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)
- GC60596ArecaidineCAS: 499-04-7纯度: >98.00%
Arecaidine,一种吡啶生物碱,是一种有效的GABA吸收抑制剂。Arecaidine是H+偶联的氨基酸转运蛋白1(PAT1,SLC36A1)的底物,竞争性抑制L-脯氨酸的摄取。
- GC60630Befiradol hydrochlorideCAS: 2436760-81-3纯度: >99.50%
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。
- GC60641Betahistine mesylateCAS: 54856-23-4纯度: >98.00%
Betahistine mesylate is the mesylate salt form of Betahistine, a histamine analog and H3 receptor agonist that serves as a vasodilator.
- GC60662Brexpiprazole S-oxideCAS: 1191900-51-2
BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。
- GC60691Cetirizine Impurity CCAS: 83881-59-8
CetirizineImpurityC是Cetirizine的一种杂质。Cetirizine是羟嗪的羧化代谢物,是第二代抗组胺剂。Cetirizine是一种特异的、具有口服活性的H1受体(histamineH1-receptor)的长效拮抗剂。
- GC60740Dapoxetine-D7 hydrochlorideCAS: 129938-20-1纯度: >99.50%
Dapoxetine-D7(LY-210448-D7)hydrochloride是Dapoxetinehydrochloride的氘代物。Dapoxetinehydrochloride是一种短效的选择性5-羟色胺再摄取抑制剂(SSRI)。
- GC60758DeschloroclozapineCAS: 1977-07-7纯度: >98.00%
Deschloroclozapine是一种高亲和力、选择性且代谢稳定的毒蕈碱DREADD激动剂,Deschloroclozapine能快速穿透血脑屏障,有效激活兴奋性hM3Dq和抑制性hM4Di DREADD受体。
- GC60774Dihydro DonepezilCAS: 120012-04-6
DihydroDonepezil(DihydroE2020)是Donepezil的代谢产物。Donepezil是一种有效的特异性AChE抑制剂,对bAChE和hAChE的IC50分别为8.12nM和11.6nM。
- GC60791Doxepin D3 HydrochlorideCAS: 347840-07-7
DoxepinD3Hydrochloride是DoxepinHydrochloride的氘代物。Doxepinhydrochloride是一种口服活性的三环抗抑郁药。Doxepinhydrochloride是一种有效的选择性组胺受体H1拮抗剂。Doxepinhydrochloride也是一种有效的CYP450抑制剂,并显着抑制CYP4502C19和CYP4501A2。
- GC60846FlesinoxanCAS: 98206-10-1纯度: >99.00%
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。
- GC60862GABAA receptor agent 1CAS: 1571-87-5纯度: >98.50%
GABAA receptor agent 1 is a high affinity ligand for Gamma-aminobutyric acid A (GABAA) receptor that exerts potent anticonvulsant activity.
- GC60866Gap 26 TFA纯度: >98.00%
Gap 26, a connexin mimetic peptide that composeds of residue no. 63-75 of the extracellular loop 1 of connexin 43 (Cx43), is a gap junction inhibitor. Gap 26 blocks photoliberating inositol-1,4,5-trisphosphate triggers ATP release.
- GC60913Huperzine CCAS: 163089-71-2
HuperzineC是从Huperziaserrate中分离的一种生物碱。HuperzineC是一种乙酰胆碱酯酶(AChE)抑制剂,其IC50值为0.6μM。HuperzineC可用于阿尔茨海默症的研究。
- GC60915Hydroxy ziprasidoneCAS: 884305-08-2
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。
- GC60917Hydroxyamine hydrochlorideCAS: 5470-11-1纯度: >99.00%
Hydroxylammonium chloride (Hydroxylamine hydrochloride) is the hydrochloric acid salt of hydroxylamine, which is a biological intermediate in the nitrification and in the anammox.
