5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮
生物活性体外研究体内研究靶点 用途与合成方法 MSDS 5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮价格(试剂级) 上下游产品信息
中文名称 | 5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 |
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中文同义词 | 5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 2MG;5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮;PI3KΓ抑制剂(AS-252424);化合物AS-252424;(5Z)-5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮;AS-252424,PI3KΓ抑制剂 |
英文名称 | 5-[[5-(4-Fluoro-2-hydroxyphenyl)-2-furanyl]methylene]-2,4-thiazolidinedione |
英文同义词 | 5-[[5-(4-Fluoro-2-hydroxyphenyl)-2-furanyl]methylene]-2,4-thiazolidinedione;AS-252424;(E)-5-((5-(4-fluoro-2-hydroxyphenyl)furan-2-yl)Methylene)thiazolidine-2,4-dione;(Z)-5-((5-(4-fluoro-2-hydroxyphenyl)furan-2-yl)methylene)thiazolidine-2,4-dione;AS 252424 5-[[5-(4-Fluoro-2-hydroxyphenyl)-2-furanyl]methylene]-2,4-thiazolidinedione;AS-252424;AS 252424;(5Z)-5-[[5-(4-Fluoro-2-hydroxyphenyl)-2-furanyl]methylene]-2,4-thiazolidinedione;CS-182 |
CAS号 | 900515-16-4 |
分子式 | C14H8FNO4S |
分子量 | 305.28 |
EINECS号 | |
相关类别 | 信号转导通路激酶抑制剂;小分子抑制剂,天然产物;细胞生物学试剂;Inhibitors;Akt;mTOR;PI3K;Phosphoinositide 3-kinase PI3-kinase p110γ inhibitor.;A phosphoinositide 3-kinase PI3-kinase p110γ inhibitor. |
Mol文件 | 900515-16-4.mol |
结构式 |
5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 性质
熔点 | >235oC (dec.) |
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密度 | 1.559±0.06 g/cm3(Predicted) |
储存条件 | 2-8°C |
溶解度 | 二甲基亚砜:>20mg/mL |
形态 | 固体 |
酸度系数(pKa) | 7.20±0.20(Predicted) |
颜色 | 粘黄色 |
5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 用途与合成方法
生物活性
AS-252424是一种新型,有效的PI3Kγ抑制剂,IC50为30 nM,作用于PI3Kγ比作用于PI3Kα选择性高30倍,对PI3Kδ/β具有低的抑制活性。
体外研究
AS-252424 is a furan-2-ylmethylene thiazolidinedione as a selective ATP-competitive PI3Kγ inhibitor with IC50 with 33 nM. AS-252424 shows reduced potency on PI3Kα with an IC50 with 935 nM. When screening against 80 different Ser/Thr and Tyr kinases, AS-252424 doesn't show significant inhibit towards any of them at 10 μM except for CK2. AS-252424 inhibits C5a-mediated PKB/Akt phosphorylation in a concentration- dependent manner with submicromolar or low-micromolar IC50 value. AS-252424 inhibits MCP-1-mediated chemotaxis in wild-type primary monocytes in a concentration-dependent manner with an IC50 value of 52 μM, as well as in the monocytic cell line THP-1 with an IC50 value of 53 μM. AS252424 specifically blocks proliferation in the pancreatic cancer cell lines HPAF and Capan1, as assessed by cell counting. A recent research indicates 100 nM of AS-252424 significantly reduces [Ca2+]i, ICa and Ca2+ transients in HL-1 cardiomyocytes.
体内研究
Oral administration of AS-252424 at 10 mg/kg results in moderate reduction of neutrophil recruitment (35%), almost matching the result observed in PI3Kγ-deficient mice.
靶点
PI3Kα 935 nM (IC 50) | PI3Kγ 30 nM (IC 50) | PI3Kδ 20 μM (IC 50) | PI3Kβ 20 μM (IC 50) |
安全信息
WGK Germany | 3 |
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MSDS信息
5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/08/19 | HY-13532 | AS-252424 | 1 mg | 350元 | |
2024/08/19 | HY-13532 | 5-[[5-(4-氟-2-羟基苯基)-2-呋喃基]亚甲基]-2,4-噻唑烷二酮 AS-252424 | 900515-16-4 | 5mg | 770元 |