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生物源
synthetic (organic)
品質等級
化驗
≥95%
形狀
solid
溶解度
methanol: 10 mg/mL, clear, orange to red
儲存溫度
2-8°C
SMILES 字串
Cl.CN(C)CCCn1cc(C2=C(C(=O)NC2=O)c3c[nH]c4ccccc34)c5ccccc15
InChI
1S/C25H24N4O2.ClH/c1-28(2)12-7-13-29-15-19(17-9-4-6-11-21(17)29)23-22(24(30)27-25(23)31)18-14-26-20-10-5-3-8-16(18)20;/h3-6,8-11,14-15,26H,7,12-13H2,1-2H3,(H,27,30,31);1H
InChI 密鑰
XRAMWNCMYJHGGH-UHFFFAOYSA-N
一般說明
GF 109203X可防止胶原蛋白触发的腺苷和三磷酸(ATP)分泌。它还可抑制胶原蛋白和α-凝血酶诱导的血小板聚集。它可作为糖原合成酶激酶-3(GSK-3)的抑制剂。GF 109203X也可作为一种抗炎剂。
應用
GF 109203X盐酸盐已被用于在人神经母细胞瘤衍生的kelly细胞中抑制蛋白激酶C。
生化/生理作用
蛋白激酶C的抑制剂;GSK-3的有效抑制剂。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Anti-inflammatory properties of the protein kinase C inhibitor, 3-[1-[3-(dimethylamino) propyl]-1H-indol-3-yl]-4 (1H-indol-3-yl)-1H-pyrrole-2, 5-dione monohydrochloride (GF109203X) in the PMA-mouse ear edema model
Agents and Actions, 39(1), C169-C173 (1993)
The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C
The Journal of Biological Chemistry, 266(24), 15771-15781 (1991)
Phorbol-ester mediated suppression of hASH1 synthesis: multiple ways to keep the level down
Frontiers in Molecular Neuroscience, 4(1), 1-1 (2011)
The protein kinase C inhibitors bisindolylmaleimide I (GF 109203x) and IX (Ro 31-8220) are potent inhibitors of glycogen synthase kinase-3 activity
Febs Letters, 460(3), 433-436 (1999)
Experimental cell research, 315(1), 39-49 (2008-10-28)
p120-catenin (p120) is required for cadherin stability and is thought to have a central role in modulating cell-cell adhesion. Several lines of evidence suggest that S/T phosphorylation may regulate p120 activity, but the upstream kinases involved have not been established
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