AZD1208

製品コードS7104 バッチS710403

印刷

化学情報

Chemical Structure Synonyms N/A Storage
(From the date of receipt)		 3 years -20°C powder
1 years -80°C in solvent
化学式

C21H21N3O2S
分子量 379.48 CAS No. 1204144-28-4
Solubility (25°C)* 体外 DMSO (warmed with 50ºC water bath) 75 mg/mL (197.63 mM)
Water Insoluble
Ethanol Insoluble
体内 （毎回新しく調製した物を用意してください）
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明 AZD1208 is a potent, and orally available Pim kinase inhibitor with IC50 of 0.4 nM, 5 nM, and 1.9 nM for Pim1, Pim2, and Pim3 in cell-free assays, respectively. AZD1208 induces autophagy, cell cycle arrest and apoptosis. Phase 1.
in vitro

AZD1208 is an orally available, potent and highly selective Pim inhibitor that effectively inhibits all three isoforms. This compound inhibits the growth of several AML cell lines and sensitivity correlates with the level of Pim-1 expression, STAT5 activation and presence of protein tyrosine kinase mutation. It causes cell cycle arrest and apoptosis in MOLM-16 cells in culture. This is accompanied by a dose-dependent reduction in phosphorylation of BAD, 4EBP1 and p70S6K. In addition, this chemical leads to potent inhibition of colony growth of primary AML cells from bone marrow aspirates and downregulates phosphorylation of Pim targets. [1]
in vivo

AZD1208 suppresses the growth of MOLM-16 and KG-1a xenograft tumors in vivo in a dose proportional manner. [1]
特徴 Orally bioavailable Pim kinase inhibitor that has been tested in Phase I clinical trials for treatment of advanced solid tumors and malignant lymphoma.

プロトコル(参考用のみ)

細胞アッセイ 細胞株 MDSCs
濃度 1 μM
反応時間 4 h
実験の流れ Bone marrow derived MDSCs were separated into M-MDCSs and suppressive neutrophils by FACS, then plated in RPMI with 10% FBS in the presence of DMSO or AZD1208 for 4 hours on coverslips.
動物実験 動物モデル Female CB17 SCID mice
投薬量 10 & 30 mg/kg
投与方法 o.g.

参考

  • https://ash.confex.com/ash/2011/webprogram/Paper41793.html
  • https://pubmed.ncbi.nlm.nih.gov/34038722/
  • https://pubmed.ncbi.nlm.nih.gov/24363397/

カスタマーフィードバック

, , Blood, 2016, 127(20):2439-50.

Data from [Data independently produced by , , Leukemia, 2018, 32(3):597-605]

Data from [Data independently produced by , , Mol Cancer Ther, 2018, 17(4):849-857]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

PIM2 inhibition promotes MCL1 dependency in plasma cells involving integrated stress response-driven NOXA expression [ Nat Commun, 2025, 16(1):256] PubMed: 39747141
2-Desaza-annomontine (C81) impedes angiogenesis through reduced VEGFR2 expression derived from inhibition of CDC2-like kinases [ Angiogenesis, 2024, 10.1007/s10456-024-09906-y] PubMed: 38403816
ELK3 destabilization by speckle-type POZ protein suppresses prostate cancer progression and docetaxel resistance [ Cell Death Dis, 2024, 15(4):274] PubMed: 38632244
The role of Pim-1 kinases in inflammatory signaling pathways [ Inflamm Res, 2024, 10.1007/s00011-024-01924-2] PubMed: 39079978
CDK9 inhibition induces epigenetic reprogramming revealing strategies to circumvent resistance in lymphoma [ Mol Cancer, 2023, 22(1):64] PubMed: 36998071
A novel IRAK4/PIM1 inhibitor ameliorates rheumatoid arthritis and lymphoid malignancy by blocking the TLR/MYD88-mediated NF-κB pathway [ Acta Pharm Sin B, 2023, 13(3):1093-1109] PubMed: 36970199
Nuclear transport surveillance of p53 by nuclear pores in glioblastoma [ Cell Rep, 2023, S2211-1247(23)00893-8] PubMed: 37552992
Targeting macrophagic PIM-1 alleviates osteoarthritis by inhibiting NLRP3 inflammasome activation via suppressing mitochondrial ROS/Cl- efflux signaling pathway [ J Transl Med, 2023, 21(1):452] PubMed: 37422640
Simultaneous Inhibition of ErbB3 and Calmodulin-Mediated Signaling Effectively Inhibits Malignant Peripheral Nerve Sheath Tumor Proliferation and Survival [ Medical University of South Carolina, 2023, ] PubMed: None
Pivotal role of PIM2 kinase in plasmablast generation and plasma cell survival, opening new treatment options in myeloma [ Blood, 2022, blood.2021014011] PubMed: 35108359

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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