D 159687
CAS No. 1155877-97-6
D 159687 ( —— )
产品货号. M20211 CAS No. 1155877-97-6
D159687 是一种选择性 PDE4D 抑制剂,具有良好的认知功能,因为它可以改善新物体识别测试中的记忆力,但没有抗抑郁或抗焦虑作用。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥282 | 有现货 |
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| 10MG | ¥451 | 有现货 |
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| 25MG | ¥930 | 有现货 |
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| 50MG | ¥1488 | 有现货 |
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| 100MG | ¥2151 | 有现货 |
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| 200MG | ¥3051 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥312 | 有现货 |
|
生物学信息
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产品名称D 159687
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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D159687 是一种选择性 PDE4D 抑制剂,具有良好的认知功能,因为它可以改善新物体识别测试中的记忆力,但没有抗抑郁或抗焦虑作用。
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产品描述D159687 is a selective?PDE4D?inhibitorhad a procognitive profile as it improved memory in the novel object recognition test but had no antidepressant or anxiolytic benefit.
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体外实验D159687 (1 μM, 0-24?hours) induces a transient increase in CREB phosphorylation which peaked at 6?hours after treatment.D159687 (0.01-1 μM, 6 hours) causes optimal CREB phosphorylation at 1?μM.Western Blot Analysis Cell Line:HT-22 (mouse hippocampal cell line)Concentration:1 μM Incubation Time: 0, 1, 3, 6, 12, 24?hours Result:Induced a transient increase in CREB phosphorylation which peaked at 6?hours after treatment. Western Blot Analysis Cell Line:HT-22 (mouse hippocampal cell line)Concentration:0.01 μM, 0.1 μM, 1 μM Incubation Time:6 hours Result:CREB phosphorylation was optimal at 1?μM.
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体内实验D159687 (0.05-5 mg/kg; oral daily for a week) shows a potential recruitment or enhancement of synaptic function with increased task difficulty in female Cynomolgus macaques. Animal Model:Female Cynomolgus macaques (4–6 year old) Dosage:0.05, 0.5, 5 mg/kg Administration:Oral daily for a week Result:A potential recruitment or enhancement of synaptic function with increased task difficulty.
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同义词——
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通路Angiogenesis
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靶点PDE
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受体PDE4D
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研究领域——
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适应症——
化学信息
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CAS Number1155877-97-6
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分子量366.85
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分子式C21H19ClN2O2
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纯度>98% (HPLC)
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溶解度DMSO:150 mg/mL?(408.90 mM)
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SMILESCOc1ccc(Cc2ccc(NC(N)=O)cc2)cc1-c1cccc(Cl)c1
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化学全称[4-[[3-(3-Chlorophenyl)-4-methoxyphenyl]methyl]phenyl]urea
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.Zhang C et al. Comparison of the Pharmacological Profiles of Selective PDE4B and PDE4D Inhibitors in the Central Nervous System. Sci Rep. 2017 Jan 5;7:40115.
产品手册
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