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Product Name: | IKE | Synonyms: | IKE);Imidazole ketone erastin
(Ferroptosis inducer IKE;Ferroptosis inducer IKE;IMIDAZOLE KETONE ERASTIN;FERROPTOSIS INDUCER IKE;IKE;Imidazole ketone erastin;4(3H)-Quinazolinone, 2-[[4-[2-(4-chlorophenoxy)acetyl]-1-piperazinyl]methyl]-3-[5-[2-(1H-imidazol-1-yl)acetyl]-2-(1-methylethoxy)phenyl]-;3-(5-(2-(1H-Imidazol-1-yl)acetyl)-2-isopropoxyphenyl)-2-((4-(2-(4-chlorophenoxy)acetyl)piperazin-1-yl)methyl)quinazolin-4(3H)-one;PUN-30119 | CAS: | 1801530-11-9 | MF: | C35H35ClN6O5 | MW: | 655.14 | EINECS: | | Product Categories: | | Mol File: | 1801530-11-9.mol | |
Boiling point | 886.5±75.0 °C(Predicted) | density | 1.34±0.1 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | DMF: 10mg/mL,DMSO: 1mg/mL,DMSO:PBS (pH 7.2) (1:2): 0.25mg/mL | form | A crystalline solid | pka | 6.12±0.10(Predicted) |
Description | Imidazole ketone erastin is an inducer of ferroptosis. It inhibits glutamate release in human CCF-STTG1 astrocytoma cells (IC50 = 30 nM), indicating inhibition of the system xc- cystine/glutamate transporter. Imidazole ketone erastin increases production of lipid reactive oxygen species (ROS) in SUDHL6 diffuse large B cell lymphoma (DLBCL) cells in a concentration-dependent manner, as well as reduces glutathione (GSH) levels in these cells (IC50 = 34 nM). It inhibits the growth of HT-1080 fibrosarcoma cells (GI50 = 310 nM) as well as HRASG12V-overexpressing BJeLR cells (IC50 = 3 nM). Imidazole ketone erastin (23 and 40 mg/kg) reduces tumor growth in an SUDHL6 mouse xenograft model. | Uses | PUN30119 is potent, metabolically stable inhibitor of system xc. |
| IKE Preparation Products And Raw materials |
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