计算溶液所需的质量、体积或浓度。
活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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G129390-1mg |
1mg |
现货 ![]() |
| |
G129390-5mg |
5mg |
期货 ![]() |
| |
G129390-10mg |
10mg |
现货 ![]() |
| |
G129390-50mg |
50mg |
现货 ![]() |
|
英文别名 | NCGC00024760-07 | Go 6850 | KBio2_003068 | Bio2_000900 | Bisindolylmaleimide I (GF 109203X) | MFCD00236428 | AKOS024458625 | SCHEMBL338086 | 3-{1-[3-(DIMETHYLAMINO)PROPYL]-1H-INDOL-3-YL}-4-(1H-INDOL-3-YL)-1H-PYRROLE-2,5-DIONE | IDI1_002175 | 1H-Pyrrole-2, |
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规格或纯度 | Moligand™, ≥99% |
英文名称 | GF109203X |
生化机理 | Bisindolylmaleimide I(GF 109203X)是一种受石硫合剂启发的分子,已被证明对所有已知的 PKC 异构体(IC50 = 8-20 nM)具有同样有效的抑制作用,但选择性更强。抑制作用对 ATP 具有竞争性,这证明 Bisindolylmaleimide I 能占据 PKC 异构体的 ATP 结合域。双吲哚马来酰亚胺 I(GF 109203X)已被用于选择性地探测 PKC 介导的激素、细胞因子和生长因子信号转导途径。它能抑制完整血小板和 T 细胞中的 PKC、Fas 介导的细胞凋亡、T 细胞介导的自身免疫性疾病以及 GSK-3。GSK-3 强效抑制剂(IC 50 = 360 nM)。强效 5-HT3 拮抗剂(K i = 29.5 nM)。 |
应用 | A highly selective inhibitor of all PKC isoforms and slight inhibitor of GSK-3 |
储存温度 | 2-8°C储存 |
运输条件 | 冰袋运输 |
作用类型 | 抑制剂 |
作用机制 | 蛋白激酶 C alpha 抑制剂;蛋白激酶 C beta 抑制剂;蛋白激酶 C gamma 抑制剂 |
备注 | 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
产品介绍 |
GF109203X是一种有效的PKC抑制剂,抑制PKCα, PKCβI, PKCβII和PKCγ,IC50分别为20 nM, 17 nM, 16nM和20 nM,作用于PKC比作用于EGFR, PDGFR和胰岛素受体选择性高3000倍以上。 A highly selective inhibitor of all PKC isoforms and slight inhibitor of GSK-3 GF109203X is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ, respectively, showing more than 3000-fold selectivity for PKC as compared to EGFR, PDGFR and insulin receptor. |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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分子类型 | 小分子 |
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IUPAC Name | 3-[1-[3-(dimethylamino)propyl]indol-3-yl]-4-(1H-indol-3-yl)pyrrole-2,5-dione |
INCHI | InChI=1S/C25H24N4O2/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) |
InChi Key | QMGUOJYZJKLOLH-UHFFFAOYSA-N |
Canonical SMILES | CN(C)CCCN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CNC5=CC=CC=C54 |
Isomeric SMILES | CN(C)CCCN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CNC5=CC=CC=C54 |
WGK Germany | 3 |
RTECS | UX9590000 |
PubChem CID | 2396 |
分子量 | 412.48 |
溶解性 | Soluble in DMSO (~1 mg/ml), DMF (10 mg/ml; warm to 40°C & vortex well), and 1:10 DMSO:PBS (pH 7.2) (~0.1 mg/ml). Insoluble in water. |
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敏感性 | 对热敏感 |
熔点 | 270 °C |
分子量 | 412.500 g/mol |
XLogP3 | 3.100 |
氢键供体数Hydrogen Bond Donor Count | 2 |
氢键受体数Hydrogen Bond Acceptor Count | 3 |
可旋转键计数Rotatable Bond Count | 6 |
精确质量Exact Mass | 412.19 Da |
单同位素质量Monoisotopic Mass | 412.19 Da |
拓扑极表面积Topological Polar Surface Area | 70.100 Ų |
重原子数Heavy Atom Count | 31 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 748.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 1 |
Purity(HPLC) | 98-100(%) |
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Appearance(G129390) | Orange to Dark Red Powder or Film |
Proton NMR spectrum | Conforms to Structure |
Solubility in CHCL3/MeOH (1/1),Orange to Red Clear to Hazy(1mg/0.7 ml) | pass |
1. Li M et al.. (2017) Protein Kinase C Mediates the Corticosterone-induced Sensitization of Dorsal Root Ganglion Neurons Innervating the Rat Stomach.. J Neurogastroenterol Motil, 23 (3): (464-476). [PMID:28343377] |
1. Toullec D, Pianetti P, Coste H, Bellevergue P, Grand-Perret T, Ajakane M, Baudet V, Boissin P, Boursier E, Loriolle F et al.. (1991) The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C.. J Biol Chem, 266 (24): (15771-81). [PMID:1874734] [10.1021/op500134e] |
2. Wu K et al.. (2021) Activity- and sleep-dependent regulation of tonic inhibition by Shisa7.. Cell Rep, 34 (12): (108899). [PMID:33761345] |
3. Sutherland-Deveen ME et al.. (2019) Differential Regulation of Human Ether-à-Go-Go-Related Gene (hERG) Current and Expression by Activation of Protein Kinase C.. Mol Pharmacol, 96 (1-12). [PMID:31015282] |
4. Du Y et al.. (2021) Kv1.5 channels are regulated by PKC-mediated endocytic degradation.. J Biol Chem, 296 (100514). [PMID:33676894] |
5. Li M et al.. (2017) Protein Kinase C Mediates the Corticosterone-induced Sensitization of Dorsal Root Ganglion Neurons Innervating the Rat Stomach.. J Neurogastroenterol Motil, 23 (3): (464-476). [PMID:28343377] |