CAS NO: | 1243244-14-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | LGK974 (WNT974) is an orally bioavailable and specificPorcupine(PORCN) inhibitor with anIC50of 0.1 nM[1]. | ||||||||||||||||
IC50& Target | Porcupine[1] | ||||||||||||||||
体外研究 (In Vitro) | LGK974 effectively displaces [3H]-GNF-1331 with an IC50of 1 nM in the PORCN radioligand binding assay. LGK974 potently reduces Wnt-dependentAXIN2mRNA levels in HN30 cells with an IC50of 0.3 nM[1]. | ||||||||||||||||
体内研究 (In Vivo) | LGK974, a drug that targets Porcupine, a Wnt-specific acyltransferase. LGK974 potently inhibits Wnt signaling, has strong efficacy in rodent tumor models, and is well-tolerated. Toxicology studies are performed on nontumor bearing rats at 3 and 20 mg/kg. At the efficacious dose of 3 mg/kg per day for 14 d, LGK974 is well-tolerated without abnormal histopathological findings in Wnt-dependent tissues, including the intestine, stomach, and skin. When rats are administrated a very high dose of 20 mg/kg per day for 14 d, loss of intestinal epithelium is observed, consistent with the concept that Wnt is required for intestinal tissue homeostasis[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 396.44 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H20N6O | ||||||||||||||||
CAS 号 | 1243244-14-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 32 mg/mL(80.72 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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