5-羧酰胺色胺马来酸盐结构式
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常用名 | 5-羧酰胺色胺马来酸盐 | 英文名 | 5-Carboxamidotryptamine maleate |
|---|---|---|---|---|
| CAS号 | 74885-72-6 | 分子量 | 319.31 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C15H17N3O5 | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A | |
| 符号 |
GHS07 |
信号词 | Warning |
5-羧酰胺色胺马来酸盐用途5-Carboxamidotryptamine maleate (5-CT maleate) 是一种有效的 5-HT1A,5-HT1B,5-HT1D,5-HT5 和 5-HT7 受体激动剂。 |
| 中文名 | 5-羧酰胺色胺马来酸盐 |
|---|---|
| 英文名 | 5-Carboxamidotryptamine maleate |
| 英文别名 | 更多 |
| 描述 | 5-Carboxamidotryptamine maleate (5-CT maleate) 是一种有效的 5-HT1A,5-HT1B,5-HT1D,5-HT5 和 5-HT7 受体激动剂。 |
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| 相关类别 | |
| 靶点实验 |
5-HT1A Receptor 5-HT1B Receptor 5-HT1D Receptor 5-HT5 Receptor 5-HT7 Receptor |
| 体外研究 | 与牛黑质5-HT1D位点结合的[3H]-5-Carboxamidoryptamine(5-CT)具有快速、可逆和饱和的特点,表现出高亲和力(Kd=0.38nm)和低非特异性结合[2]。在牛黑质中,[3H]-5-甲酰胺三嗪(5-CT)标记的结合位点数量与[3H]-5-Carboxamidoryptamine(分别为403和362fmol/mg蛋白质)的结合位点,并且结合对鸟嘌呤核苷酸敏感[2]。 |
| 体内研究 | 暴露于硬脑膜的外用5-卡波胺(0.01-1000μM)可使麻醉Wistar大鼠的中脑膜动脉舒张压降低,脑膜血流量发生变化,传导率增加(即扩张)(5-羟色胺耗竭,用20 mg/kg皮质酮治疗)[1]。 |
| 参考文献 |
| 分子式 | C15H17N3O5 |
|---|---|
| 分子量 | 319.31 |
| 外观性状 | 固体 |
| 储存条件 | -20°C |
| 符号 |
GHS07 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H315-H319-H335 |
| 警示性声明 | P261-P305 + P351 + P338 |
| 个人防护装备 | dust mask type N95 (US);Eyeshields;Gloves |
| 危害码 (欧洲) | Xi |
| 危险品运输编码 | NONH for all modes of transport |
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GR-127935-sensitive mechanism mediating hypotension in anesthetized rats: are 5-HT5B receptors involved?
J. Cardiovasc. Pharmacol. 65(4) , 335-41, (2015) The 5-HT1B/1D receptor antagonist, GR-127935, inhibits hypotensive responses produced by the 5-HT1A, 5-HT1B/1D and 5-HT7 receptor agonist, and 5-HT5A/5B receptor ligand, 5-carboxamidotryptamine (5-CT)... |
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Synthesis and pharmacological evaluation of optically pure, novel carbonyl guanidine derivatives as dual 5-HT2B and 5-HT7 receptor antagonists.
Bioorg. Med. Chem. 22(21) , 6026-38, (2014) A series of 9-disubstituted N-(9H-fluorene-2-carbonyl)guanidine derivatives have been discovered as potent and orally active dual 5-HT(2B) and 5-HT(7) receptor antagonists. Upon screening several comp... |
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The serotonin receptor 5-HT₇R regulates the morphology and migratory properties of dendritic cells.
J. Cell Sci. 128 , 2866-80, (2015) Dendritic cells are potent antigen-presenting cells endowed with the unique ability to initiate adaptive immune responses upon inflammation. Inflammatory processes are often associated with an increas... |
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实验名称:Thermal Shift Assay. Domain: start/stop: M1-L298
来源:ChEMBL
靶标:Cyclin-dependent kinase 2
External Id:CHEMBL5062802
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实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
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实验名称:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
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实验名称:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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实验名称:Thermal Shift Assay. Domain: start/stop: M1-K294
来源:ChEMBL
靶标:Casein kinase I isoform delta
External Id:CHEMBL5064568
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实验名称:Thermal Shift Assay. Domain: start/stop: M26-R383
来源:ChEMBL
靶标:Glycogen synthase kinase-3 beta
External Id:CHEMBL5065589
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实验名称:Thermal Shift Assay. Domain: start/stop: S229-K512
来源:ChEMBL
靶标:Tyrosine-protein kinase ABL1
External Id:CHEMBL5060015
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实验名称:PDSP Secondary Binding target: ADRA2A - Compounds are tested at 10 uM concentration, ...
来源:ChEMBL
靶标:Alpha-2A adrenergic receptor
External Id:CHEMBL5442194
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实验名称:GPCR beta-arrestin recruitment assay with target: FPR2 Assay Type: PRESTO-Tango Conce...
来源:ChEMBL
靶标:N-formyl peptide receptor 2
External Id:CHEMBL5209826
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| MFCD00069224 |