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
-
GC17599
Haloperidol
氟哌啶醇
Haloperidol是一种典型的抗精神病药和多巴胺D2样受体拮抗剂,也是离子通道抑制剂,可抑制多种离子通道,如G蛋白激活的内向整流钾通道、钙激活钾通道、HERG和HEAG钾通道以及L、N和P型钙通道。 -
GC10659
Fosaprepitant dimeglumine salt
福沙吡坦二甲葡胺; MK-0517; L785298
A prodrug form of aprepitant -
GC16246
Fosaprepitant
福沙吡坦; L-758298
A prodrug form of aprepitant -
GC12091
SB742457
3-苯基磺酰基-8-(哌嗪-1-基)喹啉,SB-742457; GSK-742457; RVT-101
A 5-HT6 receptor antagonist -
GC16797
Escitalopram Oxalate
依他普仑草酸盐; (S)-Citalopram oxalate; (S)-(+)-Citalopram oxalate
A selective serotonin reuptake inhibitor -
GC13161
Escitalopram
艾司西酞普兰; (S)-Citalopram; (S)-(+)-Citalopram
A selective serotonin reuptake inhibitor -
GC13533
Cisapride
西沙比利; R 51619; (±)-Cisaprid
A 5-HT4 receptor agonist -
GC14096
Aclidinium Bromide
阿地溴铵; LAS 34273; LAS-W 330
A muscarinic acetylcholine receptor antagonist -
GC15434
A 839977
A P2X7 receptor antagonist
-
GC16819
VU0152100
3-氨基-N-[(4-甲氧基苯基)甲基]-4,6-二甲基噻吩并[2,3-B]吡啶-2-甲酰胺,VU152100
A muscarinic M4 receptor positive allosteric modulator -
GC17130
BRL-54443
3-(1-甲基-4-哌啶基)-1H-吲哚-5-醇
A potent agonist of 5-HT1E and 5-HT1F -
GC17184
Ambrisentan
安倍生坦; BSF 208075; LU 208075
An ETA receptor antagonist -
GC10621
Biperiden HCl
盐酸比哌立登; KL 373 hydrochloride
A muscarinic acetylcholine receptor antagonist
-
GC16226
BRL-15572 dihydrochloride
BRL15572盐酸盐
A 5-HT1D receptor antagonist -
GC16986
SDZ 220-581 hydrochloride
(S)-ALPHA-氨基-2'-氯-5-(膦酰甲基)-[1,1'-联苯]-3-丙酸盐酸盐
SDZ 220-581 hydrochloride 是一种口服有效的竞争性 NMDA 受体拮抗剂,pKi 值为 7.7。 -
GC11643
PNU-120596
NSC 216666
PNU-120596是α7神经元烟碱乙酰胆碱受体(α7nAChR)的正变构调节剂,EC50值为216nM。 -
GC17769
Sitaxentan sodium
西他生坦钠,IPI 1040 sodium; TBC11251 sodium
Sitaxentan sodium是一种选择性内皮素A受体(ETA)拮抗剂(IC50 = 1.4nM;Ki = 0.43nM)。 -
GC17695
Aniracetam
茴拉西坦; Ro 13-5057
An Analytical Reference Standard -
GC11192
MK-3207 HCl
(8R)-8-(3,5-二氟苯基)-10-氧代-N-[(2R)-1,1',2',3-四氢-2'-氧代螺[2H-茚-2,3'-[3H]吡咯并[2,3-B]吡啶]-5-基]-6,9-二氮杂螺[4.5]癸烷-9-乙酰胺盐酸盐
MK-3207 (Hydrochloride) 是一种有效的口服生物可利用的 CGRP 受体拮抗剂,IC50 为 0.12 nM,Ki 为 0.024 nM,对人 AM1、AM2、CTR 和 AMY3 具有高度选择性。 -
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。 -
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。 -
GC10264
Arecoline hydrobromide
氢溴酸槟榔碱
Muscarinic acetylcholine receptor agonist -
GC14714
Bupropion hydrochloride
盐酸氨非他酮; Amfebutamone hydrochloride
An Analytical Reference Material -
GC10698
Cyproheptadine hydrochloride
盐酸赛庚啶
An antihistamine with antiserotonergic and anticholinergic activities -
GC10198
Memantine hydrochloride
盐酸美金刚; D-145 hydrochloride
An NMDA receptor antagonist -
GC10575
RJR-2403 hemioxalate
Neuronal nicotinic receptor agonist
-
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 -
GC17456
NMDA (N-Methyl-D-aspartic acid)
N-甲基-D-天冬氨酸; N-Methyl-D-aspartic acid
An excitatory neurotransmitter -
GC13793
NH125
An antibacterial imidazole
-
GC12391
Xanthohumol
黄腐醇
A natural prenylated chalcone
-
GC12717
Ipratropium Bromide
异丙托溴铵; Sch 1000
A muscarinic receptor antagonist -
GC13871
Duloxetine HCl
盐酸度洛西汀; (S)-Duloxetine hydrochloride; LY-248686 hydrochloride
A serotonin and norepinephrine reuptake inhibitor -
GC14984
Diphenylpyraline HCl
盐酸双苯比拉林,4-Diphenylmethoxy-1-methylpiperidine hydrochloride
A histamine H1 receptor antagonist -
GC16635
Diphemanil Methylsulfate
甲硫二苯马尼,Diphemanil mesylate
An anticholinergic agent -
GC15312
Chlorprothixene
氯普噻吨
A dopamine D2 receptor antagonist -
GC10624
Carbenoxolone disodium
甘珀酸钠
An 11β-HSD inhibitor -
GC14160
Blonanserin
布南色林; AD-5423
A dopamine and serotonin receptor antagonist -
GC11977
Thioridazine HCl
盐酸硫利达嗪;盐酸硫代利哒;甲硫达嗪盐酸盐;甲硫哒嗪盐酸盐
A typical antipsychotic -
GC10978
Terfenadine
特非那定; (±)-Terfenadine; MDL-991
A selective histamine H1-receptor antagonist -
GC10460
Rizatriptan Benzoate
苯甲酸利扎曲坦,MK 462
A 5-HT1B and 5-HT1D receptor agonist -
GC12994
Rivastigmine Tartrate
酒石酸卡巴拉汀; ENA 713; SDZ-ENA 713
A cholinesterase inhibitor -
GC12986
Risperidone
利培酮; R 64 766
An atypical antipsychotic -
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。 -
GC16790
Piroxicam
吡罗昔康; CP-16171
A COX inhibitor and NSAID -
GC10112
Paliperidone
9-羟基利培酮; 9-Hydroxyrisperidone
An atypical antipsychotic -
GC14113
Oxybutynin
奥昔布宁
An antagonist of muscarinic acetylcholine receptors -
GC11762
Meloxicam (Mobic)
美洛昔康
A selective COX-2 inhibitor -
GC17227
LY2886721
N-[3-[(4AS,7AS)-2-氨基-4A,5-二氢-4H-呋喃并[3,4-D][1,3]噻嗪-7A(7H)-基]-4-氟苯基]-5-氟-2-吡啶甲酰胺
An inhibitor of BACE -
GC15095
Levodopa
左旋多巴; Levodopa; 3,4-Dihydroxyphenylalanine
A dopamine precursor