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Encyclopedia

Uridine-5'-diphosphate-mannose

Base Information Edit
  • Chemical Name:Uridine-5'-diphosphate-mannose
  • CAS No.:16375-64-7
  • Molecular Formula:C15H24N2O17P2
  • Molecular Weight:566.306
  • Hs Code.:
  • DSSTox Substance ID:DTXSID501317582
  • Nikkaji Number:J855.604K
  • Wikidata:Q27466878
  • Metabolomics Workbench ID:147008
  • ChEMBL ID:CHEMBL227711
  • Mol file:16375-64-7.mol
Uridine-5'-diphosphate-mannose

Synonyms:URIDINE-5'-DIPHOSPHATE-MANNOSE;CHEMBL227711;UDP-Mannose;D0Z9JO;SCHEMBL1520993;DTXSID501317582;BDBM50209666;DB02421;URIDINE-5''-DIPHOSPHATE-MANNOSE;UFM;Q27466878

Suppliers and Price of Uridine-5'-diphosphate-mannose
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 16 raw suppliers
Chemical Property of Uridine-5'-diphosphate-mannose Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:316.61000 
  • Density:2.026g/cm3 
  • LogP:-4.79370 
  • XLogP3:-6.3
  • Hydrogen Bond Donor Count:9
  • Hydrogen Bond Acceptor Count:17
  • Rotatable Bond Count:9
  • Exact Mass:566.05502130
  • Heavy Atom Count:36
  • Complexity:964
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)O)O)O)O)O
  • Isomeric SMILES:C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)O[C@@H]3[C@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O
Technology Process of Uridine-5'-diphosphate-mannose

There total 19 articles about Uridine-5'-diphosphate-mannose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With galactokinase; pyruvate kinase; inorganic pyrophosphatase; phosphoenolpyruvic acid; galactose-1-phosphate uridylyltransferase; GalU; ATP; uridine-5'-diphosphoglucose; at 30 ℃; for 24h; pH=8; aq. phosphate buffer; Inert atmosphere;
DOI:10.1039/b815549f
Guidance literature:
With recombinant Bifidobacterium infantis ATCC15697 N-acetylhexosamine 1-kinase; recombinant Bifidobacterium longum ATCC55813 UDP-sugar pyrophosphorylase; recombinant Pasteurella multocida P-1059 inorganic pyrophosphatase; ATP; magnesium chloride; at 37 ℃; for 24h; pH=8; aq. buffer; Enzymatic reaction;
DOI:10.1039/c2cc17577k
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