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受注:045-509-1970 |
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Synonyms | NUCC-0200975 | Storage (From the date of receipt) |
3 years -20°C powder | |||||||
| 化学式 | C25H16Cl2F6N2O2 |
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| 分子量 | 561.30 | CAS No. | 2289691-01-4 | ||||||||
| Solubility (25°C)* | 体外 | DMSO | 100 mg/mL (178.15 mM) | ||||||||
| Ethanol | 60 mg/mL (106.89 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. |
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| 製品説明 | MYCi975 (NUCC-0200975) is a potent, selective and orally active inhibitor of MYC that disrupts MYC/MAX interaction, promotes MYC T58 phosphorylation and MYC degradation, and impairs MYC driven gene expression. MYCi975 exhibits potent anti-tumor activities. |
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| in vitro | MYCi975 localizes to the same region of the MYC protei. Treatment of cells with this compound enhances MYC degradation and phosphorylation on T58. It also directly increases GSK3b-mediated MYC pT58 in the in vitro kinase assay.[1] |
| in vivo | MYCi975 suppresses in vivo tumor growth in mice, increases tumor immune cell infiltration, upregulates PD-L1 on tumors, and sensitizes tumors to anti-PD1 immunotherapy with good tolerability.[1] |
| 細胞アッセイ | 細胞株 | MycCaP, PC3, LNCaP, PC12, MV411, SK-N-BE (2), 293T, P493-6 B cells, LLC1 cells, TGR-1, HO15.19 Rat-1 cells |
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| 濃度 | 3-25 μM, 8 μM, 6 μM | |
| 反応時間 | 24 h | |
| 実験の流れ | PC3 cells are treated with 6 μM 361 or 8 μM MYCi975 and P493-6 cells are treated with 0.1 mg/ml Tetracycline or 6 μM this compound for 24 hr in triplicates. Then cells are washed with PBS and RNA is extracted using RNAeasy Plus mini kit. | |
| 動物実験 | 動物モデル | 6-8 weeks old FVB mice, prostate PDX model (TM00298), NSG mice, C57BL/6, CB17/Icr-Prkdcscid/IcrIcoCrl mice, CD-1 |
| 投薬量 | 50 mg/kg, 100 mg/kg | |
| 投与方法 | IP |
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| Reprogramming neuroblastoma by diet-enhanced polyamine depletion [ Nature, 2025, 646(8085):707-715] | PubMed: 40993392 |
| MYC plus class IIa HDAC inhibition drives mitochondrial dysfunction in non-small cell lung cancer [ Cell Rep, 2025, 44(6):115722] | PubMed: 40392656 |
| CD38 contributes to tumor progression and tumor microenvironment reshaping in epithelial ovarian cancer [ Transl Oncol, 2025, 57:102414] | PubMed: 40381484 |
| Cell-based high-throughput screening using a target-NanoLuc fusion construct to identify molecular glue degraders of c-Myc oncoprotein [ RSC Chem Biol, 2025, 10.1039/d5cb00093a] | PubMed: 40978459 |
| Substrate Stiffness Modulates Fibroblast Extracellular Vesicle Secretion via Mechanotransduction Pathways [ bioRxiv, 2025, 2025.07.29.667440] | PubMed: 40766685 |
| Metabolic imaging distinguishes ovarian cancer subtypes and detects their early and variable responses to treatment [ Oncogene, 2024, 10.1038/s41388-024-03231-w] | PubMed: 39639170 |
| The oncogenic axis YAP/MYC/EZH2 impairs PTEN tumor suppression activity enhancing lung tumorigenicity [ Cell Death Discov, 2024, 10(1):452] | PubMed: 39455556 |
| A program of successive gene expression in mouse one-cell embryos [ Cell Rep, 2023, 42(2):112023] | PubMed: 36729835 |
| Patient-Derived Triple-Negative Breast Cancer Organoids Provide Robust Model Systems That Recapitulate Tumor Intrinsic Characteristics [ Cancer Res, 2022, 82(7):1174-1192] | PubMed: 35180770 |
| Loss of G0/G1 switch gene 2 (G0S2) promotes disease progression and drug resistance in chronic myeloid leukaemia (CML) by disrupting glycerophospholipid metabolism [ Clin Transl Med, 2022, 12(12):e1146] | PubMed: 36536477 |
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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