Chemical Structure : KP-457
CAS No.: 1365803-52-6
货号: PC-25875Not For Human Use, Lab Use Only.
KP-457 is a potent, selective ADAM17 inhibitor with IC50 of 11.1 nM, >50 times more selective for ADAM17 than for other MMPs and ADAM10.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥1780 | In stock | |
| 10 mg | ¥2880 | In stock | |
| 25 mg | ¥4980 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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KP-457 is a potent, selective ADAM17 inhibitor with IC50 of 11.1 nM, >50 times more selective for ADAM17 than for other MMPs and ADAM10.
KP-457 blocks Zn2+ chelation of the catalytic domain of ADAM17.
KP‐457 blocks GPIbα shedding from iPSC platelets at a lower half‐maximal inhibitory concentration than panmetalloproteinase inhibitor GM‐6001.
KP‐457 exhibits improved GPIbα‐dependent aggregation not inferior to human fresh platelets.
KP-457 effectively enhances the production of functional human iPSC‐derived platelets at 37°C.
| 分子量 | 480.55 | |
| 分子式 | C21H24N2O7S2 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
N-(2-((4-(But-2-yn-1-yloxy)phenyl)sulfonyl)-1-(4-(methylsulfonamidomethyl)phenyl)ethyl)-N-hydroxyformamide |
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1. Hirata S, et al. Stem Cells Transl Med. 2017 Mar;6(3):720-730.
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