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(419)
- AChR(53)
- AChE(100)
- Alzheimer(103)
- Amyloid β(118)
- BACE(4)
- CGRP (33)
- COX(291)
- DAPK(7)
- Dopamine Receptor(289)
- GABA Receptor(154)
- Gap Junction(16)
- GluR(117)
- 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(19)
- Monoamine Oxidase(91)
- Serotonin Transporter(57)
- nAChR(99)
- iGluR(155)
- Neurokinin Receptor(75)
- MCHR1 (GPR24)(16)
- mAChR(183)
- GPR139(4)
- Cholecystokinin Receptor(25)
- Behavioral Neuroscience(348)
- DREADD(1)
- Huntington(13)
- Neuroendocrinology(63)
- Neuroprotection(114)
- Ophthalmology(151)
- Pain Research(223)
- Parkinson(73)
- Prion(7)
- Seizure Disorders(93)
- Cholinesterases(13)
- Tau Protein(4)
- Neurodegenerative Disorders(5)
- Cholinesterase (ChE)(4)
- Amyloid-β(9)
- γ-secretase(1)
- Ischemia(3)
- Cat.No. 产品名称 Information
-
GC30847
IC87201
An inhibitor of the nNOS-PSD-95 protein-protein interaction
-
GC30844
Afloqualone
氟喹酮; HQ-495
An Analytical Reference Standard
-
GC30840
Quinagolide hydrochloride (CV205-502 hydrochloride)
盐酸喹高利特; CV205-502 hydrochloride
Quinagolide hydrochloride (CV205-502 hydrochloride) 是一种选择性多巴胺 D2 受体激动剂,也是一种催乳素抑制剂。
-
GC30839
Traxoprodil
曲索罗地
An antagonist of NR2B subunit-containing NMDA receptors
-
GC30836
MK-7622 (M1 receptor modulator)
3-[(1S,2S)-2-羟基环己基]-6-[(6-甲基-3-吡啶基)甲基]苯并[H]喹唑啉-4(3H)-酮,M1 receptor modulator
A positive allosteric modulator of M1 mAChRs
-
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。
-
GC30827
Pipequaline (PK-8165)
哌夸林,PK-8165
A partial agonist of central benzodiazepine receptors
-
GC30826
Temanogrel (APD791)
APD791
Temanogrel (APD791) 是一种高度选择性的 5-HT2A 受体拮抗剂,Ki 为 4.9 nM。
-
GC30824
Veralipride ((±)-Veralipride)
维拉必利,(±)-Veralipride; LIR166
Veralipride ((±)-Veralipride) 是一种 D2 受体拮抗剂。
-
GC30823
Edonerpic maleate (T-817 maleate)
1-(3-(2-(苯并[B]噻吩-5-基)乙氧基)丙基)氮杂环丁烷-3-醇马来酸,T-817 maleate; T-817MA
T-817MA propyl}-3-azetidinol maleate] 是一种新合成的阿尔茨海默病 (AD) 治疗剂,具有神经保护作用β-淀粉样肽 (Aβ) 的毒性和促进神经突生长的作用.T-817MA 预处理 24 小时后,T-817MA 在 0.1 和 1 uM 时显着防止 H2O2 处理引起的神经元损伤。
-
GC30822
Solifenacin (YM905)
索利那新; YM905 free base
Solifenacin (YM905) is a competitive muscarinic receptor antagonist. The binding of acetylcholine to these receptors, particularly the M3 receptor subtype, plays a critical role in the contraction of smooth muscle.
-
GC30821
JNJ-39758979
JNJ-39758979是一个有选择性且具有高亲和性的组胺H4受体拮抗剂,其Ki值为12.5nM。
-
GC30818
ZL006
An nNOS/PSD-95 interaction inhibitor
-
GC30812
Imidafenacin (KRP-197)
咪达那新; KRP-197; ONO-8025
Imidafenacin (KRP-197, ONO-8025) is a urinary antispasmodic of the anticholinergic class. It is a novel antimuscarinic agent with safety and efficacy, has been clinically used for the treatment of overactive bladder. Imidafenacin(KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM; less potent for M2 receptors(IC50=4.13 nM). IC50 value: 0.3 nM(M3).
