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| | Sirt2-PROTAC-1 Basic information |
| Product Name: | Sirt2-PROTAC-1 | | Synonyms: | Sirt2-PROTAC-1;PROTAC Sirt2 Degrader-1;N-{4-[4-({3-[(2-{2-[(4,6-dimethylpyrimidin-2-yl)sulfanyl]acetamido}-1,3-thiazol-5-yl)methyl]phenoxy}methyl)-1H-1,2,3-triazol-1-yl]butyl}-2-{[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]oxy}acetamide | | CAS: | 2098487-75-1 | | MF: | C40H40N10O8S2 | | MW: | 852.94 | | EINECS: | | | Product Categories: | PROTACs-Please select | | Mol File: | 2098487-75-1.mol |  |
| | Sirt2-PROTAC-1 Chemical Properties |
| density | 1.52±0.1 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMSO : ≥ 100 mg/mL (117.24 mM);Water : < 0.1 mg/mL (insoluble) | | form | Solid | | pka | 7.94±0.50(Predicted) | | color | White to off-white |
| | Sirt2-PROTAC-1 Usage And Synthesis |
| Uses | PROTAC Sirt2 Degrader-1 is a SirReal-based PROTAC, acts as a Sirt2 degrader, composed of a highly potent and isotype-selective Sirt2 inhibitor, a linker, and a bona fide Cereblon ligand for E3 ubiquitin ligase. PROTAC Sirt2 Degrader-1 shows an IC50 of 0.25 μM for Sirt2, with no effect on Sirt1/Sirt3 (IC50s>100 μM)[1]. | | IC 50 | SIRT2: 0.25 μM (IC50) | | References | [1] Schiedel M, et al. Chemically Induced Degradation of Sirtuin 2 (Sirt2) by a Proteolysis Targeting Chimera (PROTAC) Based on Sirtuin Rearranging Ligands (SirReals). J Med Chem. 2018 Jan 25;61(2):482-491. DOI:10.1021/acs.jmedchem.6b01872 |
| | Sirt2-PROTAC-1 Preparation Products And Raw materials |
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