CAS NO: | 28097-03-2 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 |
Chaetocin is a specific inhibitor of thehistone methyltransferase(HMT) SU(VAR)3-9 with anIC50of 0.6 μM for SU(VAR)3-9. It also inhibits thioredoxin reductase (TrxR) with anIC50of 4 μM. |
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IC50& Target |
IC50: 0.6 μM (HMT)[1], 4 μM (TrxR)[2] |
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体外研究 (In Vitro) |
Chaetocin is initially isolated from the fermentation broth ofchaetomium minutumand belongs to the class of 3-6 epidithio-diketopiperazines (ETPs). The IC50for SU(VAR)3-9 is 0.6 μM and acts as a competitive inhibitor for S-adenosylmethionine. Chaetocin inhibits the human ortholog of dSU(VAR)3-9 with a similar IC50value of 0.8 μM. It inhibits other known Lys9-specific HMTs such as mouse G9a andNeurospora crassaDIM5 with a higher IC50values of 2.5 and 3 mM, respectively[1]. Chaetocin inhibits TrxR1-initiated turnover of the synthetic substrate DTNB in a cell-free assay in a dose-responsive manner with an IC50of about 4 μM[2].
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体内研究 (In Vivo) |
SL-2 Drosophila tissue cells are cultured in the presence or absence of the inhibitor. Chaetocin has a toxic effect on cells grown in culture. Toxicity is highly dependent on the initial cell density when chaetocin is added to the culture. The number of H3 molecules dimethylated at Lys9 (H3K9me2) is markedly reduced when cells are grown in medium containing 0.5 μM chaetocin after 5 d. Histones isolated from cells treated with 0.1 μM and for a shorter time also shows a drop in Lys9 methylation, but not as strongly as with the higher concentration[1].
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分子量 |
696.84 |
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性状 |
Solid |
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Formula |
C30H28N6O6S4 |
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CAS 号 |
28097-03-2 |
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中文名称 |
毛壳素 |
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结构分类 |
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来源 |
Chaetomium species |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : ≥ 26 mg/mL(37.31 mM) *"≥" means soluble, but saturation unknown.
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In Vivo:
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