-
GC30810
Donepezil (E2020)
多奈哌齐; E2020 free base
Donepezil (E2020)是一种乙酰胆碱酯酶(AChE)抑制剂,IC50为6.7nM。
-
GC30809
VU0467154
5-氨基-3,4-二甲基-噻吩并[2,3-C]哒嗪-6-羧酸4-三氟甲磺酰基-苄基酰胺
A positive allosteric modulator of the M4 muscarinic acetylcholine receptor
-
GC30807
ZSET1446 (ST-101)
ST-101
ZSET1446 (ST-101) 是一种新型认知增强剂,可显着改善各种类型的阿尔茨海默病 (AD) 模型中的学习缺陷。
-
GC30797
lumateperone Tosylate (ITI-007)
1-(4-氟苯基)-4-[(6BR,10AS)-2,3,6B,9,10,10A-六氢-3-甲基-1H-吡啶并[3',4':4,5]吡咯并[1,2,3-DE]喹喔啉-8(7H)-基]-1-丁酮对甲苯磺酸盐,ITI-007 tosylate
An atypical antipsychotic
-
GC30796
Nelotanserin (APD125)
1-[3-(4-溴-1-甲基-1H-吡唑-5-基)-4-甲氧基苯基]-3-(2,4-二氟苯基)脲,APD125
Nelotanserin (APD125) 是一种有效的 5-HT2A 反向激动剂、中度有效的 5-HT2C 部分反向激动剂和弱 5-HT2B 反向激动剂,在 IP 积累试验中 IC50 分别为 1.7、79、791 nM。
-
GC30790
Triflupromazine hydrochloride
盐酸三氟丙嗪
A phenothiazine with diverse biological activities
-
GC30788
L-Glutamic acid monosodium salt (Monosodium glutamate)
谷氨酸单钠盐
L-Glutamic acid monosodium salt is the sodium salt of glutamic acid, found naturally in tomatoes, cheese and other foods. L-Glutamic acid monosodium salt acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). (S)-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals.
-
GC30787
Sertindole (Lu 23-174)
舍吲哚; Lu 23-174
An atypical antipsychotic
-
GC30780
Fipexide
非哌西特
Fipexide (hydrochloride) is a psychoactive drug of the piperazine class.
-
GC30775
Histamine (Ergamine)
组胺; Ergamine
A biogenic amine
-
GC30774
Tat-NR2B9c
Tat-NR2Bct; NA-1
Tat-NR2B9c 旨在通过阻止突触后密度蛋白 95 (PSD-95) 与 N-甲基-D-天冬氨酸 (NMDA) 受体和神经元一氧化氮结合来阻止一氧化氮 (NO) 的产生氧化物合成酶。
-
GC30773
Phenelzine sulfate
硫酸苯乙肼
Phenelzine sulfate是一种单胺氧化酶(MAO)抑制剂。
-
GC30772
Dopamine serotonin antagonist-1
氯氮平杂质,Deschloroclozapine
Deschloroclozapine, a metabolite of Clozapine, is a highly potent muscarinic DREADDs (muscarinic Designer Receptors Exclusively Activated by Designer Drugs) agonist, and binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively.
-
GC30766
Tranylcypromine hemisulfate (dl-Tranylcypromine hemisulfate)
反苯环丙胺半硫酸盐; SKF 385 hemisulfate
Tranylcypromine (Parnate) is an irreversible inhibitor of monoamine oxidase (MAO) with a rapid onset of activity.
