N-Methyl-N-[[3-(4-Pyridinyl)Phenyl]Methyl]-4’-(Aminocarbonyl)[1,1’-Biphenyl]-4-Yl Carbamic Acid Ester N-甲基-N-[[3-（4-吡啶基）苯基]甲基]-4’-（氨基羰基）[1,1’-联苯]-4-基氨基甲酸酯
CAS 947669-91-2 MFCD047669912
化学结构图
SMILES:
化学属性
| Mol. Formula | C27H23N3O3 |
|---|
别名和识别编码
| Chemical Name | N-Methyl-N-[[3-(4-Pyridinyl)Phenyl]Methyl]-4’-(Aminocarbonyl)[1,1’-Biphenyl]-4-Yl Carbamic Acid Ester |
|---|---|
| Chemicalbook ID | CB22454225 |
| Chemical Name Translation | N-甲基-N-[[3-（4-吡啶基）苯基]甲基]-4’-（氨基羰基）[1,1’-联苯]-4-基氨基甲酸酯 |
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相关文献及参考
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- [3]. Tchantchou F, et al. Selective inhibition of alpha/beta-hydrolase domain 6 attenuates neurodegeneration, alleviates blood brain barrier breakdown, and improves functional recovery in a mouse model of traumatic brain injury. J Neurotrauma. 2013 Apr 1;30(7):565-79.
- [1]. Li W, et al. A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases. J Am Chem Soc. 2007 Aug 8;129(31):9594-5.
- [1]. Li W, et al. A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases. J Am Chem Soc. 2007 Aug 8;129(31):9594-5.
- [2]. Tanaka M, et al. WWL70 attenuates PGE2 production derived from 2-arachidonoylglycerol in microglia by ABHD6-independent mechanism. J Neuroinflammation. 2017 Jan 10;14(1):7.
- [3]. Tchantchou F, et al. Sele
