A4847
阿特波龙
≥98% (HPLC), GSK-3β and CDK5/p25 inhibitor, powder
别名:
9-硝基-7,12-二氢吲哚o[3,2-d][1]苯并氮杂卓-6(5H)-酮
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关于此项目
经验公式（希尔记法）:
C16H11N3O3
化学文摘社编号:
分子量:
293.28
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
阿特波龙, ≥98% (HPLC), powder
Quality Level
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
yellow to brown
solubility
DMSO: ≥10 mg/mL
storage temp.
2-8°C
SMILES string
[O-][N+](=O)c1ccc2[nH]c-3c(CC(=O)Nc4ccccc-34)c2c1
InChI
1S/C16H11N3O3/c20-15-8-12-11-7-9(19(21)22)5-6-14(11)18-16(12)10-3-1-2-4-13(10)17-15/h1-7,18H,8H2,(H,17,20)
InChI key
OLUKILHGKRVDCT-UHFFFAOYSA-N
Gene Information
rat ... Gsk3b(84027)
Application
Alsterpaullone 已用于稳定 β-catenin。
Alsterpaullone 抑制 GSK-3β、CDK5/p25 和 CDK1/cyclinB。Alsterpaullone 也已被作为抗躁狂药进行研究，用于双相情感障碍急性躁狂期的治疗。
Biochem/physiol Actions
Alsterpaullone（ALP）是一种细胞周期蛋白依赖性激酶（CDK）抑制剂。它被认为是第 3 组髓母细胞瘤的治疗药物。Alsterpaullone 调节细胞周期的进程。它可以通过干扰线粒体膜电位来激活 caspase-9，从而阻止细胞周期并刺激癌细胞凋亡。
GSK-3β 和 CDK5/p25; 的有效和选择性抑制剂；CDK1/cyclin B 的有效抑制剂（IC50 = 0.035 μM）。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Laura Iglesias Ollé et al.
Biomedicines, 12(6) (2024-06-27)
Hydra head formation depends on an organizing center in which Wnt/β-catenin signaling, that plays an inductive role, positively regulates Sp5 and Zic4, with Sp5 limiting Wnt3/β-catenin expression and Zic4 triggering tentacle formation. Using transgenic lines in which the HySp5 promoter
Mikhail Kalinichev et al.
The international journal of neuropsychopharmacology, 14(8), 1051-1067 (2011-01-07)
There is a growing body of evidence suggesting that animal models can be developed to probe the specific domains of bipolar disorder (BD) using the endophenotype approach. Here we tested clinically active antimanic drugs to validate amphetamine-induced hyperactivity in Black
C Schultz et al.
Journal of medicinal chemistry, 42(15), 2909-2919 (1999-07-30)
The paullones represent a novel class of small molecule cyclin-dependent kinase (CDK) inhibitors. To investigate structure-activity relationships and to develop paullones with antitumor activity, derivatives of the lead structure kenpaullone (9-bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6(5H)-one, 4a) were synthesized. Paullones with different substituents in the
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A4847-1MG | 04061826128671 |