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| MAK-683 Basic information |
Product Name: | MAK-683 | Synonyms: | CPD 1111;MAK-683;EED inhibitor-1;MAK 683;MAK-683;MAK683;N-[(5-Fluoro-2,3-dihydro-4-benzofuranyl)methyl]-8-(2-methyl-3-pyridinyl)-1,2,4-triazolo[4,3-c]pyrimidin-5-amine;N-[(5-FLUORO-2,3-DIHYDROBENZOFURAN-4-YL)METHYL]-8-(2-METHYL-3-PYRIDYL)-[1,2,4]TRIAZOLO[4,3-C]PYRIMID;1,2,4-Triazolo[4,3-c]pyrimidin-5-amine, N-[(5-fluoro-2,3-dihydro-4-benzofuranyl)methyl]-8-(2-methyl-3-pyridinyl)-;inhibit,MAK683,MAK-683,Inhibitor,Histone Methyltransferase,MAK 683 | CAS: | 1951408-58-4 | MF: | C20H17FN6O | MW: | 376.39 | EINECS: | | Product Categories: | | Mol File: | 1951408-58-4.mol | |
| MAK-683 Chemical Properties |
density | 1.47±0.1 g/cm3(Predicted) | storage temp. | Store at -20°C | solubility | DMSO: 15 mg/ml | form | A solid | pka | 2.70±0.12(Predicted) |
| MAK-683 Usage And Synthesis |
Description | MAK-683 is an inhibitor of trimethylation of histone 3 lysine 27 (H3K27) by polycomb repressive complex 2 (PRC2), a complex that includes embryonic ectoderm development protein (EED). MAK-683 has an IC50 value of 5.9 nM in an EED-H3K27me3 peptide competition binding assay and inhibits H3K27 trimethylation in G401 cells (IC50 = 2.6 nM). It inhibits proliferation of KARPAS422 B cell lymphoma cells with an IC50 value of 3 nM. | Uses | MAK-683 is a useful intermediate for the preparation of triazolopyrimidine compounds useful in the treatment of diseases or disorders mediated by EED and/or PRC2. EED inhibitor-1. |
| MAK-683 Preparation Products And Raw materials |
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