MLS-573151
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | ¥1935.00 | 现货 | |
| 10mg | ¥3289.00 | 现货 | |
| 25mg | ¥6772.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
MLS-573151 is a specific and cell permeable inhibitor of Cdc42 [1].
Cdc42 is a small GTPase of the Rho family involved in regulating signaling pathways that control diverse cellular functions such as cell morphology, cell migration, cell cycle progression and endocytosis [2].
In vitro: MLS-573151 was a specific, cell permeable inhibitor of Cdc42 with an IC50 of 2 μM [1]. MLS-573151 showed no effect on other GTPases, including the related Rho family members RhoA, Rac1, and Rac2. MLS-573151 functioned by blocking the binding of GTP to Cdc42 [1]. In marrow-derived mesenchymal stem cells, MLS-573151 showed no effect on cell migration [3].
References:
[1] Surviladze Z, Waller A, Wu Y, et al. Identification of a small GTPase inhibitor using a high-throughput flow cytometry bead-based multiplex assay[J]. Journal of biomolecular screening, 2010, 15(1): 10-20.
[2] Qadir M I, Parveen A, Ali M. Cdc42: Role in Cancer Management[J]. Chemical biology & drug design, 2015, 86(4): 432-439.
[3] Wang L, Yang L, Tian L, et al. Cannabinoid Receptor 1 Mediates Homing of Bone Marrow‐Derived Mesenchymal Stem Cells Triggered by Chronic Liver Injury[J]. Journal of cellular physiology, 2017, 232(1): 110-121.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 10179-57-4 |
| 分子式 | C21H19N3O2S |
| 分子量 | 377.5 |
| 化学名称 | 4-(4,5-dihydro-3,5-diphenyl-1H-pyrazol-1-yl)-benzenesulfonamide |
| 溶解度 | ≥42.9 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O |
| SMILES | NS(c(cc1)ccc1N(C(C1)c2ccccc2)N=C1c1ccccc1)(=O)=O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | MLS-573151 (MLS000573151) 是一种选择性 GTPase Cdc42 抑制剂,EC50 为 2 μM。MLS-573151 对 Rab2、Rab7、H-Ras、Rac1、Rac 2 和 RhoA 野生型等其他 GTPase 家族成员无效。MLS-573151 通过阻断 GTP 与 Cdc42 的结合发挥作用。 |



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