(S)-1-tert-Butyl 2-methyl 4-ox
opiperidine-1,2-dicarboxylate 756486-14-3 **科研现货速达** HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等- 询价
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- 文献和实验
- 技术资料
- 英文名：
(S)-1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
756486-14-3
- 规格：
10mg///100mg///200mg
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文献和实验[3H](+)MK801 Radioligand Binding Assay at the N‐Methyl‐D‐Aspartate Receptor
., Siegel, B.W., Harrison, B.L., Gross, R.S., Hawes, C., and Towers, P. 1996. [3H]MDL 105,519, a high‐affinity radioligand for the N‐methyl‐D‐aspartate receptor‐associated glycine recognition site J. Pharmacol. Exp. Ther. 279:62‐68
Activation of SAPKs/JNKs and p38s In Vitro
some of the stimuli known to recruit both the SAPKs/JNKs and p38s. In general, the same stimuli that activate the SAPKs/JNKs will also activate the p38s. One exception is ischemia-reperfusion. In this instance, the SAPKs/JNKs are activated exclusively
can be selectively inhibited by targeting the catalytic site with drug?like compounds. Notably, the mammalian 26S proteasome is associated with three major DUBs: RPN11, UCH37, and USP14. Because the ubiquitin ?chain?trimming? activity of USP14 can inhibit proteasome
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