Mesdopetam hemitartrate
CAS No. 2562346-14-7
Mesdopetam hemitartrate ( 1-?Propanamine, N-?[2-?[3-?fluoro-?5-?(methylsulfonyl)?phenoxy]?ethyl]?-?, (2R,?3R)?-?2,?3-?dihydroxybutanedioat?e (2:1) | IRL790 hemitartrate )
产品货号. M28670 CAS No. 2562346-14-7
Mesdopetam hemitartrate 是多巴胺 D3 受体的拮抗剂(Ki=90 nM;对于人重组 D3 受体,IC50=9.8 μM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥464 | 有现货 |
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| 10MG | ¥656 | 有现货 |
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| 25MG | ¥1293 | 有现货 |
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| 50MG | ¥2037 | 有现货 |
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| 100MG | ¥2835 | 有现货 |
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| 200MG | ¥3951 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Mesdopetam hemitartrate
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Mesdopetam hemitartrate 是多巴胺 D3 受体的拮抗剂(Ki=90 nM;对于人重组 D3 受体,IC50=9.8 μM)。
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产品描述Mesdopetam hemitartrate is an antagonist of dopamine D3 receptor (Ki=90 nM; IC50=9.8 μM for human recombinant D3 receptor). It has psychomotor stabilizing properties.
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体外实验——
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体内实验Mesdopetam (IRL790) (3.7, 11, 33, or 100 μmol/kg; s.c.) hemitartrate dose-dependently inhibits the behavioral activation following pretreatment with D-amphetamine or MK-80. Animal Model:Male Sprague-Dawley ratsDosage:3.7, 11, 33, or 100 μmol/kg (synthesized in-house as HCl salt, was dissolved in physiologic saline (0.9% w/v NaCl) Administration:s.c. was administered subcutaneously 4 min before the start of recording Result:Dose-dependently inhibited the behavioral activation following pretreatment with D-amphetamine or MK-801.
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同义词1-?Propanamine, N-?[2-?[3-?fluoro-?5-?(methylsulfonyl)?phenoxy]?ethyl]?-?, (2R,?3R)?-?2,?3-?dihydroxybutanedioat?e (2:1) | IRL790 hemitartrate
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体p38α
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研究领域——
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适应症——
化学信息
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CAS Number2562346-14-7
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分子量700.77
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分子式C28H42F2N2O12S2
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : 100 mg/mL (142.70 mM)
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SMILESCCCNCCOC1=CC(S(=O)(C)=O)=CC(F)=C1.CCCNCCOC2=CC(S(=O)(C)=O)=CC(F)=C2.O=C(O)[C@H](O)[C@@H](O)C(O)=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Baker W, et al. Monophosphates as mutual prodrugs of anti-inflammatory signal transduction modulators (aistm's) and β-agonists for the treatment of pulmonary inflammation and bronchoconstriction. WO 2008076265 A1.
产品手册
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