受注:045-509-1970 |
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Synonyms | IDH-C35 | Storage (From the date of receipt) |
3 years -20°C powder 1 years -80°C in solvent |
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化学式 | C27H31FN4O2 |
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分子量 | 462.56 | CAS No. | 1355326-35-0 | ||||
Solubility (25°C)* | 体外 | DMSO | 46 mg/mL (99.44 mM) | ||||
Ethanol | 30 mg/mL (64.85 mM) | ||||||
Water | Insoluble | ||||||
体内 (毎回新しく調製した物を用意してください) |
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* <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. |
製品説明 | AGI-5198 (IDH-C35) is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM. |
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in vitro | AGI-5198, potently inhibits mutant IDH1 (R132H-IDH1 and R132C-IDH1), but not wildtype IDH1 (IC50 > 100 μM) or any of IDH2 isoforms (R140Q, R172K, wildtype) (IC50 > 100 μM). AGI-5198, has been shown to have anti-tumor efficacy in the TS603 glioma cell line and to block R-2HG production in a dose-dependent manner. Under conditions of near-complete R-2HG inhibition, AGI-5198 induced demethylation of histone H3K9me3 and expression of genes associated with gliogenic differentiation. Blockade of mIDH1 impaired the growth of IDH1-mutant—but not IDH1–wild-type—glioma cells without appreciable changes in genome-wide DNA methylation. [1] |
in vivo | In R132H-IDH1 glioma xenografts, AGI-5198 (450 mg/kg/day) causes 50-60% growth inhibition over a treatment period of three weeks with no affect in the growth of IDH1 wild-type glioma xenografts. Tumors from AGI-5198-treated mice shows reduced staining with an antibody against the Ki-67 protein. But cleaved caspase-3 shows no differences between tumors from vehicle and AGI-5198–treated mice. [1] |
キナーゼアッセイ | IDH enzyme activity | |
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Compound is prepared as 10 mM stock in DMSO and diluted to 50X final concentration in DMSO, for a 50 μL reaction mixture. IDH enzyme activity converting alpha-ketogluta rate to 2-hydroxyglutarate is measured using a NADPH depletion assay. In the assay the remaining cofactor is measured at the end of the reaction with the addition of a catalytic excess of diaphorase and resazurin, to generate a fluorescent signal in proportion to the amount of NADPH remaining. IDH enzyme activity in the direction of isocitrate to alpha-ketoglutarate conversion is measured by direct coupling of the NADPH production to conversion of resazurin to resorufin by diaphorase. In both cases, resorufin is measured fluorometrically at Ex544 Em 590. | ||
細胞アッセイ | 細胞株 | TS603 |
濃度 | 0, 23.4, 93.8, 375, 3000 nM | |
反応時間 | -- | |
実験の流れ | soft-agar colony formation |
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動物実験 | 動物モデル | IDH1 mutant glioma xenografts |
投薬量 | 150 mg/kg, 450 mg/kg per day | |
投与方法 | gavage |
Data from [Data independently produced by , , J BIOL CHEM, 2018, doi:10.1074/jbc.RA117.001385]
High-Content and High-Throughput Clonogenic Survival Assay Using Fluorescence Barcoding [ Cancers -Basel), 2023, 15(19)4772] | PubMed: 37835466 |
Integrative analysis of drug response and clinical outcome in acute myeloid leukemia [ Cancer Cell, 2022, S1535-6108(22)00312-9] | PubMed: 35868306 |
Loss of FBXW7 Correlates with Increased IDH1 Expression in Glioma and Enhances IDH1-Mutant Cancer Cell Sensitivity to Radiation [ Cancer Res, 2022, 82(3):497-509] | PubMed: 34737211 |
Poly(ADP-ribose) glycohydrolase inhibition sequesters NAD+ to potentiate the metabolic lethality of alkylating chemotherapy in IDH mutant tumor cells [ Cancer Discov, 2020, CD-20-0226] | PubMed: 32606138 |
Poly(ADP-ribose) Glycohydrolase Inhibition Sequesters NAD+ to Potentiate the Metabolic Lethality of Alkylating Chemotherapy in IDH-Mutant Tumor Cells [ Cancer Discov, 2020, 10(11):1672-1689] | PubMed: 32606138 |
Triptolide Suppresses IDH1-mutated Malignancy via Nrf2-driven Glutathione Metabolism [ Proc Natl Acad Sci U S A, 2020, 5;117(18):9964-9972] | PubMed: 32312817 |
IDH1-R132H mutation radiosensitizes U87MG glioma cells via epigenetic downregulation of TIGAR. [ Oncol Lett, 2020, 19(2):1322-1330] | PubMed: 31966064 |
RNA-Binding Protein HuR Regulates Both Mutant and Wild-Type IDH1 in IDH1-Mutated Cancer [ Mol Cancer Res, 2019, 17(2):508-520] | PubMed: 30266754 |
Heterozygous IDH1R132H/WT created by "single base editing" inhibits human astroglial cell growth by downregulating YAP [ Oncogene, 2018, 37(38):5160-5174] | PubMed: 29849122 |
IDH1 Arg-132 mutant promotes tumor formation through down-regulating p53 [ J Biol Chem, 2018, 293(25):9747-9758] | PubMed: 29743236 |
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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