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1305115-80-3

中文名稱 1305115-80-3
英文名稱 PF 4957325
CAS 1305115-80-3
分子式 C14H15F3N8OS
分子量 400.38
MOL 文件 1305115-80-3.mol
更新日期 2024/11/15 18:20:33
1305115-80-3 結(jié)構(gòu)式 1305115-80-3 結(jié)構(gòu)式

基本信息

中文別名
化合物 T12422
英文別名
PF 4957325
PF 04957325
PF-04957325
PF04957325
PF4957325
3-[[(2R)-4-(1,3-thiazol-2-ylmethyl)morpholin-2-yl]methyl]-5-(trifluoromethyl)triazolo[4,5-d]pyrimidin-7-amine
3H-1,2,3-Triazolo[4,5-d]pyrimidin-7-amine, 3-[[(2R)-4-(2-thiazolylmethyl)-2-morpholinyl]methyl]-5-(trifluoromethyl)-
3-{[(2R)-4-(1,3-thiazol-2-ylmethyl)morpholin-2-yl]methyl}-5-(trifluoromethyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-amine

物理化學(xué)性質(zhì)

密度1.81±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO : 9.9 mg/mL (24.73 mM)
酸度系數(shù)(pKa)4.51±0.10(Predicted)
形態(tài)Solid
顏色White to off-white
1305115-80-3價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08HY-154261305115-80-3
PF-04957325
1305115-80-31mg1500元
2024/11/08HY-154261305115-80-3
PF-04957325
1305115-80-310mM * 1mLin DMSO2643元
2024/11/08HY-154261305115-80-3
PF-04957325
1305115-80-35mg3000元

常見問題列表

生物活性
PF-04957325是一種高效,選擇性的 PDE8 抑制劑,抑制PDE8A和PDE8B的IC50值分別為0.7 nM和0.3 nM。
靶點

IC50: 0.7 nM (PDE8A), less than 0.3 nM (PDE8B)

體外研究

PF-04957325 is over two orders of magnitude less efficient than PICL in suppressing polyclonal Teff cell proliferation, and shows no effect on cytokine gene expression in these cells, despite its robust effect on T cell adhesion. PF-04957325 is a selective PDE8 inhibitor and inhibits breast cancer cell migration. PF-04957325 greatly potentiates steroidogenesis in WT adrenal cells. PF-04957325 shows a reported IC 50 of 0.7 nM against PDE8A, 0.2 nM against PDE8B, and > 1.5 μM against all other PDE isoforms. PF-04957325 treatment of WT Leydig cells or MA10 cells increases steroid production but has no effect in PDE8A (-/-)/B(-/-) double-knockout cells, confirming the selectivity of the drug. Moreover, under basal conditions, cotreatment with PF-04957325 plus rolipram, a PDE4-selective inhibitor, synergistically potentiates steroid production.

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