CAY10746
CAS No. 2247240-76-0
CAY10746 ( —— )
产品货号. M34824 CAS No. 2247240-76-0
CAY10746 是一种选择性 Rho 激酶 (ROCK) 抑制剂。CAY10746 对 ROCK I、ROCK II 具有抑制活性,IC50 值分别为 0.014 μM 和 0.003 μM。CAY10746 可用于糖尿病视网膜病变(DR)的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥491 | 有现货 |
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| 10MG | ¥785 | 有现货 |
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| 25MG | ¥1776 | 有现货 |
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| 50MG | ¥2492 | 有现货 |
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| 100MG | ¥3249 | 有现货 |
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| 200MG | ¥4383 | 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 | ¥499 | 有现货 |
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生物学信息
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产品名称CAY10746
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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CAY10746 是一种选择性 Rho 激酶 (ROCK) 抑制剂。CAY10746 对 ROCK I、ROCK II 具有抑制活性,IC50 值分别为 0.014 μM 和 0.003 μM。CAY10746 可用于糖尿病视网膜病变(DR)的研究。
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产品描述CAY10746 is a selective Rho kinase (ROCK) inhibitor. CAY10746 has inhibitory activity for ROCK I, ROCK II with IC50 values of 0.014 μM and 0.003 μM, respectively. CAY10746 can be used for the research of diabetic retinopathy (DR).
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体外实验Western Blot Analysis Cell Line:SH-SY5Y cells Concentration:0.1, 1 and 10 μM; 10 μM Incubation Time:2 h; 0.25, 1, 2 and 4 h Result:Inhibited the phosphorylation of MYPT1 but did not impact the MYPT1 expression in dose-dependence and time- dependence.Cell Proliferation Assay Cell Line:SH-SY5Y cells Concentration:1 μM Incubation Time:5 days Result:Significantly protected the cells from death. Cell Migration Assay Cell Line: HUVEC cells Concentration:1 μM Incubation Time:24 h, 36 h Result:Significantly reduced migrating cell numbers and significantly reduce the rate of wound healing at 24 h and 36 h.Apoptosis Analysis Cell Line:ex vivo DR model Concentration:1 μM Incubation Time:5 days Result: Significantly protected neuronal cells from death.
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体内实验——
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同义词——
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通路Cell Cycle/DNA Damage
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靶点ROCK
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受体ROCK
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研究领域——
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适应症——
化学信息
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CAS Number2247240-76-0
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分子量457.48
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分子式C26H23N3O5
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 83.33 mg/mL (182.15 mM; 超声助溶 (<60°C)
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SMILESCN(C)c1ccc(cc1)C(=O)Nc1cccc(NC(=O)COc2ccc3c(c2)occc3=O)c1
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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. Lanying Zhao, et al. Discovery of 4 H-Chromen-4-one Derivatives as a New Class of Selective Rho Kinase (ROCK) Inhibitors, which Showed Potent Activity in ex Vivo Diabetic Retinopathy Models. J Med Chem. 2019 Dec 12;62(23):10691-10710.?
产品手册
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