-甲酰胺
SB 215505 是一种有效的亚型选择性 5-HT2B 受体拮抗剂,对 5-HT2B、5-HT2A、5-HT2C 的 pKi 值分别为 8.3、6.77、7.66。 -
GC13438
SB 224289 hydrochloride
SB-224289A
A 5-HT1B receptor inverse agonist -
GC14392
SB 242084
6-氯-2,3-二氢-5-甲基-N-[6-[(2-甲基-3-吡啶基)氧]-3-吡啶基]-1H-吲哚-1-酰胺盐酸盐
Specific antagonist of 5-HT2C -
GC61268
SB 243213
A 5-HT2C receptor inverse agonist
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GC37596
SB 258719
SB 258719 是一个有选择性的 5-HT7 受体拮抗剂,其 pKi 值为 7.5。
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GC37597
SB 271046 Hydrochloride
5-氯-N-[4-甲氧基-3-(1-哌嗪基)苯基]-3-甲基苯并[B]噻吩-2-磺酰胺盐酸盐,SB 271046A
An orally-available 5-HT6 antagonist -
GC13183
SB 277011A dihydrochloride
SB-277011A dihydrochloride
A selective dopamine D3 antagonist