SDZ281-977
CAS No. 150779-71-8
SDZ281-977 ( —— )
产品货号. M33494 CAS No. 150779-71-8
SDZ 281-977 是 EGF 受体酪氨酸激酶抑制剂 Lavendustin A 的衍生物。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2356 | 有现货 |
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| 10MG | ¥3772 | 有现货 |
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| 25MG | ¥5933 | 有现货 |
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| 500MG | 获取报价 | 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 | ¥2594 | 有现货 |
|
生物学信息
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产品名称SDZ281-977
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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SDZ 281-977 是 EGF 受体酪氨酸激酶抑制剂 Lavendustin A 的衍生物。
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产品描述SDZ 281-977 is a derivative of the EGF receptor tyrosine kinase inhibitor Lavendustin A.
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体外实验The anticancer profile of SDZ 281-977 is investigated in nude mice bearing the human tumor cell lines A431 (vulvar carcinoma cells), MIA PaCa-2 (pancreatic tumor cells) and MDA-MB-231 (breast carcinoma cells). These cell lines are selected because of their sensitivity for SDZ 281-977. The IC50 values for inhibition of growth of A431, MIA PaCa-2 and MDA-MB-231 cells are 0.21 μM, 0.29 μM and 0.43 μM, respectively.
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体内实验Nude mice bearing A431 human vulvar carcinomas receive intravenous injections of SDZ 281-977 (1-10 mg/kg) for 4 weeks. This treatment results in a dose-dependent inhibition of tumor growth. Orally administered SDZ 281-977 (30 mg/kg) induces a 54% inhibition of A431 tumor growth after 3 weeks of treatment. The above regimens are well tolerated. No significant change in body weight occurred during treatment.
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同义词——
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通路Angiogenesis
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靶点EGFR
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受体EGFR
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研究领域——
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适应症——
化学信息
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CAS Number150779-71-8
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分子量316.35
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分子式C18H20O5
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (316.11 mM; 超声助溶 )
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SMILESCOC(=O)c1cc(CCc2cc(OC)ccc2OC)ccc1O
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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. Cammisuli S, et al. SDZ 281-977: a modified partial structure of lavendustin A that exerts potent and selective antiproliferative activities in vitro and in vivo. Int J Cancer. 1996 Jan 26;65(3):351-9.?
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