Chemical Structure : P-50429
CAS No.: 1247825-37-1
货号: PC-43555Not For Human Use, Lab Use Only.
P-50429 (P50429, P 50429) is a potent, selective, covalent deubiquitinase USP7 (EC50=0.42 uM)/USP47 (EC50=1.0 uM) inhibitor with no inhibition for caspase 3, calpain 1, 20S proteasome and a panel of representative USPs.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥1280 | In stock | |
10 mg | ¥1980 | In stock | |
25 mg | ¥3280 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
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P-50429 (P50429, P 50429) is a potent, selective, covalent deubiquitinase USP7 (EC50=0.42 uM)/USP47 (EC50=1.0 uM) inhibitor with no inhibition for caspase 3, calpain 1, 20S proteasome and a panel of representative USPs.
P-50429 exhibits 20-fold more potent inhibition of USP7 compared with P22077 (IC50 0.42 versus 8.0 uM).
P-50429 destabilizes HDM2, increases p53 and the downstream target p21, inhibits the proliferation of HCT-116 cells.
分子量 | 484.3992 | |
分子式 | C18H11Cl2N3O3S3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 44 mg/mL |
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Chemical Name/SMILES |
2-Thiophenecarboxamide, 4-cyano-5-[(3,5-dichloro-4-pyridinyl)thio]-N-[4-(methylsulfonyl)phenyl]- |
1. Weinstock J, et al. ACS Med Chem Lett. 2012 Sep 11;3(10):789-92.
2. Pozhidaeva A, et al. Cell Chem Biol. 2017 Oct 4. pii: S2451-9456(17)30330-6.
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