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Cortivazol 是一种结构独特的吡唑类糖皮质激素受体激动剂,其与受体的结合亲和力比地塞米松高约7.3倍,比泼尼松龙高约165倍。它通过诱导配体结合域的特定构象变化,优先激活糖皮质激素受体而非盐皮质激素受体,从而在白血病细胞系中调控一套不同于地塞米松的专属基因表达谱。在科研中,Cortivazol常被用作分子探针,用以解析糖皮质激素受体的结构-功能关系,并评估细胞周期阻滞与凋亡诱导机制。
别名 Dilaster
Cortivazol 是一种结构独特的吡唑类糖皮质激素受体激动剂,其与受体的结合亲和力比地塞米松高约7.3倍,比泼尼松龙高约165倍。它通过诱导配体结合域的特定构象变化,优先激活糖皮质激素受体而非盐皮质激素受体,从而在白血病细胞系中调控一套不同于地塞米松的专属基因表达谱。在科研中,Cortivazol常被用作分子探针,用以解析糖皮质激素受体的结构-功能关系,并评估细胞周期阻滞与凋亡诱导机制。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | 待询 | 10-14周 | |
| 50 mg | 待询 | 10-14周 | |
| 100 mg | 待询 | 10-14周 |
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| 产品描述 | Cortivazol is a phenylpyrazolosteroid compound that functions as a highly specific agonist for the glucocorticoid receptor, exhibiting negligible activation of the mineralocorticoid receptor. It binds to a distinct region of the ligand binding domain, establishing additional contacts with helices 3 and 5 for a more stable receptor configuration. In comparative studies, cortivazol demonstrates 165-fold greater potency than prednisolone and 7.5-fold higher activity than dexamethasone in cellular assays. This compound is used as a molecular probe to investigate glucocorticoid receptor structure-function relationships, ligand-dependent coactivator recruitment, and the selective regulation of gene expression pathways. |
| 别名 | Dilaster |
| 分子量 | 530.65 |
| 分子式 | C32H38N2O5 |
| CAS No. | 1110-40-3 |
| Smiles | C[C@@]12[C@]([C@]3([C@@]([C@]4(C)C(C(C)=C3)=CC5=C(C4)C=NN5C6=CC=CC=C6)([C@@H](O)C1)[H])[H])(C[C@@H](C)[C@@]2(C(COC(C)=O)=O)O)[H] |
| 密度 | 1.33 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 |
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