Neuroscience
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
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Neuroscience 相关产品(3932)
- GC35011(Z)-ThiothixeneCAS: 3313-26-6纯度: >97.50%
(Z)-Thiothixene 是 serotonergic receptor 的拮抗剂,来自专利 US 20150141345 A1。
- GC35013[8]-ShogaolCAS: 36700-45-5纯度: >99.50%
[8]-Shogaol,生姜中的一种刺激性酚类化合物,具有抗血小板活性 (IC50=5 μM) 和抑制 COX-2 (IC50=17.5 μM)。[8]-Shogaol 诱导人白血病细胞凋亡。
- GC351927-Hydroxy-3,4-dihydro-2(1H)-quinolinoneCAS: 22246-18-0纯度: >99.50%
7-Hydroxy-3,4-dihydrocarbostyril is used as the materials for the organic synthesis intermediates.
- GC35236AcetylshikoninCAS: 24502-78-1纯度: >98.00%
Acetylshikonin,来源于紫草根,具有抗癌、抗炎作用。Acetylshikonin 是一种非选择性的细胞色素 P450 抑制剂,对所有 P450 亚型抑制的 IC50 值范围为 1.4-4.0 μM。Acetylshikonin 是一种 AChE 抑制剂,具有很强的抗凋亡活性。
- GC35269Agomelatine hydrochlorideCAS: 1176316-99-6纯度: >99.50%
A melatonin receptor agonist and 5-HT 2B and 5-HT 2C antagonist
- GC35270Agomelatine L(+)-Tartaric acidCAS: 824393-18-2纯度: >99.50%
Agomelatine(L(+)-酒石酸)可抗抑郁,是一种去甲肾上腺素-多巴胺抑制解除剂(NDDI),能拮抗5-HT2C受体。
- GC35301Alosetron ((Z)-2-butenedioate)CAS: 122852-43-1
Alosetron (Z)-2-butenedioate (GR 68755 (Z)-2-butenedioate) 是5-HT3受体拮抗剂,可作用于肠易激综合征。
- GC35303Alosetron D3 HydrochlorideCAS: 1189919-71-8
Alosetron D3 Hydrochloride (GR-68755C D3) 是Alosetron氘代化合物标准品。
- GC35323Amisulpride hydrochlorideCAS: 81342-13-4
A dopamine D 2 and D 3 and 5-HT 2B , 5-HT 7 , and 5-HT 7A receptor antagonist
- GC35334Amyloid β Peptide (42-1)(human)CAS: 317366-82-8
淀粉样蛋白 β Peptide (42-1)(human) 是淀粉样蛋白 β 的无活性形式;肽 (1-42)。
- GC35386Aripiprazole D8CAS: 1089115-06-9,1089115-04-7
An internal standard for the quantification of aripiprazole
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC35011 | (Z)-Thiothixene | 3313-26-6 | >97.50% | |
(Z)-Thiothixene 是 serotonergic receptor 的拮抗剂,来自专利 US 20150141345 A1。 | ||||
| GC35012 | [10]-Shogaol | 36752-54-2 | >99.50% | |
A phenol with diverse biological activities | ||||
| GC35013 | [8]-Shogaol | 36700-45-5 | >99.50% | |
[8]-Shogaol,生姜中的一种刺激性酚类化合物,具有抗血小板活性 (IC50=5 μM) 和抑制 COX-2 (IC50=17.5 μM)。[8]-Shogaol 诱导人白血病细胞凋亡。 | ||||
| GC35019 | [Nle11]-Substance P | 57462-42-7 | - | |
[Nle11]-Substance P 是物质 P 类似物,避免了甲硫氨酸氧化问题。 | ||||
| GC35027 | [Sar9] Substance P | 77128-75-7 | - | |
[Sar9] Substance P 是一种有效的选择性神经激肽 (NK)-1 受体激动剂。 | ||||
