
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥389 | 有现货 |
![]() ![]() |
5MG | ¥648 | 有现货 |
![]() ![]() |
10MG | ¥915 | 有现货 |
![]() ![]() |
25MG | ¥1839 | 有现货 |
![]() ![]() |
50MG | ¥3467 | 有现货 |
![]() ![]() |
100MG | ¥5176 | 有现货 |
![]() ![]() |
500MG | ¥11097 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Mesdopetam hemitartrate
-
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
-
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)。
-
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.
-
体外实验——
-
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.
-
同义词1-?Propanamine, N-?[2-?[3-?fluoro-?5-?(methylsulfonyl)?phenoxy]?ethyl]?-?, (2R,?3R)?-?2,?3-?dihydroxybutanedioat?e (2:1) | IRL790 hemitartrate
-
通路GPCR/G Protein
-
靶点Dopamine Receptor
-
受体p38α
-
研究领域——
-
适应症——
化学信息
-
CAS Number2562346-14-7
-
分子量700.77
-
分子式C28H42F2N2O12S2
-
纯度>98% (HPLC)
-
溶解度In Vitro:?H2O : 100 mg/mL (142.70 mM)
-
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
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
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




关联产品
-
rac-Rotigotine hydro...
多巴胺 D3 受体的非选择性激动剂 (Ki=0.71 nM);对 D3 受体的选择性是 D2、D4 和 D5 受体的 10 倍,对 D3 受体的选择性是 D1 受体的 100 倍。
-
Dehydroevodiamine
脱氢吴茱萸碱是吴茱萸的一种成分,具有多种生物效应,如降血压、负变时、离子通道抑制剂、抑制一氧化氮产生和增强脑血流活性。
-
Centanafadine hydroc...
盐酸 Centanafadine 是去甲肾上腺素 (NE)/多巴胺 (DA) 转运蛋白的双重抑制剂。