GSK 356278
CAS No. 720704-34-7
GSK 356278 ( GSK356278;GSK-356278 )
产品货号. M15757 CAS No. 720704-34-7
A potent, selective, brain-penetrant and orally bioavailable phosphodiesterase 4 (PDE4) inhibitor with pIC50 of 8.8 (PDE4B); equally inhibits PDE4A and PDE4Dwith pIC50 of 8.6 and 8.7.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥275 | 有现货 |
|
5MG | ¥446 | 有现货 |
|
10MG | ¥721 | 有现货 |
|
25MG | ¥1401 | 有现货 |
|
50MG | ¥2608 | 有现货 |
|
100MG | ¥4155 | 有现货 |
|
200MG | ¥5654 | 有现货 |
|
500MG | ¥8829 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称GSK 356278
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述A potent, selective, brain-penetrant and orally bioavailable phosphodiesterase 4 (PDE4) inhibitor with pIC50 of 8.8 (PDE4B); equally inhibits PDE4A and PDE4Dwith pIC50 of 8.6 and 8.7.
-
产品描述A potent, selective, brain-penetrant and orally bioavailable phosphodiesterase 4 (PDE4) inhibitor with pIC50 of 8.8 (PDE4B); equally inhibits PDE4A and PDE4Dwith pIC50 of 8.6 and 8.7, exhibits >100-fold selectivity for PDE4B over the other 10 PDEs; inhibits LPS-induced release of TNF-α in human whole blood with pIC50 of 7.6, demonstrates anxiolytic and cognition-enhancing effects without inducing side effects in models of anxiety.Anxiety Phase 1 Clinical
-
同义词GSK356278;GSK-356278
-
通路Angiogenesis
-
靶点PDE
-
受体PDE
-
研究领域Neurological Disease
-
适应症Anxiety
化学信息
-
CAS Number720704-34-7
-
分子量439.54
-
分子式C21H25N7O2S
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCCN1N=CC2=C(NC3CCOCC3)C(C4=NN=C(CC5=C(C)N=C(C)S5)O4)=CN=C21
-
化学全称5-(5-((2,4-dimethylthiazol-5-yl)methyl)-1,3,4-oxadiazol-2-yl)-1-ethyl-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridin-4-amine
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Rutter AR, et al. J Pharmacol Exp Ther. 2014 Jul;350(1):153-63.
2. van der Aart J, et al. J Cereb Blood Flow Metab. 2017 Jan 1:271678X17720868.
2. van der Aart J, et al. J Cereb Blood Flow Metab. 2017 Jan 1:271678X17720868.
产品手册
关联产品
-
BI-409306
BI-409306 is a potent and selective inhibitor of PDE9A (IC50 of 52 nM),and can be used in the research of memory.
-
Ginkgolide J
Ginkgolide J has neuroprotective activity it can prevent A beta(1-42) induced inhibition of long-term potentiation in the CA1 region of mouse hippocampal slices.
-
PF-2545920
PF-2545920 is a potent and selective PDE10A inhibitor with IC50 of 0.37 nM.