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Daminozide (Synonyms: 丁酰肼) 纯度: ≥98.0%
Daminozide 是一种植物生长调节剂,是人类 KDM2/7 组蛋白脱甲基酶的选择性抑制剂,对 PHF8,KDM2A 和 KIAA1718 的 IC50 值分别为 0.55,1.5 和 2.1 μM。与测试的其他脱甲基酶亚家族成员相比,Daminozide 对 KDM2/7 亚家族具有 >100倍的选择性。
Daminozide Chemical Structure
CAS No. : 1596-84-5
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10 mM * 1 mL in DMSO | ¥500 | In-stock | |
500 mg | ¥400 | In-stock | |
1 g | ¥500 | In-stock | |
5 g | ¥800 | In-stock | |
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Daminozide 相关产品
•相关化合物库:
- Bioactive Compound Library Plus
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- Anti-Cancer Compound Library
- FDA Approved & Pharmacopeial Drug Library
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- Targeted Diversity Library
- Tumorigenesis Related Compound Library
生物活性 |
Daminozide, a plant growth regulator, is a selective inhibitor of the human KDM2/7 histone demethylases, with IC50s of 0.55, 1.5 and 2.1 μM for PHF8, KDM2A, and KIAA1718, respectively. Daminozide has >100-fold selectivity for KDM2/7 subfamily versus other demethylase subfamily members tested[1][2]. |
IC50 & Target |
IC50: 0.55 μM (PHF8), 1.5 μM (KDM2A), 2.1 μM (KIAA1718)[1] |
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体外研究 (In Vitro) |
Daminozide has >100-fold selectivity for KDM2/7 subfamily versus other demethylase subfamily members tested (IC50=127 μM for KDM3A, or greater against other demethylases)[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) |
Daminozide (200-20000 ppm) has teratogenic and genotoxic effects on model organism Drosophila melanogaster[2]. 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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分子量 |
160.17 |
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Formula |
C6H12N2O3 |
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CAS 号 |
1596-84-5 |
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中文名称 |
丁酰肼 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 106.67 mg/mL (665.98 mM; Need warming) H2O : 100 mg/mL (624.34 mM; Need ultrasonic) 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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