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| | [5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-3-[2-[2-(2-hydroxy-3,7,11,15-tetramethyl-hexadecanoyl)sulfanylethylcarbamoyl]ethylcarbamoyl]-2,2-dimethyl-propoxy]-phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid Basic information |
| | [5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-3-[2-[2-(2-hydroxy-3,7,11,15-tetramethyl-hexadecanoyl)sulfanylethylcarbamoyl]ethylcarbamoyl]-2,2-dimethyl-propoxy]-phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid Chemical Properties |
| | [5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-3-[2-[2-(2-hydroxy-3,7,11,15-tetramethyl-hexadecanoyl)sulfanylethylcarbamoyl]ethylcarbamoyl]-2,2-dimethyl-propoxy]-phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid Usage And Synthesis |
| Uses | 2-Hydroxyphytanoyl-CoA is synthesised from 2-hydroxyphytanic acid using the acid anhydride method[1]. | | References | [1] N M Verhoeven, et al. Resolution of the Phytanic Acid a-Oxidation Pathway: Identification of Pristanal as Product of the Decarboxylation of 2-Hydroxyphytanoyl-CoA. Biochem Biophys Res Commun. 1997 Aug 8;237(1):33-6. DOI:10.1006/bbrc.1997.7066 |
| | [5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-3-[2-[2-(2-hydroxy-3,7,11,15-tetramethyl-hexadecanoyl)sulfanylethylcarbamoyl]ethylcarbamoyl]-2,2-dimethyl-propoxy]-phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid Preparation Products And Raw materials |
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