Chemical Structure : LXQ-87
货号: PC-27109Not For Human Use, Lab Use Only.
LXQ-87 is a selective, orally active, allosteric inhibitor of protein tyrosine phosphatase 1B (PTP1B/PTPN1) with IC50 of 1.06 uM, displays excellent selectivity over TCPTP and SHP-2.
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LXQ-87 is a selective, orally active, allosteric inhibitor of protein tyrosine phosphatase 1B (PTP1B/PTPN1) with IC50 of 1.06 uM, displays excellent selectivity over TCPTP and SHP-2.
educes the fasting blood glucose level and improves glucose tolerance and dyslipidemia in BKS db/db mice suffering from T2DM.
LXQ-87 alleviates insulin resistance and promotes cellular glucose uptake by directly binding to intracellular PTP1B.
LXQ-87 exhibits potent antiproliferative effects across a range of cancer cell lines.
LXQ-87 initiates intrinsic mitochondrial apoptosis, causes G0/G1 phase arrest through decreased Cyclin D1/CDK4/6/c-Myc expression, curbs cell migration, and raises reactive oxygen species (ROS) levels, LXQ-87 also reduces STAT3 phosphorylation.
| 分子量 | 534.20 | |
| 分子式 | C23H18Br2O5 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Gao C, et al. Eur J Med Chem. 2025 Jan 15;282:117053.
2. Xu F, et al. Bioorg Chem. 2026 Jun 18;180:110127.
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