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| | Acetic acid, 2-[3-[[3'-[[[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]amino]carbonyl]-5'-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4'-methyl[1,1'-biphenyl]-4-yl]oxy]propoxy]- Basic information |
| | Acetic acid, 2-[3-[[3'-[[[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]amino]carbonyl]-5'-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4'-methyl[1,1'-biphenyl]-4-yl]oxy]propoxy]- Chemical Properties |
| Boiling point | 831.0±65.0 °C(Predicted) | | density | 1+-.0.06 g/cm3(Predicted) | | storage temp. | 4°C, away from moisture | | solubility | DMSO : ≥ 160 mg/mL (264.15 mM) | | form | Solid | | pka | 3.47±0.10(Predicted) | | color | Yellow to brown |
| | Acetic acid, 2-[3-[[3'-[[[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]amino]carbonyl]-5'-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4'-methyl[1,1'-biphenyl]-4-yl]oxy]propoxy]- Usage And Synthesis |
| Uses | Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b) incorporates a ligand for EZH2, and a PROTAC linker, which recruit E3 ligases. Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b) can be used for the research of lymphoma[1]. | | IC 50 | EZH2 | | References | [1] Tu Y, et al. Design, Synthesis, and Evaluation of VHL-Based EZH2 Degraders to Enhance Therapeutic Activity against Lymphoma. J Med Chem. 2021 Jul 22;64(14):10167-10184. DOI:10.1021/acs.jmedchem.1c00460 |
| | Acetic acid, 2-[3-[[3'-[[[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]amino]carbonyl]-5'-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4'-methyl[1,1'-biphenyl]-4-yl]oxy]propoxy]- Preparation Products And Raw materials |
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