V = 1078.3(5) x lo6 pm3, psalsd = 1.089 g ~m -~, Z = 2, crystal size 0.3 x 0.3 x 0.9 mm3, 173 K, Cu,,, radiation, Enraf-Nonius CAD4, scan width 2.25 <8 < 76.5",4202 symmetry-independent and significant reflections [IF1 >3u(F)] structure solution by direct methods (SHELXS-86 [6]) supplemented by diff
Enzymatic synthesis of [1-14C-N-acetyl, P18O2] cytidine monophosphate neuraminic acid
β Scribed by Erin E. Burke; Nicole A. Horenstein
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- French
- Weight
- 152 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.889
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β¦ Synopsis
A method for the enzymatic synthesis of [1-14 C-N-acetyl, P 18 O 2 ] cytidine monophosphate neuraminic acid (CMP-NeuAc) is described. Central to the synthesis of [1-14 C-N-acetyl, P 18 O 2 ]CMP-NeuAc was the enzymatic preparation of [g-P 18 O 3 ]ATP for use in a reaction with uridine kinase and cytidine to provide 5 0 -[P 18 O 3 ]CMP. The [1-14 C-N-acetyl, P 18 O 2 ]CMP-NeuAc isotopomer was then synthesized from a reaction involving nucleoside monophosphate kinase, pyruvate kinase and CMP-NeuAc synthetase. The isolated reaction yield was 35%.
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