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| | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole Basic information |
| Product Name: | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole | | Synonyms: | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole;1,3,4-Oxadiazole, 2,5-bis[3-(2-oxiranylmethoxy)phenyl]-;GAPDH inhibitor compound F8;GAPDH-IN-1 | | CAS: | 252212-58-1 | | MF: | C20H18N2O5 | | MW: | 366.37 | | EINECS: | | | Product Categories: | | | Mol File: | 252212-58-1.mol | ![2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole Structure](CAS/20180720/GIF/252212-58-1.gif) |
| | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole Chemical Properties |
| Boiling point | 584.4±58.0 °C(Predicted) | | density | 1.318±0.06 g/cm3(Predicted) | | solubility | Acetonitrile: Slightly soluble: 0.1-1 mg/ml | | pka | -5.20±0.45(Predicted) |
| | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole Usage And Synthesis |
| Uses | GAPDH-IN-1 (Compound F8) is a GAPDH inhibitor (IC50 of 39.31 μM for GAPDH enzymatic activity). GAPDH-IN-1 forms a covalent adduct with an aspartic acid in the active site to displace NAD+, a cofactor of the enzyme, with concomitant enhancement of the cysteine-reactive probe reaction with the catalytic cysteine[1]. | | References | [1] Jung Y, et al. Discovery of Non-Cysteine-Targeting Covalent Inhibitors by Activity-Based Proteomic Screening with a Cysteine-Reactive Probe. ACS Chem Biol. 2022 Feb 18;17(2):340-347. DOI:10.1021/acschembio.1c00824 |
| | 2,5-bis[3-(oxiran-2-ylmethoxy)phenyl]-1,3,4-oxadiazole Preparation Products And Raw materials |
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