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Chemical Formula | C14H20N2O16P2 |
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Molecular Weight | 534.26 Daltons | |
Monoisotopic Mass | 536.0444556901999 Daltons |
SMILES | C3(OC(OP(OP(OC[C@@H]2([C@H]([C@H]([C@H](N1(\C=C/C(=O)NC1=O))O2)O)O))(=O)[O-])(=O)[O-])[C@H](O)[C@@H](O)[C@H](O)3) |
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InChI | InChI=1S/C14H22N2O16P2/c17-5-3-28-13(11(22)8(5)19)31-34(26,27)32-33(24,25)29-4-6-9(20)10(21)12(30-6)16-2-1-7(18)15-14(16)23/h1-2,5-6,8-13,17,19-22H,3-4H2,(H,24,25)(H,26,27)(H,15,18,23)/p-2/t5-,6-,8+,9-,10-,11-,12-,13?/m1/s1 |
InChIKey | InChIKey=DQQDLYVHOTZLOR-WZNRFRBMSA-L |
Description: UDP-D-Xyl (Uridine Diphosphate-D-Xylose) is a nucleotide sugar composed of uridine diphosphate (UDP) linked to D-xylose, a pentose sugar. This molecule plays a vital role in the biosynthesis of glycosaminoglycans, polysaccharides, and other glycoconjugates, particularly in plants, animals, and microorganisms.
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Conclusion: UDP-D-Xyl is an essential nucleotide sugar involved in the biosynthesis of glycosaminoglycans in animals and hemicelluloses in plants. Its role in cell wall integrity, tissue repair, and various biological processes makes it a significant molecule for research in both health and agricultural sciences. The potential to manipulate UDP-D-Xyl pathways offers opportunities for therapeutic advancements and innovations in biotechnology and bioengineering
Size | 15 MG, 25 MG, 5 MG |
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10 in stock
10 in stock
IUPAC:Fuc(a1-2)[GalNAc(a1-3)]Gal(b1-3)GlcNAc(b1-3)Gal(b1-4)b-Glc, G82858KU
10 in stock
10 in stock
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