- GC60926Ibuprofen impurity 1CAS: 3585-47-5
Ibuprofenimpurity1是Ibuprofen的杂质。Ibuprofen是COX-1和COX-2的抑制剂,IC50值分别为13μM和370μM,具有抗炎的活性。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60592 | APS6-45 | 2188236-41-9 | >99.50% | |
APS6-45(Compound 10) is an orally active tumor-calibrated inhibitor (TCI) that inhibits RAS/MAPK signaling and exhibits antitumor activity. | ||||
| GC60596 | Arecaidine | 499-04-7 | >98.00% | |
Arecaidine,一种吡啶生物碱,是一种有效的GABA吸收抑制剂。Arecaidine是H+偶联的氨基酸转运蛋白1(PAT1,SLC36A1)的底物,竞争性抑制L-脯氨酸的摄取。 | ||||
| GC60630 | Befiradol hydrochloride | 2436760-81-3 | >99.50% | |
Befiradolhydrochloride(NLX-112hydrochloride)是选择性的5-羟色胺1A(5-HT)1A受体激动剂。 | ||||
| GC60641 | Betahistine mesylate | 54856-23-4 | >98.00% | |
Betahistine mesylate is the mesylate salt form of Betahistine, a histamine analog and H3 receptor agonist that serves as a vasodilator. | ||||
| GC60662 | Brexpiprazole S-oxide | 1191900-51-2 | - | |
BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。 | ||||
| GC60691 | Cetirizine Impurity C | 83881-59-8 | - | |
CetirizineImpurityC是Cetirizine的一种杂质。Cetirizine是羟嗪的羧化代谢物,是第二代抗组胺剂。Cetirizine是一种特异的、具有口服活性的H1受体(histamineH1-receptor)的长效拮抗剂。 | ||||
| GC60709 | Cinnarizine D8 | 1185242-27-6 | - | |
An internal standard for the quantification of cinnarizine | ||||
| GC60723 | COR659 | 544450-68-2 | >99.50% | |
COR659是GABAB的阳性变构调节剂(PAM)。COR659可缓解大鼠对酒精和巧克力的药物成瘾。 | ||||
| GC60740 | Dapoxetine-D7 hydrochloride | 129938-20-1 | >99.50% | |
Dapoxetine-D7(LY-210448-D7)hydrochloride是Dapoxetinehydrochloride的氘代物。Dapoxetinehydrochloride是一种短效的选择性5-羟色胺再摄取抑制剂(SSRI)。 | ||||
| GC60758 | Deschloroclozapine | 1977-07-7 | >98.00% | |
Deschloroclozapine是一种高亲和力、选择性且代谢稳定的毒蕈碱DREADD激动剂,Deschloroclozapine能快速穿透血脑屏障,有效激活兴奋性hM3Dq和抑制性hM4Di DREADD受体。 | ||||
| GC60774 | Dihydro Donepezil | 120012-04-6 | - | |
DihydroDonepezil(DihydroE2020)是Donepezil的代谢产物。Donepezil是一种有效的特异性AChE抑制剂,对bAChE和hAChE的IC50分别为8.12nM和11.6nM。 | ||||
| GC60791 | Doxepin D3 Hydrochloride | 347840-07-7 | - | |
DoxepinD3Hydrochloride是DoxepinHydrochloride的氘代物。Doxepinhydrochloride是一种口服活性的三环抗抑郁药。Doxepinhydrochloride是一种有效的选择性组胺受体H1拮抗剂。Doxepinhydrochloride也是一种有效的CYP450抑制剂,并显着抑制CYP4502C19和CYP4501A2。 | ||||
| GC60846 | Flesinoxan | 98206-10-1 | >99.00% | |
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。 | ||||
| GC60862 | GABAA receptor agent 1 | 1571-87-5 | >98.50% | |
GABAA receptor agent 1 is a high affinity ligand for Gamma-aminobutyric acid A (GABAA) receptor that exerts potent anticonvulsant activity. | ||||
| GC60866 | Gap 26 TFA | - | >98.00% | |
Gap 26, a connexin mimetic peptide that composeds of residue no. 63-75 of the extracellular loop 1 of connexin 43 (Cx43), is a gap junction inhibitor. Gap 26 blocks photoliberating inositol-1,4,5-trisphosphate triggers ATP release. | ||||
| GC60875 | GKT136901 | 955272-06-7 | >99.00% | |
A dual inhibitor of NOX1 and NOX4 | ||||
| GC60886 | GSK356278 | 720704-34-7 | >99.50% | |
A selective PDE4 inhbitor | ||||
| GC60890 | Guvacine | 498-96-4 | - | |
An inhibitor of GABA uptake | ||||
| GC60913 | Huperzine C | 163089-71-2 | - | |
HuperzineC是从Huperziaserrate中分离的一种生物碱。HuperzineC是一种乙酰胆碱酯酶(AChE)抑制剂,其IC50值为0.6μM。HuperzineC可用于阿尔茨海默症的研究。 | ||||
| GC60915 | Hydroxy ziprasidone | 884305-08-2 | - | |
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。 | ||||
| GC60917 | Hydroxyamine hydrochloride | 5470-11-1 | >99.00% | |
Hydroxylammonium chloride (Hydroxylamine hydrochloride) is the hydrochloric acid salt of hydroxylamine, which is a biological intermediate in the nitrification and in the anammox. | ||||
| GC60924 | Hydroxyzine D8 | 1189480-47-4 | - | |
An internal standard for the quantification of hydroxyzine | ||||
| GC60926 | Ibuprofen impurity 1 | 3585-47-5 | - | |
Ibuprofenimpurity1是Ibuprofen的杂质。Ibuprofen是COX-1和COX-2的抑制剂,IC50值分别为13μM和370μM,具有抗炎的活性。 | ||||
| GC60935 | Indomethacin sodium hydrate | 74252-25-8 | >98.00% | |
A non-selective COX inhibitor | ||||
