Remodelin
CAS No. 949912-58-7
Remodelin( —— )
Catalog No. M16792 CAS No. 949912-58-7
A potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 45 | In Stock |
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10MG | 63 | In Stock |
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25MG | 119 | In Stock |
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50MG | 176 | In Stock |
|
100MG | 259 | In Stock |
|
200MG | 390 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameRemodelin
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NoteResearch use only, not for human use.
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Brief DescriptionA potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules.
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DescriptionA potent inhibitor of the acetyl-transferase protein NAT10 that acetylates both histones and microtubules; significantly reduces the prevalence of misshapen nuclei in HGPS cells, prevents FTI-induced nuclear shape defects in normal fibroblasts and U2OS cells; does not affect Golgi apparatus integrity or tubulin polymer assembly, and does not cause cells to accumulate in mitosis.
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In VitroCell Proliferation Assay Cell Line:Prostate cancer cell lines VCaP, PC3, and DU145Concentration:0,10,20,40 μM Incubation Time:1,2,7 days Result:Inhibited NAT10 and suppressed the growth of both AR-positive and AR-negative prostate cancer cells. Displayed significantly decreased cell proliferation activity over time, compared to the control group.Decreased colony formation ability with a dose-dependent manner. Immunofluorescence Cell Line:Prostate cancer cell lines VCaP, PC3, and DU145 Concentration:0,10,20,40 μM Incubation Time:24 hours Result:Showed a significant decrease in both the positive labeling rate and the fluorescence intensity compared to the control group. Significantly reduced both the staining foci of IdU and the staining foci of CldU compared to control group. Western Blot Analysis Cell Line:Skin fibroblasts from LmnaG609G/G609G and wildtype (WT) littermates Concentration:1 μM Incubation Time:7 days Result:Decreased the higher level of the DNA double-strand break (DSB) marker gamma H2AX (γH2AX, Ser-139 phosphorylated histone H2AX).
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In Vivo——
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Synonyms——
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PathwayCell Cycle/DNA Damage
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TargetHDAC
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RecptorNAT10inhibitor
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number949912-58-7
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Formula Weight282.3635
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Molecular FormulaC15H14N4S
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESC1CCC(=NNC2=NC(=CS2)C3=CC=C(C=C3)C#N)C1
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Chemical NameBenzonitrile, 4-[2-(2-cyclopentylidenehydrazinyl)-4-thiazolyl]-
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. Larrieu D, et al. Science. 2014 May 2;344(6183):527-32.
2. Mathieu J, et al. Cell Stem Cell. 2016 Jul 7;19(1):3-4.
3. Cobb AM, et al. Aging Cell. 2016 Jul 27. doi: 10.1111/acel.12506.
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