
KL201
CAS No. 302939-48-6
KL201 ( —— )
产品货号. M28799 CAS No. 302939-48-6
KL201 是一种生物钟调节剂,是一种异构体选择性隐花色素 1 (CRY1) 稳定剂。 KL201 延长细胞和组织的昼夜节律周期。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1604 | 有现货 |
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10MG | ¥3013 | 有现货 |
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25MG | ¥5095 | 有现货 |
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50MG | ¥7258 | 有现货 |
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100MG | ¥9882 | 有现货 |
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200MG | 获取报价 | 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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生物学信息
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产品名称KL201
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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KL201 是一种生物钟调节剂,是一种异构体选择性隐花色素 1 (CRY1) 稳定剂。 KL201 延长细胞和组织的昼夜节律周期。
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产品描述KL201 a circadian clock modulator, is a isoform-selective cryptochrome 1 (CRY1) stabilizer. KL201 lengthens the period of circadian rhythms in cells and tissues.(In Vitro):KL201 causes dose-dependent lengthening of circadian period in Bmal1-dLuc reporter cells, and in cells with another circadian reporter Per2-dLuc. KL201 suppresses the intensity of Per2-dLuc reporter much more than that of Bmal1-dLuc, without affecting cellular viability. KL201 binds to CRY1 in overlap with FBXL3, a subunit of ubiquitin ligase complex, and the effect of KL201 is blunted by knockdown of FBXL3. KL201 lengthened circadian period and suppressed the intensity of Per2::Luc knockin reporter in mouse lung primary explants.
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体外实验KL201 causes dose-dependent lengthening of circadian period in Bmal1-dLuc reporter cells, and in cells with another circadian reporter Per2-dLuc. KL201 suppresses the intensity of Per2-dLuc reporter much more than that of Bmal1-dLuc, without affecting cellular viability.KL201 binds to CRY1 in overlap with FBXL3, a subunit of ubiquitin ligase complex, and the effect of KL201 is blunted by knockdown of FBXL3.KL201 lengthened circadian period and suppressed the intensity of Per2::Luc knockin reporter in mouse lung primary explants.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体hLPA5
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研究领域——
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适应症——
化学信息
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CAS Number302939-48-6
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分子量388.28
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分子式C17H14BrN3OS
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 250 mg/mL (643.87 mM)
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SMILESBrc1ccccc1C(=O)Nc1ncnc2sc3CCCCc3c12
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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.Murai N, et al. Analgesic effects of novel lysophosphatidic acid receptor 5 antagonist AS2717638 in rodents. Neuropharmacology. 2017 Nov;126:97-107.