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Chemical Structure| 27821-45-0 Chemical Structure| 27821-45-0

Structure of 27821-45-0

Chemical Structure| 27821-45-0

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UDP disodium salt is an endogenous agonist of P2Y receptor which preferentially activates P2Y6. It exhibis antagonistic effect on the P2Y14 receptor.

Synonyms: UDP disodium salt

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Product Citations

Product Citations

Moore, Maxwell J. ; Qin, Pengjin ; Keith, D. Jamin ; Boger, Dale L. ;

Abstract: Modifications to the enzymic glycosylation of vancomycin and its residue 4 thioamide analog are detailed that significantly reduce the enzyme loading and amount of glycosyl donor needed for each glycosylation reaction, provide a streamlined synthesis and replacement for the synthetic UDP-vancosamine glycosyl donor to improve both access and storage stability, and permit a single-pot, two-step conversion of the aglycons to the fully glycosylated synthetic glycopeptides now conducted at higher concentrations The improvements are exemplified with the two-step, one-pot glycosylation of [Ψ[C(=S)NH]Tpg4]vancomycin aglycon (92%) conducted on a 400 mg scale (2 mg-1 g scales) and vancomycin aglycon itself (5 mg scale, 84%).

Keywords: Vancomycin ; Vancomycin analogues ; Enzymatic glycosylation

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Product Details of Uridine-5'-diphosphate disodium salt

CAS No. :27821-45-0
Formula : C9H12N2Na2O12P2
M.W : 448.12
SMILES Code : O[C@@H]([C@H]([C@H](N1C(NC(C=C1)=O)=O)O2)O)[C@H]2COP([O-])(OP([O-])(O)=O)=O.[Na+].[Na+]
Synonyms :
UDP disodium salt
MDL No. :MFCD00084679

Safety of Uridine-5'-diphosphate disodium salt

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Uridine-5'-diphosphate disodium salt

GPCR

Isoform Comparison

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.23mL

0.45mL

0.22mL

11.16mL

2.23mL

1.12mL

22.32mL

4.46mL

2.23mL

 

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