上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
PR-104 纯度: 97.71%
PR-104 是一种选择性缺氧激活的 DNA 交联剂,可用于多种异种肿瘤模型的研究。PR-104 作为氮芥的前体药物,可有效地转化为亲脂性较强的二硝基苯甲酰胺芥菜醇 PR-104A。
PR-104 Chemical Structure
CAS No. : 851627-62-8
规格 | 价格 | 是否有货 | 数量 |
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5 mg | ¥4800 | In-stock | |
10 mg | ¥8000 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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PR-104 相关产品
•相关化合物库:
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- Anti-Aging Compound Library
- Drug Repurposing Compound Library
- Covalent Screening Library
- Anti-Lung Cancer Compound Library
生物活性 |
PR-104 is a selective hypoxia-activated DNA cross-linking agent and can be used for the research of multiple tumor xenograft models. PR-104, as a nitrogen mustard pre-prodrug, is converted efficiently to the more lipophilic dinitrobenzamide mustards alcohol PR-104A[1]. |
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体外研究 (In Vitro) |
PR-104 (80 μM; 1 hour; SiHa cells) shows greater suppression of radiation-induced DNA single-strand breaks under hypoxic than aerobic conditions. PR-104 (100 μM; 1 hour; SiHa cells) results in phosphorylation of Ser139 of histone H2AX (gH2AX). PR-104 (0.266 mmol/kg; 18 h; SiHa cells) shows activity against hypoxic cells after irradiation. PR-104 varies in potency between cell lines, with the lowest IC50 (0.51 μmol/L) in H460 cells and highest (7.3 μmol/L) in PC3 prostate cells[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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体内研究 (In Vivo) |
PR-104 (0.56 mmol/kg; i.v. or i.p.; 0~2 hours) makes the plasma area under the curve. PR-104 (0.23 mmol/kg; i.p.; 100 days) shows antitumor activity[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
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Clinical Trial |
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分子量 |
579.27 |
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Formula |
C14H20BrN4O12PS |
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CAS 号 |
851627-62-8 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
-80°C, protect from light, stored under nitrogen |
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溶解性数据 |
In Vitro:
DMSO : 100 mg/mL (172.63 mM; Need ultrasonic) H2O : 31.25 mg/mL (53.95 mM; ultrasonic and warming and heat to 60°C) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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