IKE (Imidazole Ketone Erastin)

製品コードS8877 バッチS887702

印刷

化学情報

 Chemical Structure Synonyms PUN30119 Storage
(From the date of receipt)
3 years -20°C powder
化学式

C35H35ClN6O5

分子量 655.14 CAS No. 1801530-11-9
Solubility (25°C)* 体外 DMSO 100 mg/mL (152.63 mM)
Ethanol 100 mg/mL (152.63 mM)
Water 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 IKE(Imidazole ketone erastin) is a potent, selective, and metabolically stable system xc– inhibitor and inducer of ferroptosis.
in vitro

Imidazole ketone erastin (IKE) is an erastin analog with nanomolar potency, high metabolic stability, and intermediate water solubility. Its treatment potently reduces DLBCL cell number[1].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 DLBCL cell line
濃度 0-100 μM
反応時間 24 h
実験の流れ

DLBCL cells are plated at 10,000 cells per well in white 384-well plates (32 μL per well) in technical duplicates and incubated overnight. The cells are then treated with 8 μL medium containing a two-fold dilution series of vehicle (DMSO), IKE (starting from 100 μM) with or without Fer-1 (starting from 200 μM). After 24 h incubation, 40 μL of 50% CellTiter-Glo / 50% cell culture medium is added to each well and incubated at room temperature with shaking for 15 min. Luminescence is measured. All cell viability data are normalized to the DMSO vehicle condition. Experiments are performed three independent times with different passages for each cell line. From these data, dose-response curves and IC50 values are computed.

動物実験 動物モデル Non-obese diabetic/ severe combined immunodeficiency (NOD/SCID) mice
投薬量 50 mg/kg
投与方法 IP, IV and oral administration

参考

  • https://pubmed.ncbi.nlm.nih.gov/30799221/

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:

SLC7A11 is an unconventional H+ transporter in lysosomes [ Cell, 2025, S0092-8674(25)00406-4] PubMed: 40280132
Endoplasmic reticulum-mitochondria contacts are prime hotspots of phospholipid peroxidation driving ferroptosis [ Nat Cell Biol, 2025, 27(6):902-917] PubMed: 40514428
BDH2-driven lysosome-to-mitochondria iron transfer shapes ferroptosis vulnerability of the melanoma cell states [ Nat Metab, 2025, 7(9):1851-1870] PubMed: 40957995
Targeting pancreatic cancer glutamine dependency confers vulnerability to GPX4-dependent ferroptosis [ Cell Rep Med, 2025, 6(2):101928] PubMed: 39879992
Vorapaxar enhanced mitochondria-associated ferroptosis primes cancer immunotherapy via targeting FOXO1/HMOX1 axis [ Cell Rep Med, 2025, 6(10):102371] PubMed: 41005298
Neutralization of acyl coenzyme A binding protein for the experimental prevention and treatment of hepatocellular carcinoma [ Cell Rep Med, 2025, 6(7):102232] PubMed: 40628264
SLC25A1 and ACLY maintain cytosolic acetyl-CoA and regulate ferroptosis susceptibility via FSP1 acetylation [ EMBO J, 2025, 10.1038/s44318-025-00369-5] PubMed: 39881208
Periplocin potentiates ferroptotic cell death in non-small cell lung cancer by inducing the degradation of Nrf2 [ Cancer Cell Int, 2025, 25(1):294] PubMed: 40760694
Mitochondrial phosphoenolpyruvate carboxykinase 2 counteracts ferroptosis via catalytic activity independent of mitochondrial stress [ Biochem Biophys Res Commun, 2025, 778:152383] PubMed: 40712389
Targeting lipid scrambling potentiates ferroptosis and triggers tumor immune rejection [ Sci Adv, 2025, 11(33):eadx6587] PubMed: 40815641

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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