
KL201
CAS No. 302939-48-6
KL201( —— )
Catalog No. M28799 CAS No. 302939-48-6
KL201 a circadian clock modulator, is a isoform-selective cryptochrome 1 (CRY1) stabilizer. KL201 lengthens the period of circadian rhythms in cells and tissues.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 178 | Get Quote |
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10MG | 335 | Get Quote |
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25MG | 566 | Get Quote |
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50MG | 806 | Get Quote |
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100MG | 1098 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameKL201
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NoteResearch use only, not for human use.
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Brief DescriptionKL201 a circadian clock modulator, is a isoform-selective cryptochrome 1 (CRY1) stabilizer. KL201 lengthens the period of circadian rhythms in cells and tissues.
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DescriptionKL201 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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In VitroKL201 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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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorhLPA5
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Research Area——
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Indication——
Chemical Information
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CAS Number302939-48-6
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Formula Weight388.28
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Molecular FormulaC17H14BrN3OS
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (643.87 mM)
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SMILESBrc1ccccc1C(=O)Nc1ncnc2sc3CCCCc3c12
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Murai N, et al. Analgesic effects of novel lysophosphatidic acid receptor 5 antagonist AS2717638 in rodents. Neuropharmacology. 2017 Nov;126:97-107.
molnova catalog



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