ErSO
CAS No. 2407860-35-7
ErSO ( —— )
产品货号. M28247 CAS No. 2407860-35-7
ErSO 是通过 ERα 受体选择性激活预期未折叠蛋白反应 (UPR)。 ErSO 可用于抗癌研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2341 | 有现货 |
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| 10MG | ¥3750 | 有现货 |
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| 25MG | ¥6180 | 有现货 |
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| 50MG | ¥8667 | 有现货 |
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| 100MG | ¥11583 | 有现货 |
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| 500MG | ¥23409 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称ErSO
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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ErSO 是通过 ERα 受体选择性激活预期未折叠蛋白反应 (UPR)。 ErSO 可用于抗癌研究。
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产品描述ErSO is a selective activator of anticipatory unfolded protein response (UPR) via ERα receptor. ErSO can be used in studies about anti-cancer.(In Vitro):In MCF-7 cells, ErSO (1-1000 nM) inhibits cell viability with an IC50 of 20.3 nM. ErSO (1 μM) rapidly kills ERα-positive breast cancer cells in TYS and TDG cells and induces rapid killing of ERα-positive MCF-7 human breast cancer cells.(In Vivo):ErSO (10 and 40 mg/kg; p.o.) induces >100000-fold regression (to undetectable amounts) within 14 days and >10000-fold regression of TYS-luciferase-expressing breast tumors in all five mice. In Nu/J mice, ErSO (10 or 40 mg/kg; p.o.) eliminates tumors with >90% reduction in all cases.
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体外实验Cell Viability Assay Cell Line:MCF-7 cells Concentration:1~1000 nM Incubation Time:24 hours Result: Showed that IC50 value is 20.3 nM in MCF-7 cells and inhibited cell viability.
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体内实验Animal Model:Nu/J mice Dosage:10 or 40 mg/kg Administration:P.o.; 21 days Result:Resulted in elimination of these tumors, with >90% reduction in all cases.Animal Model:Mice Dosage:0.5~40 mg/kg Administration:P.o.; 3 weeks Result:Sufficient for a robust response.Animal Model:Mice Dosage:40 mg/kg Administration:I.p.; 14 days Result:Metastatic burden was greatly reduced
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同义词——
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通路Others
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靶点Other Targets
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受体γ secretase
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研究领域——
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适应症——
化学信息
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CAS Number2407860-35-7
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分子量453.33
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分子式C22H13F6NO3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 120 mg/mL (264.71 mM)
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SMILESO=C1[C@@](C=2C(N1)=C(C(F)(F)F)C=CC2)(C3=CC=C(OC(F)(F)F)C=C3)C4=CC=C(O)C=C4
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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.Baumann, et al. Preparation of 4,5,6,7-tetrahydrobenzothiazolyl- or 5,6,7,8-tetrahydroquinazolinylphenylamine derivatives as modulators for amyloid beta. WO2009087127A1
021-51111890
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