TBBD
CAS No. 476-66-4
TBBD ( Ellagic acid )
产品货号. M14590 CAS No. 476-66-4
TBBD 是共激活剂相关精氨酸甲基转移酶 1 (CARM1;PRMT4) 的特异性抑制剂,可选择性抑制组蛋白 H3 (H3R17) 精氨酸 17 的甲基化。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | ¥365 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称TBBD
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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TBBD 是共激活剂相关精氨酸甲基转移酶 1 (CARM1;PRMT4) 的特异性抑制剂,可选择性抑制组蛋白 H3 (H3R17) 精氨酸 17 的甲基化。
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产品描述TBBD is a specific inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1; PRMT4) that selectively inhibits methylation at arginine 17 of histone H3 (H3R17); shows no significant effect on the HMTase activity of G9a, as well as on the HAT activity of p300/CBP-associated factor.(In Vitro):Ellagic acid is a potent CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM. Ellagic acid also blocks other kinases such as LYN, PKA, SYK, GSK3, FGR and CK1, with IC50s of 2.9, 3.5, 4.3, 7.5, 9.4 and 13.0 μM, respectively, and shows no obvious effects on DYRK1a, CSK, NPM-ALK, RET and FLT3 (IC50s > 40 μM). Ellagic acid (5-100 μM) shows inhibitory activities against Karpas299, SUDHL1, SR786, and FE-PD cell lines. Ellagic acid (10 μM) exhibits cytotoxic effects on MCF-7 cells after treatment of radiation. Ellagic acid (10 μM) in combination with Irradiation (IR) significantly abridges the capacity of MCF-7 cells to form colonies equated with individual treatments. Ellagic acid with IR also induces cell apoptosis, and facilitates the upregulation of pro-apopttotic Bax and downregulation of Bcl-2 in MCF-7 cells. (In Vivo):Ellagic acid (EA; 10 mg/kg/day; p.o., 14 days) strongly decreases MDA brain content by 17%, and reduces the levels of brain TNF-α by 42% in rats. Ellagic acid markedly increases the reduced brain contents of 5-HT (39%), dopamine (DA, 71%), and norepinephrine (NE, 77%). Ellagic acid (10 mg/kg, p.o., 14 days) causes decreased histopathological changes induced by Doxorubicin in rats.
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体外实验Ellagic acid is a potent CK2 inhibitor, with an IC50 of 40 nM and a Ki of 20 nM. Ellagic acid also blocks other kinases such as LYN, PKA, SYK, GSK3, FGR and CK1, with IC50s of 2.9, 3.5, 4.3, 7.5, 9.4 and 13.0 μM, respectively, and shows no obvious effects on DYRK1a, CSK, NPM-ALK, RET and FLT3 (IC50s > 40 μM). Ellagic acid (5-100 μM) shows inhibitory activities against Karpas299, SUDHL1, SR786, and FE-PD cell lines. Ellagic acid (10 μM) exhibits cytotoxic effects on MCF-7 cells after treatment of radiation. Ellagic acid (10 μM) in combination with Irradiation (IR) significantly abridges the capacity of MCF-7 cells to form colonies equated with individual treatments. Ellagic acid with IR also induces cell apoptosis, and facilitates the upregulation of pro-apopttotic Bax and downregulation of Bcl-2 in MCF-7 cells.
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体内实验Ellagic acid (EA; 10 mg/kg/day; p.o., 14 days) strongly decreases MDA brain content by 17%, and reduces the levels of brain TNF-α by 42% in rats. Ellagic acid markedly increases the reduced brain contents of 5-HT (39%), dopamine (DA, 71%), and norepinephrine (NE, 77%). Ellagic acid (10 mg/kg, p.o., 14 days) causes decreased histopathological changes induced by Doxorubicin in rats.
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同义词Ellagic acid
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通路Chromatin/Epigenetic
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靶点HMTase
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受体Carbonicanhydrase|CK2|PKA|PKC|Smoothened|Syk
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研究领域Cancer
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适应症——
化学信息
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CAS Number476-66-4
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分子量302.194
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分子式C14H6O8
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纯度>98% (HPLC)
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溶解度Ethanol: 0.2 mg/mL (0.65 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESO=C1C2=CC(O)=C(O)C(O3)=C2C4=C(C3=O)C=C(O)C(O)=C4O1
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化学全称2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione
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. Selvi BR, et al. J Biol Chem. 2010 Mar 5;285(10):7143-52.
2. Hatanaka Y, et al. Cell Rep. 2017 Sep 19;20(12):2756-2765.
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