DMU-212
CAS No. 134029-62-2
DMU-212 ( —— )
产品货号. M28078 CAS No. 134029-62-2
DMU-212 是白藜芦醇的甲基化形式,具有抗有丝分裂、抗增殖和抗氧化活性。 DMU-212 通过激活 ERK1/2 蛋白并促进细胞凋亡来诱导有丝分裂停滞。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥278 | 有现货 |
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| 5MG | ¥487 | 有现货 |
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| 10MG | ¥749 | 有现货 |
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| 25MG | ¥1479 | 有现货 |
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| 50MG | ¥2539 | 有现货 |
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| 100MG | ¥3591 | 有现货 |
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| 500MG | ¥7641 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥432 | 有现货 |
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生物学信息
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产品名称DMU-212
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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DMU-212 是白藜芦醇的甲基化形式,具有抗有丝分裂、抗增殖和抗氧化活性。 DMU-212 通过激活 ERK1/2 蛋白并促进细胞凋亡来诱导有丝分裂停滞。
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产品描述DMU-212, a methylated form of Resveratrol, shows antimitotic, antiproliferative, and antioxidant activities. DMU-212 induces mitotic arrest through the activation of ERK1/2 protein and the promotion of apoptosis.(In Vitro):DMU-212 (0.3125-40 μM) inhibited the cellular proliferation of human melanoma cells at submicromolar or micromolar concentrations (IC50=0.5 μM, 0.5 μM, 1.25 μM, and 1.25 μM for A375, Bro, MeWo, and M5 human melanoma cells, respectively.).(In Vivo):In SCID female mice, DMU-212 (50 mg/kg; i.g.) inhibited tumor growth and lowered tumor burden.
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体外实验Cell Proliferation Assay Cell Line:A375 cells, MeWo cells, M5 cells, Bro cells Concentration:0.3125 μM, 0,625 μM, 1.25 μM, 2.5 μM, 5 μM, 10 μM, 20 μM, 40 μM Incubation Time:96 hours Result:Inhibited the cellular proliferation of human melanoma cells at submicromolar or micromolar concentrations (IC50=0.5 μM for A375 and Bro and IC50= 1.25 μM for MeWo and M5 cells).Cell Cycle Analysis Cell Line:A375 cells Concentration:20 μM, 30 μM, 50 μM Incubation Time:24 hoursResult:Caused a marked increase in the levels of p21, p53 and cyclin B1 proteins with a concomitant decrease in the levels of cyclin A2.Western Blot Analysis Cell Line:A375 cells Concentration:20 μM, 30 μM, 50 μM Incubation Time:24 hours Result:Significant upregulated Bax, caspase 3 and caspase 9 protein levels, while decreased the levels of the anti-apoptotic protein Bcl-2.Apoptosis Analysis Cell Line:A375 cells Concentration:10 μM, 20 μM Incubation Time:24 hours, 36 hoursResult:Induced apoptosis.
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体内实验Animal Model:6-weeks-old SCID female mice (20-24 g), with ovarian cancer xenografts Dosage:50 mg/kg Administration:Oral gavage, three times a week, for 14 days Result:Lowered tumor burden.
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同义词——
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通路Apoptosis
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靶点Apoptosis
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受体Tubulin polymerization
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研究领域——
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适应症——
化学信息
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CAS Number134029-62-2
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分子量300.35
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分子式C18H20O4
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 20 mg/mL (66.59 mM)
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SMILESCOC1=CC=C(/C=C/C2=CC(OC)=C(OC)C(OC)=C2)C=C1
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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.Schneider Y, et al. Resveratrol analog (Z)-3,5,4'-trimethoxystilbene is a potent anti-mitotic drug inhibiting tubulin polymerization. Int J Cancer. 2003 Nov 1;107(2):189-96.
产品手册
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