ITI214
CAS No. 1642303-38-5
ITI214 ( ITI 214 | ITI-214 )
产品货号. M12494 CAS No. 1642303-38-5
ITI-214 是一种有效的、选择性的、口服活性的磷酸二酯酶 1 (PDE1) 抑制剂,Ki 为 58 pM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1444 | 有现货 |
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| 10MG | ¥2394 | 有现货 |
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| 25MG | ¥4362 | 有现货 |
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| 50MG | ¥6250 | 有现货 |
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| 100MG | ¥8019 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1881 | 有现货 |
|
生物学信息
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产品名称ITI214
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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ITI-214 是一种有效的、选择性的、口服活性的磷酸二酯酶 1 (PDE1) 抑制剂,Ki 为 58 pM。
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产品描述ITI-214 is a potent, selective, orally active phosphodiesterase 1 (PDE1) inhibitor with Ki of 58 pM, displays >1,000-fold selectivity over PDE4A/4D and other PDE isoforms; improves the memory processes of acquisition, consolidation, and retrieval across a broad dose range (0.1-10 mg/kg, po) without disrupting the antipsychotic-like activity of a clinical antipsychotic medication, shows potential for schizophrenia and Alzheimer's disease, movement disorders, attention deficit and hyperactivity disorders, and other central nervous system (CNS) and non-CNS disorders.Parkinson Disease Phase 2 Clinical.
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体外实验——
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体内实验Animal Model:Male Sprague-Dawley rats Dosage:0.1-10 mg/kg Administration:p.o.Result:Significantly enhanced memory performance in the test with a minimum effective dose of 3 mg/kg.
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同义词ITI 214 | ITI-214
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通路Angiogenesis
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靶点PDE
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受体PDE
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研究领域Neurological Disease
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适应症Parkinson Disease
化学信息
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CAS Number1642303-38-5
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分子量605.5566
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分子式C29H29FN7O5P
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 30 mg/mL
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SMILESCN1C(=O)C2=C(N(N=C2N3C1=NC4C3CCC4)CC5=CC=C(C=C5)C6=NC(=CC=C6)F)NC7=CC=CC=C7.OP(=O)(O)O
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化学全称Cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one, 2-[[4-(6-fluoro-2-pyridinyl)phenyl]methyl]-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-, (6aR,9aS)-, phosphate (1:1)
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. Li P, et al. J Med Chem. 2016 Feb 11;59(3):1149-64.
2. Snyder GL, et al. Psychopharmacology (Berl). 2016 Sep;233(17):3113-24.
产品手册
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