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| | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid Basic information |
| Product Name: | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid | | Synonyms: | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid;6-HYDROXY-2-(METHYLTHIO)-4-PYRIMIDINECARBOXYLIC ACID;6-Hydroxy-2-(methylthio)pyrimidine-4-carboxylic acid;2-(methylsulfanyl)-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid;2-(methylthio)-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid;2-(Methylthio)-6-oxo-3,6-dihydropyrimidine-4-carboxylic acid;4-Pyrimidinecarboxylic acid, 1,6-dihydro-2-(methylthio)-6-oxo-;6-Hydroxy-2-(Methylsulfanyl)-4-Pyrimidinecarboxylic | | CAS: | 6314-14-3 | | MF: | C6H6N2O3S | | MW: | 186.19 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 6314-14-3.mol |  |
| | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid Chemical Properties |
| storage temp. | 2-8°C, stored under nitrogen | | Appearance | Off-white to light yellow Solid |
| | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid Usage And Synthesis |
| Uses | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic Acid has shown binding to HCR-13pf of MMP-13 hemopexin domain with no crossreactivity to MMP-1 and 8 which could serve as building block for development of drug for osteoarthritis (OA) and rheumatoid arthritis (RA). It can be useful in the structure-activity relationship studies of pyrimidine base analogs as ligands of orotate phosphoribosyltransferase as well as allosteric inhibitors of a mammalian lectin. |
| | 6-Hydroxy-2-(methylsulfanyl)-4-pyrimidinecarboxylic acid Preparation Products And Raw materials |
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