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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| A134722-2mg |
2mg |
现货 ![]() |
| |
| A134722-5mg |
5mg |
现货 ![]() |
| |
| A134722-10mg |
10mg |
现货 ![]() |
| |
| A134722-25mg |
25mg |
现货 ![]() |
| |
| A134722-50mg |
50mg |
现货 ![]() |
| |
| A134722-100mg |
100mg |
现货 ![]() |
|
| 别名 | 9-溴-7,12-二氢-吡啶并[3',2':2,3]吖庚因并[4,5-b]吲哚-6(5H)-酮 |
|---|---|
| 英文别名 | 9-Bromo-7,12-dihydro-pyrido[3′,2′:2,3]azepino[4,5-b]indol-6(5H)-one | 1-Akp |
| 规格或纯度 | Moligand™, ≥97%(HPLC) |
| 英文名称 | 1-Azakenpaullone |
| 生化机理 | 1-Azakenpaullone 是一种细胞渗透性、有效的选择性糖原合酶激酶 3 抑制剂3β (GSK3β)与 CDK 的交叉反应性低 100 倍。1-Azakenpaullone 可与 BIO 和 CHIR99021 一起用作 GSK3 抑制的“金标准”。 1-氮杂坎帕罗酮(AZP)可刺激β-连环蛋白相关基因的转录。该化合物能诱导β细胞的增殖和复制。 |
| 储存温度 | 避光,-20°C储存 |
| 运输条件 | 超低温冰袋运输 |
| 作用类型 | 抑制剂 |
| 作用机制 | 细胞周期蛋白依赖性激酶 1 抑制剂;细胞周期蛋白依赖性激酶 5 抑制剂;糖原合酶激酶 3 beta 抑制剂 |
| 产品介绍 |
1-Azakenpaullone (1-Akp)是一种高度选择性GSK-3β抑制剂,IC50为18 nM, 其选择性高于CDK1/cyclin B 和 CDK5/p25 100倍。 |
| 纯度 | ≥97%(HPLC) |
| 活性类型 | Relation | Activity value | Units | Action Type | 期刊 | PubMed Id | doi | Assay Aladdin ID |
|---|
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
| 分子类型 | 小分子 |
|---|---|
| IIUPAC Name | 14-bromo-3,8,18-triazatetracyclo[9.7.0.02,7.012,17]octadeca-1(11),2(7),3,5,12(17),13,15-heptaen-9-one |
| INCHI | 1S/C15H10BrN3O/c16-8-3-4-11-9(6-8)10-7-13(20)18-12-2-1-5-17-15(12)14(10)19-11/h1-6,19H,7H2,(H,18,20) |
| InChi Key | NTSBZVCEIVPKBJ-UHFFFAOYSA-N |
| Smiles | C1C2=C(C3=C(C=CC=N3)NC1=O)NC4=C2C=C(C=C4)Br |
| Isomeric SMILES | C1C2=C(C3=C(C=CC=N3)NC1=O)NC4=C2C=C(C=C4)Br |
| 分子量 | 328.16 |
| Reaxy-Rn | 9571784 |
| Reaxys-RN link address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9571784&ln= |
| 溶解性 | DMSO: >10 mg/mL |
|---|---|
| 敏感性 | 对空气敏感;对光线敏感 |
| 分子量 | 328.160 g/mol |
| XLogP3 | 2.200 |
| 氢键供体数Hydrogen Bond Donor Count | 2 |
| 氢键受体数Hydrogen Bond Acceptor Count | 2 |
| 可旋转键计数Rotatable Bond Count | 0 |
| 精确质量Exact Mass | 327.001 Da |
| 单同位素质量Monoisotopic Mass | 327.001 Da |
| 拓扑极表面积Topological Polar Surface Area | 57.800 Ų |
| 重原子数Heavy Atom Count | 20 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 405.000 |
| 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 |
| WGK Germany | 2 |
|---|
| 1. Eldar-Finkelman H, Schreyer SA, Shinohara MM, LeBoeuf RC, Krebs EG. (1999) Increased glycogen synthase kinase-3 activity in diabetes- and obesity-prone C57BL/6J mice.. Diabetes, 48 (8): (1662-6). [PMID:10426388] |
| 2. Nikoulina SE, Ciaraldi TP, Mudaliar S, Mohideen P, Carter L, Henry RR. (2000) Potential role of glycogen synthase kinase-3 in skeletal muscle insulin resistance of type 2 diabetes.. Diabetes, 49 (2): (263-71). [PMID:10868943] |
| 3. Kunick C, Lauenroth K, Leost M, Meijer L, Lemcke T. (2004) 1-Azakenpaullone is a selective inhibitor of glycogen synthase kinase-3 beta.. Bioorg Med Chem Lett, 14 (2): (413-6). [PMID:14698171] |
| 4. Cai Z, Zhao Y, Zhao B. (2012) Roles of glycogen synthase kinase 3 in Alzheimer's disease.. Curr Alzheimer Res, 9 (7): (864-79). [PMID:22272620] |
| 5. Hurtado DE, Molina-Porcel L, Carroll JC, Macdonald C, Aboagye AK, Trojanowski JQ, Lee VM. (2012) Selectively silencing GSK-3 isoforms reduces plaques and tangles in mouse models of Alzheimer's disease.. J Neurosci, 32 (21): (7392-402). [PMID:22623685] |
| 6. Takashima A, Noguchi K, Sato K, Hoshino T, Imahori K. (1993) Tau protein kinase I is essential for amyloid beta-protein-induced neurotoxicity.. Proc Natl Acad Sci USA, 90 (16): (7789-93). [PMID:8356085] |