-
GC30762
Harmine (Telepathine)
去氢骆驼蓬碱; Telepathine
A unique regulator of PPARγ expression
-
GC30759
H3 receptor-MO-1
H3receptor-MO-1是一种组胺H3受体(histamineH3receptor)调节剂。
-
GC30752
CCK-B Receptor Antagonist 1
(Rac)-Netazepide; (Rac)-YF 476; (Rac)-YM-220
CCK-B Receptor Antagonist 1 是胆囊收缩素 B (CCK-B) 受体的拮抗剂,具有减少胃酸分泌的潜力。
-
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。
-
GC30680
Gastrin/CCK antagonist 1
Gastrin/CCKantagonist1是gastrin/CCK的拮抗剂,可用于肠胃失调疾病的研究。
-
GC30674
CHEMBL333994 (FK-480)
FK-480
CHEMBL333994 (FK-480) 是一种有效的口服有效的胆囊收缩素 A (CCK-A) 拮抗剂,IC50 为 0.67 nM。
-
GC30610
LY 178002
LY178002是一种有效的5-lipoxygenase,phospholipaseA2抑制剂,对5-lipoxygenase的IC50值为0.6μM,能够抑制人多形核白细胞产生LTB4,同时可相对较弱地抑制cyclooxygenase的活性。
-
GC30544
(2-Chloropyridin-4-yl)methanamine hydrochloride
2-氯-4-氨甲基吡啶; LOXL2-IN-1 hydrochloride
(2-Chloropyridin-4-yl)methanamine hydrochloride是一种高选择性的赖氨酰氧化酶样蛋白-2(LOXL2)抑制剂,其IC50为126nM。
-
GC30521
Broflanilide
氟苯双酰胺
Broflanilide是一种杀虫剂,可以分解成desmethyl-broflanilide,为特异性的昆虫耐狄氏剂的GABAreceptor拮抗剂,抑制斜纹夜蛾RDLGABAR,IC50值为1.3nM。
-
GC30496
Doxylamine D5 succinate
琥珀酸多西拉敏 D5
DoxylamineD5琥珀酸盐是Doxylamine氘代化合物标准品。
-
GC30457
Zonampanel (YM 872)
唑南帕奈; YM 872
Zonampanel (YM 872) (YM 872) 是谷氨酸受体亚型 α;-氨基-3-羟基-5-甲基异恶唑-4-丙酸 (AMPA) 受体的选择性拮抗剂。
-
GC30455
Rocastine (AHR-11325)
罗卡斯汀,AHR-11325
Rocastine (AHR-11325) 是一种选择性、非镇静 H1 拮抗剂,用作抗组胺药。
-
GC30446
MHP 133
MHP133是一种多靶点抑制剂,可以抑制AChE的活性,KKi值为69μM;同时抑制毒蕈碱M1和M2受体,5HT4受体和咪唑I2受体。
-
GC30433
Ru-32514
Ru-32514是一种苯二氮受体(benzodiazepinereceptor)激动剂。
-
GC30426
YM-58790
YM-58790是一种有效的M3muscarinic受体拮抗剂,Ki值为15nM。
-
GC30423
CP-66948
CP-66948是histamineH2受体拮抗剂,能够抑制胃酸分泌,保护粘膜的作用。
-
GC30413
Dolasetron Mesylate (MDL-73147EF)
甲磺酸多拉司琼,MDL-73147EF
A 5-HT3 receptor antagonist
-
GC30412
Dolasetron (MDL-73147)
多拉司琼,MDL-73147
A 5-HT3 receptor antagonist
-
GC30409
Elucaine
普罗卡因
Elucaine是蕈毒碱型乙酰胆碱受体(mAChR)拮抗剂,具有抗溃疡功效。
-
GC30396
Piribedil D8 (ET-495 D8)
吡贝地尔D8,ET-495 D8
Piribedil D8 (ET-495 D8) (ET-495 D8) 是氘标记的 Piribedil,它是一种抗帕金森病药物。
-
GC30392
Desmethoxyyangonin (Demethoxyyangonin)
去甲氧基醉椒素,Demethoxyyangonin; 5,6-Dehydrokavain
An Analytical Reference Standard
-
GC30375
Clomipramine D3
Chlorimipramine-d3; G-34586-d3; NSC-169865-d3
An Analytical Reference Standard