生物活性
ZCL-278是Cdc42的选择性抑制剂。以Cdc42鸟嘌呤核苷酸交换因子交叉蛋白(ITSN)的结合位点为目标。抑制Cdc42介导的细胞效应，包括3T3成纤维细胞中微峰的形成和初生新生皮质神经元中的神经元分支。还抑制PC3细胞的细胞运动和迁移，无细胞毒性作用。
靶点信息
化学数据
| 目录号 | A13403 |
| 作用机制 | Inhibitor (抑制剂) |
| M. Wt | 584.89 |
| Formula | C21H19BrClN5O4S2 |
| Purity | >99% |
| Storage | Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for36 months.
In solution, store at -20ºC and use within3 monthsto prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles. |
| CAS No. | 587841-73-4 |
| Synonyms | ZCL278, ZCL 278 |
| SMILES | CC1=CC(=NC(=N1)NS(=O)(=O)C2=CC=C(C=C2)NC(=S)NC(=O)COC3=C(C=C(C=C3)Br)Cl)C |
溶解度
| In vitro | DMSO | 99 mg/mL (169.26 mM) |
| Water | Insoluble |
| Ethanol | Insoluble |
*<1 mg/ml means slightly soluble or insoluble.
*Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
储备液配制
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
| 0.1 mM | 17.1 mL | 85.49 mL | 170.97 mL |
| 0.5 mM | 3.42 mL | 17.1 mL | 34.19 mL |
| 1 mM | 1.71 mL | 8.55 mL | 17.1 mL |
| 5 mM | 0.34 mL | 1.71 mL | 3.42 mL |
*The above data is based on the productmolecular weight 584.89. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
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