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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GC91681
Loxoprofen-SRS
Loxoprofen-SRS is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 0.5 and 0.39 for recombinant human COX-1 and COX-2, respectively) and an active metabolite of the prodrug loxoprofen .
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GC72773
LP 12 hydrochloride hydrate
LP 12 hydrochloride hydrate是一种有效的选择性5-HT7受体激动剂,Ki值为0.13 nM。
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GC30880
LP-211
An agonist of 5-HT7 receptors
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GC69400
LP-471756
LP-471756 是一种有效的 GPR139 拮抗剂,IC50 值为 640 nM。LP-471756 抑制 LP-360924 刺激的 cAMP 产生。
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GC39256
LP-935509
LP-935509 是一种小分子衔接蛋白-2 相关激酶1 (AAK1) 选择性和脑渗透抑制剂 (IC50=3.3 nM),一种 ATP 竞争性抑制剂,其 Ki 为 0.9 nM。 LP-935509 是 BIKE 的有效抑制剂 (IC50=14 nM) 和适度的 GAK 抑制剂 (IC50=320 nM)。 LP-935509 可逆转 SNL 手术后的疼痛。
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GC12366
LPYFD-NH2
LPYFD-NH2 是一种五肽,对 Aβ(1-42) 的聚集具有一定的抑制作用。
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GC74062
LSD1/HDAC6-IN-2
LSD1/HDAC6-IN-2(JBI-802)是一种口服活性LSD1/HDAC6/MOA-A抑制剂,IC50值分别为5 nM、11 nM和5 nM。
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GC18309
LSN2463359
N-异丙基-5-(吡啶-4-基乙炔基)吡啶酰胺
A brain penetrant positive allosteric modulator of the mGluR5 -
GC52030
LSN2814617
LSN2814617消旋体
A positive allosteric modulator of mGluR5 receptors -
GC11962
Lu AE58054 Hydrochloride
N-[2-(6-氟-1H-吲哚-3-基)乙基]-3-(2,2,3,3-四氟丙氧基)苄基胺单盐酸盐,Lu AE 58054 Hydrochloride
A 5-HT6 receptor antagonist -
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
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GC12941
Lumiracoxib
罗美昔布; COX-189
A selective inhibitor of COX-2 -
GC44092
Lumula
Maxeyprost, Unoprostone Nethyl amide
A hybrid eicosanoid analog -
GC30926
Lurasidone (SM-13496)
鲁拉西酮; SM-13496
An atypical antipsychotic -
GC17593
Lurasidone HCl
盐酸鲁拉西酮; SM-13496 Hydrochloride
An atypical antipsychotic -
GC41177
Lurasidone metabolite 14283
An active metabolite of lurasidone
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GC47583
Lurasidone-d8
SM-13496-d8
An internal standard for the quantification of lurasidone -
GC44093
Lutein
叶黄素
A carotenoid with diverse biological activities -
GN10022
luteolin-6-C-glucoside
异荭草素; Homoorientin
A flavonoid with diverse biological activities -
GC15998
LX-1031
4-[2-氨基-6-[(1R)-2,2,2-三氟-1-(3'-甲氧基联苯-4-基)乙氧基]嘧啶-4-基]-L-苯丙氨酸,LX1031; LX 1031
LX-1031 是一种有效的、可口服的色氨酸 5-羟化酶 (TPH) 抑制剂,可减少外周血清素 (5-HT) 的合成。 -
GC30884
LX2343
An inhibitor of BACE1 and PI3K
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GC44094
LX7101 (hydrochloride)
A LIMK and ROCK inhibitor
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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。
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GC12770
LY 2087101
Allosteric potentiator of α7, α4β2 and α4β4 nAChRs
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GC14722
