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- 文献和实验
- 技术资料
- 保存条件:
Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
ML162
- 库存:
999
- 供应商:
北京索莱宝科技有限公司
- CAS号:
1035072-16-2
- 规格:
5mg/1mg/10mg/25mg/50mg
| 规格: | 5mg | 产品价格: | ¥890.00 |
|---|---|---|---|
| 规格: | 1mg | 产品价格: | ¥490.00 |
| 规格: | 10mg | 产品价格: | ¥1440.00 |
| 规格: | 25mg | 产品价格: | ¥2890.00 |
| 规格: | 50mg | 产品价格: | ¥3940.00 |
| CAS | 1035072-16-2 |
| 英文名称 | ML162 |
| 分子式 | C23H22Cl2N2O3S |
| 分子量 | 477.4 |
| 规格 | 5mg ; 1mg ; 10mg ; 25mg ; 50mg |
| 溶解性 | Soluble in DMSO |
| 纯度 | ≥98% |
| 外观(性状) | Off-white to light yellow Solid |
| 储存条件 | Powder:-20℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| 运输条件 | 冷冻运输 |
| EC | 188-421-7 |
| SMILES | COC1=C(C=C(C=C1)N(C(C2=CC=CS2)C(=O)NCCC3=CC=CC=C3)C(=O)CCl)Cl |
| InChIKey | UNVKYJSNMVDZJE-UHFFFAOYSA-N |
| InChI | InChI=1S/C23H22Cl2N2O3S/c1-30-19-10-9-17(14-18(19)25)27(21(28)15-24)22(20-8-5-13-31-20)23(29)26-12-11-16-6-3-2-4-7-16/h2-10,13-14,22H,11-12,15H2,1H3,(H,26,29) |
| PubChem CID | 3689413 |
| 靶点 | GPX4 |
| 通路 | Metabolic Enzyme&Protease |
| 背景说明 | ML162 是一种共价谷胱甘肽过氧化物酶 4 (GPX4) 抑制剂。 |
| 生物活性 | ML162 is a covalent glutathione peroxidase 4 (GPX4) inhibitor. ML162 has a selective lethal effect on mutant RAS oncogene-expressing cell lines[1-2] |
| In Vitro | ML162 (compound 1a) shows nanomolar potencies against two HRASG12V expressing cell lines, with IC50 values of 25 nM and 578 nM for HRASG12V-expressing and wild-type BJ fibroblasts, respectively[1].ML162 induces the head and neck cancer (HNC) cell death to varying degrees, with parental HN3 cells more sensitive and cisplatin-resistant (HN3R) and acquired RSL3-resistant (HN3-rslR) cells less sensitive[2]. |
| 细胞实验 | ML162 (8 μM; 24 hours) treatment increases the expression of p62 and Nrf2 in chemoresistant HN3R and HN3-rslR cells, inactivates Keap1, and increases expression of the phospho-PERK-ATF4-SESN2 pathway[2]. |
| 数据来源文献 | [1]. Michel We?wer, et al. Development of small-molecule probes that selectively kill cells induced to express mutant RAS. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1822-6. [2]. Daiha Shin, et al. Nrf2 inhibition reverses resistance to GPX4 inhibitor-induced ferroptosis in head and neck cancer. Free Radic Biol Med. 2018 Dec;129:454-462. |
| 单位 | 瓶 |
| 表格1 | |*|1mg|5mg|10mg|$$|1mM|2.0947mL|10.4734mL|20.9468mL|$$|5mM|0.4189mL|2.0947mL|4.1894mL|$$|10mM|0.2095mL|1.0473mL|2.0947mL| |


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