| GC35192 | 7-Hydroxy-3,4-dihydro-2(1H)-quinolinone | 22246-18-0 | >99.50% | |
7-Hydroxy-3,4-dihydrocarbostyril is used as the materials for the organic synthesis intermediates. | ||||
| GC35222 | ABT-239 | 460746-46-7 | >99.00% | |
ABT-239 是一种新颖的,高效的,非咪唑类的 H3R 拮抗剂,也是 TRPV1 的拮抗剂。 | ||||
| GC35236 | Acetylshikonin | 24502-78-1 | >98.00% | |
Acetylshikonin,来源于紫草根,具有抗癌、抗炎作用。Acetylshikonin 是一种非选择性的细胞色素 P450 抑制剂,对所有 P450 亚型抑制的 IC50 值范围为 1.4-4.0 μM。Acetylshikonin 是一种 AChE 抑制剂,具有很强的抗凋亡活性。 | ||||
| GC35252 | Adoprazine | 222551-17-9 | >98.00% | |
Adoprazine是5-HT1A受体的完全激动剂和D2/3受体的拮抗剂。 | ||||
| GC35256 | Adrenomedullin (11-50), rat | 163648-32-6 | - | |
A truncated form of rat adrenomedullin | ||||
| GC35269 | Agomelatine hydrochloride | 1176316-99-6 | >99.50% | |
A melatonin receptor agonist and 5-HT 2B and 5-HT 2C antagonist | ||||
| GC35270 | Agomelatine L(+)-Tartaric acid | 824393-18-2 | >99.50% | |
Agomelatine(L(+)-酒石酸)可抗抑郁,是一种去甲肾上腺素-多巴胺抑制解除剂(NDDI),能拮抗5-HT2C受体。 | ||||
| GC35272 | Ajmalicine | 483-04-5 | - | |
A terpenoid indole alkaloid | ||||
| GC35279 | Aldicarb sulfone | 1646-88-4 | >99.00% | |
A metabolite of aldicarb | ||||
| GC35284 | Alimemazine D6 | 1346603-88-0 | - | |
Alimemazine D6是Alimemazine氘代化合物标准品。 | ||||
| GC35299 | Aloeresin D | 105317-67-7 | - | |
Aloeresin D 是从芦荟中分离得到的色原酮苷,可抑制 β-分泌酶 (BACE1) 活性,IC50 值为 39 μM。 | ||||
| GC35301 | Alosetron ((Z)-2-butenedioate) | 122852-43-1 | - | |
Alosetron (Z)-2-butenedioate (GR 68755 (Z)-2-butenedioate) 是5-HT3受体拮抗剂,可作用于肠易激综合征。 | ||||
| GC35302 | Alosetron (Hydrochloride(1:X)) | 132414-02-9 | - | |
A 5-HT 3 receptor antagonist | ||||
| GC35303 | Alosetron D3 Hydrochloride | 1189919-71-8 | - | |
Alosetron D3 Hydrochloride (GR-68755C D3) 是Alosetron氘代化合物标准品。 | ||||
| GC35323 | Amisulpride hydrochloride | 81342-13-4 | - | |
A dopamine D 2 and D 3 and 5-HT 2B , 5-HT 7 , and 5-HT 7A receptor antagonist | ||||
| GC35334 | Amyloid β Peptide (42-1)(human) | 317366-82-8 | - | |
淀粉样蛋白 β Peptide (42-1)(human) 是淀粉样蛋白 β 的无活性形式;肽 (1-42)。 | ||||
| GC35381 | Arborine | 6873-15-0 | - | |
Arborine 可从 Glycosmis arborea 中分离。Arborine 抑制乙酰胆碱的外周作用并诱导血压下降。 | ||||
| GC35386 | Aripiprazole D8 | 1089115-06-9,1089115-04-7 | - | |
An internal standard for the quantification of aripiprazole | ||||
| GC35427 | Atropine methyl bromide | 2870-71-5 | - | |
A muscarinic acetylcholine receptor antagonist | ||||
