ABT 724 trihydrochloride
CAS No. 587870-77-7
ABT 724 trihydrochloride ( —— )
产品货号. M27497 CAS No. 587870-77-7
ABT 724 triHClide 是一种有效的选择性 D4 受体激动剂(EC50 分别 = 12.4 nM、14.3 nM 和 23.2 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥389 | 有现货 |
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| 5MG | ¥648 | 有现货 |
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| 10MG | ¥1037 | 有现货 |
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| 25MG | ¥2130 | 有现货 |
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| 50MG | ¥3426 | 有现货 |
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| 100MG | ¥5095 | 有现货 |
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| 500MG | ¥10935 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称ABT 724 trihydrochloride
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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ABT 724 triHClide 是一种有效的选择性 D4 受体激动剂(EC50 分别 = 12.4 nM、14.3 nM 和 23.2 nM)。
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产品描述ABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies.(In Vitro):A weak affinity to 5-HT1A receptors (Ki = 2780 nM) is observed. ABT 724 trihydrochloride(10 μM) exhibits a selective biochemical profile, as indicated by a lack of binding affinity for >70 neurotransmitter/uptake/ion channels including D2, D3, or D5 receptors. ABT 724 trihydrochloride(10 μM) does not inhibit the PDE activity of PDE1, PDE5, or PDE6.(In Vivo):In male adult Wistar rats, ABT 724 trihydrochloride (8.8 μg/kg; s.c.) treatment facilitated penile erection in a dose-dependent manner.
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体外实验ABT-724 exhibits a selective biochemical profile, as indicates by a lack of binding affinity for >70 neurotransmitter/uptake/ion channels including D2, D3, or D5 receptors up to a 10 μM concentration. A weak affinity to 5-HT1A receptors (Ki = 2780 nM) is observed. ABT-724 does not inhibit the PDE activity of PDE1, PDE5, or PDE6 at 10 μM concentrations.
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体内实验ABT-724 (8.8 μg/kg; subcutaneous injection; daily; for 5 days; male adult Wistar rats) treatment dose-dependently facilitates penile erection when given s.c. to conscious rats. Animal Model:Male adult Wistar rats (~300 g) Dosage:8.8 μg/kg Administration:Subcutaneous injection; daily; for 5 days Result:Dose-dependently facilitated penile erection.
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同义词——
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体M4 mAChR
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研究领域——
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适应症——
化学信息
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CAS Number587870-77-7
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分子量402.7
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分子式C17H22Cl3N5
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : ≥ 100 mg/mL (248.29 mM))
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SMILESC1CN(CCN1CC2=NC3=CC=CC=C3N2)C4=CC=CC=N4.Cl.Cl.Cl
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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.Lei Zhang, et al. 5,7-dihydro-pyrrolo-pyridine derivatives for treating neurological and neurodegenerative diseases. WO2018002760A1
产品手册
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