assay
≥98% (HPLC)
form
oil
color
colorless to light brown
storage temp.
2-8°C
SMILES string
O=C(CC(C)C)C1=CC=C(OC(F)F)C(OC2CCOC2)=C1
InChI key
IXURVUHDDXFYDR-UHFFFAOYSA-N
Biochem/physiol Actions
Roflupram（FFPM）是有效的抗炎性磷酸二酯酶4（PDE4）抑制剂，可通过增强自噬抑制小胶质细胞炎性体活化。在小胶质细胞BV-2中，roflupram提高了微管相关蛋白1轻链3 Ⅱ（LC3-II）的水平，降低了自噬受体泛素结合蛋白p62（SQSTM1），从而增强自噬、降低炎性体的活化、抑制IL-1β的产生。 发现roflupram（FFPM）可以逆转APP/PS1转基因小鼠的学习和记忆缺陷。
抗炎性磷酸二酯酶4（PDE4）抑制剂
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Hui-Fang Tang et al.
International immunopharmacology, 10(4), 406-411 (2010-01-16)
In the present study, we investigated the effect of classic PDE4 inhibitor rolipram and novel PDE4 inhibitor ZL-n-91 on LPS-induced acute lung injury (ALI) in mice and its mechanism. ALI was induced in ICR mice by instilling intratracheally with LPS
Haibiao Guo et al.
Neuropharmacology, 116, 260-269 (2017-01-10)
Thus far, phosphodiesterase-4 (PDE4) inhibitors have not been approved for application in Alzheimer's disease (AD) in a clinical setting due to severe side effects, such as nausea and vomiting. In this study, we investigated the effect of FFPM, a novel
Shilong Zheng et al.
Journal of medicinal chemistry, 51(24), 7673-7688 (2008-12-04)
Phosphodiesterase 4 catalyzes the hydrolysis of cyclic AMP and is a target for the development of anti-inflammatory agents. We have designed and synthesized a series of phenyl alkyl ketones as PDE4 inhibitors. Among them, 13 compounds were identified as having
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| SML2106-5MG | 04061835502554 |
| SML2106-25MG | 04061835502547 |