溶解性 | DMSO 5 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
存贮条件 | 储存温度-20°C |
应用 | A highly potent and selective inhibitor of phosphodiesterase 4 |
产品介绍 | GSK256066是PDE4B抑制剂,IC50为3.2 pM,与A-D各亚型亲和力相同,比对PDE1/2/3/5/6和PDE7的抑制性高380000倍和2500倍。 |
生化机理 | GSK256066 is a slow and tight binding inhibitor of PDE4B with apparent IC50 of 3.2 pM. GSK256066 is an extremely potent inhibitor of LPS-stimulated TNFα production in PBMCs with pIC50 of 11.0 and IC50 of 10 pM and human whole-blood cultures with pIC50 of 9.90 and IC50 of 126 pM. GSK256066 is highly selective for PDE4 (>3.8 × 105-fold versus PDE1, PDE2, PDE3, PDE5, and PDE6 and >2.5 × 103-fold against PDE7). GSK256066 inhibits PDE4 isoforms A-D with equal affinity. |
别名 | GSK-256066;GSK 256066; 6-[[3-[(二甲基氨基)羰基]苯基]磺酰]-4-[(3-甲氧基苯基)氨基]-8-甲基-3-喹啉甲酰胺;GSK-256066;GSK 256066; 6-[[3-[(Dimethylamino)carbonyl]phenyl]sulfonyl]-4-[(3-methoxyphenyl)amino]-8-methyl-3-quinolinecarboxamide |
GSK256066
GSK256066 (订货以英文为准)
编号:G127379
CAS号:801312-28-7
分子式:C27H26N4O5S
分子量:518.58
产品名称 | GSK256066 |
中文名称 | GSK256066 |
CAS号 | 801312-28-7 |
分子式(M.F.) | C27H26N4O5S |
分子量(M.W.) | 518.58 |
储存条件 | -20°C储存 |
搜索质检报告(COA)
搜索MSDS
相关产品