Chemical Structure : LFHP-1c
货号: PC-23800Not For Human Use, Lab Use Only.
LFHP-1c is a direct phosphoglycerate mutase family member 5 (PGAM5) inhibitor with binding SPR KD of 961 nM, not only inhibits the PGAM5 phosphatase activity, but also reduces the interaction of PGAM5 with NRF2.
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LFHP-1c is a direct phosphoglycerate mutase family member 5 (PGAM5) inhibitor with binding SPR KD of 961 nM, not only inhibits the PGAM5 phosphatase activity, but also reduces the interaction of PGAM5 with NRF2.
LFHP-1c dose-dependently protects rat brains against ischemia/reperfusion injury.
LFHP-1c prevents BBB disruption and attenuates endothelial inflammation in rat cerebral microvessels.
LFHP-1c prevents brain microvascular endothelial cells injury under OGD/R condition.
LFHP-1c targets PGAM5 to facilitate nuclear translocation of NRF2 for endothelial protection in stroke.
LFHP-1c ameliorates brain ischemic injury in tMCAO model of M. fascicularis through PGAM5–NRF2 axis.
分子量 | 873.16 | |
分子式 | C55H64N6O4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Gao C, et al. Acta Pharm Sin B. 2021 Jul;11(7):1867-1884.
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