LY 2389575 hydrochloride
negative allosteric modulator of mGlu3
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GC50672
LY 2886721 Hydrochloride
N-[3-[(4AS,7AS)-2-氨基-5,7-二氢-4H-呋喃并[3,4-D][1,3]噻嗪-7A(4AH)-基]-4-氟苯基]-5-氟-2-吡啶甲酰胺盐酸盐
An inhibitor of BACE -
GC17039
LY 344864
LY344864;LY-344864
A 5-HT1F receptor antagonist -
GC36501
LY 344864 hydrochloride
A 5-HT1F receptor antagonist
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GC36502
LY 344864 racemate
LY 344864 racemate 是一种 5-HT1F 受体激动剂, 来自专利 US 5708187 A。
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GC36503
LY 344864 S-enantiomer
LY 344864 S-enantiomer 是 LY344864 的 S 型对映体。LY344864 是 5-HT1F 受体激动剂。
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GC10605
LY 354740
(1S,2S,5R,6S)-2-氨基二环[3.1.0]己烷-2,6-二羧酸,LY354740; Eglumetad
An agonist of mGluR2 and mGluR3
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GC12831
LY 367385
An antagonist of mGluR1α
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GC14861
LY 379268
LY 379268是一种高选择性、可透过血脑屏障的II组mGlu受体激动剂,对hmGlu2和hmGlu3的EC50值分别为2.69和4.48nM。
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GC16557
LY 379268 disodium salt
group II mGlu receptor agonist
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GC17492
LY 456236 hydrochloride
mGlu1 receptor antagonist
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GC14097
LY 487379 hydrochloride
LY 487379 hydrochloride 是一种选择性人 mGluR2 正变构调节剂 (PAM)。
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GC13445
LY2119620
3-氨基-5-氯-N-环丙基-4-甲基-6-[2-(4-甲基-1-哌嗪基)-2-氧代乙氧基]-噻吩并[2,3-B]吡啶-2-甲酰胺
A positive allosteric modulator of M2 and M4 mAChRs -
GC41181
LY2183240 2'-isomer
5-([1,1'-联苯]-4-基甲基)-N,N-二甲基-2H-四唑-2-甲酰胺
A less potent, 2,5-regioisomer of LY2183240 -
GC90597
LY2365109 (hydrochloride)
一种GlyT1a抑制剂
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GC17791
LY2811376
(4S)-4-[2,4-二氟-5-(5-嘧啶基)苯基]-5,6-二氢-4-甲基-4H-1,3-噻嗪-2-胺
A BACE1 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 -
GC17138
LY310762
A 5-HT1D antagonist
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GC36510
LY3130481
LY3130481 是一种跨膜 AMPA 受体调节蛋白 TARP γ-8 依赖性的 AMPA 受体拮抗剂,选择性抑制 AMPA/TARP γ-8 的 IC50 值为 65 nM。
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GC63052
LY3154207
LY3154207 是一种有效的、亚型选择性的、口服的人多巴胺 D1 受体 (human dopamine D1 receptor) 正向变构调节剂 (PAM),具有最小的变构激动剂活性 (EC50=3 nM)。
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GC36511
LY334370
4-氟-N-(3-(1-甲基哌啶-4-基)-1H-吲哚-5-基)苯甲酰胺盐酸盐
A 5-HT1F receptor agonist -
GC11182
LY404039
(1R,4S,5S,6S)-4-氨基-2-硫杂双环[3.1.0]己烷-4,6-二甲酸2,2-二氧化物
An agonist of mGluR2 and mGluR3 -
GC45776
LY404187
N-[2-(4'-氰基联苯-4-基)丙基]-2-丙烷磺酰胺
A positive allosteric modulator of AMPA receptors -
GC36515
LY450108
N-[4-[(1R)-1-甲基-2-[[异丙基磺酰基]氨基]乙基]苯基]-3,5-二氟苯基甲酰胺
LY450108是AMPA受体增强剂。 -
GC13010
LY451395
LY451395
LY451395 (LY451395) 是一种有效且高度选择性的 AMPA 受体增强剂。 -
GC64557
Lycoramine
二氢加兰他敏
Lycoramine 是一种从 Lycoris radiate 中分离出的加兰他敏的二氢衍生物。Lycoramine 是一种有效的乙酰胆碱酯酶 (AChE) 抑制剂。