Uri­dine 5′-diphosphoglucose dis­odi­um salt CAS 28053-08-9

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• Prop­er­ties
• Safe­ty Data
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Iden­ti­fi­ca­tion

CAS Number

28053-08-9

Name

Uri­dine 5′-diphosphoglucose dis­odi­um salt

Syn­onyms

(3,4-Dihydroxytetrahydro-2-furanyl)methyl 3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl dihy­dro­gen diphos­phate [ACD/IUPAC Name]
(3,4-Dihydroxytetrahydro-2-furanyl)methyl-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yldihydrogendiphosphat [Ger­man] [ACD/IUPAC Name]
248-801-6 [EINECS]
28053-08-9 [RN]
Dihy­drogén­odiphos­phate de (3,4-dihydroxytétrahydro-2-furanyl)méthyle et de 3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yle [French] [ACD/IUPAC Name]

SMILES

C1C(C(C(O1)COP(=O)(O)OP(=O)(O)OC2C(C(C(C(O2)CO)O)O)O)O)O

Std­InChI

InChI=1S/C11H22O15P2/c12-1-5-8(15)9(16)10(17)11(24-5)25-28(20,21)26-27(18,19)23-3-6-7(14)4(13)2-22-6/h4-17H,1-3H2,(H,18,19)(H,20,21)

Std­InChIKey

ZZA­H­NEVHQY­WAEU-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C15H22N2Na2O17P2

Mol­e­c­u­lar Weight

610.26

EINECS

248-801-6

MDL Number

MFCD20441966

Prop­er­ties

Appear­ance

White pow­der or off- white powder

Safe­ty Data

Sym­bol

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our Uri­dine 5′-diphosphoglucose dis­odi­um salt CAS 28053-08-9

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Solu­tion Clar­i­ty and Color

Clar­i­fy, colorless

Loss on Drying

≤10.0%

Shelf Life

2 years

Stor­age

Store at -20°C for long time, in con­tain­er tight­ly sealed ; Pro­tect from light.

Known Appli­ca­tion

Inter­me­di­ate in Car­bo­hy­drate Metab­o­lism
UDP-Glc (Uri­dine Diphos­phate Glu­cose) is an essen­tial inter­me­di­ate in car­bo­hy­drate metab­o­lism, play­ing a cru­cial role par­tic­u­lar­ly in glyco­gen and gly­co­pro­tein syn­the­sis. As an acti­vat­ed form of glu­cose, it par­tic­i­pates in gly­co­syl trans­fer reac­tions by trans­fer­ring glu­cose units to oth­er molecules.

Donor in Gly­co­sy­la­tion Reac­tions
UDP-Glc serves as the pri­ma­ry donor in gly­co­syl­trans­ferase reac­tions and is fre­quent­ly used in the syn­the­sis of poly­sac­cha­rides, gly­col­ipids, and gly­co­pro­teins. In these reac­tions, UDP-Glc pro­vides glu­cose groups, trans­fer­ring them to accep­tor mol­e­cules to facil­i­tate com­plex car­bo­hy­drate structures.

Syn­the­sis of Cell Wall and Extra­cel­lu­lar Matrix
In plants, bac­te­ria, and oth­er organ­isms, UDP-Glc is involved in the syn­the­sis of cell wall com­po­nents such as cel­lu­lose and hemi­cel­lu­lose. This func­tion is cru­cial for main­tain­ing struc­tur­al integri­ty, enabling cells to sus­tain and rein­force their structure.

Reagent in Meta­bol­ic Path­way Research
In bio­chem­i­cal and phar­ma­co­log­i­cal research, UDP-Glc is wide­ly used to study car­bo­hy­drate metab­o­lism path­ways, includ­ing glyco­gen metab­o­lism and gly­co­sy­la­tion reac­tions in cel­lu­lar sig­nal­ing path­ways. It helps researchers inves­ti­gate key bio­chem­i­cal process­es and meta­bol­ic functions.

Pre­cur­sor in Drug Metab­o­lism
UDP-Glc also par­tic­i­pates in the metab­o­lism of cer­tain drugs, espe­cial­ly in the liv­er, where it facil­i­tates gly­co­sy­la­tion reac­tions that increase the water sol­u­bil­i­ty of drugs, mak­ing them eas­i­er to excrete from the body.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Cam­ing Phar­ma­ceu­ti­cal Lim­it­ed (http://​www​.cam​ing​.com/).

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