TM6089 是一种独特的 PHD 抑制剂，可刺激 HIF 活性而不会产生铁螯合作用，诱导血管生成并对缺血器官发挥保护作用。 TM6089 局部施用可增强血管生成，并且口服施用在表达缺氧反应的报告载体的转基因大鼠中刺激 HIF 活性。
CAS：863421-32-3
分子式：C13H14N4O3S
分子量：306.34
纯度：98%
存储：Store at -20°C

Background:

TM6089 is a unique Prolyl Hydroxylase (PHD) inhibitor which stimulates HIF activity without iron chelation and induces angiogenesis and exerts organ protection against ischemia. Local administration of TM6089 enhances angiogenesis, and oral administration stimulates HIF activity in transgenic rats expressing a hypoxia-responsive reporter vector[1].

[1]. Nangaku M, et al. A novel class of prolyl hydroxylase inhibitors induces angiogenesis and exerts organ protection against ischemia. Arterioscler Thromb Vasc Biol. 2007 Dec;27(12):2548-54.