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C9755

Sigma-Aldrich

Cytidine 5′-diphosphate sodium salt hydrate

from yeast, ≥95%

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Synonym(s):
CDP sodium salt hydrate
Empirical Formula (Hill Notation):
C9H15N3O11P2
Molecular Weight:
403.18
MDL number:
PubChem Substance ID:
NACRES:
NA.51

biological source

yeast

Quality Level

assay

≥95%

form

powder

storage temp.

−20°C

SMILES string

[Na].NC1=NC(=O)N(C=C1)C2OC(COP(O)(=O)OP(O)(O)=O)C(O)C2O

InChI

1S/C9H15N3O11P2.Na.H/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H2,10,11,15)(H2,16,17,18);;

InChI key

MAGSIBHRUIBONY-UHFFFAOYSA-N

Related Categories

General description

Cytidine 5′-diphosphate (CDP) is synthesized from cytidine monophosphate (CMP) or uridine monophosphate (UMP) by the transfer of phosphoryl group, catalyzed by the enzyme uridylate kinase (UMPK). CTP synthetase catalyzes the conversion of CTP to CDP intermediates like CDP-diacylglycerol, CDP-choline and CDP-ethanolamine for phospholipid biosynthesis.

Application

Cytidine 5′-diphosphate sodium salt hydrate has been used:
  • as a substrate in nucleoside diphosphatase (NDPase) enzyme histochemistry assay of gold fish eye sections
  • in ribonucleotide reductase assay
  • dCDP formation assay.

Biochem/physiol Actions

Cytidine 5′-diphosphate (CDP) is used as a substrate of nucleoside diphosphatase kinase to produce CTP for supporting DNA and RNA biosynthesis and of ribonucleotide reductase to product dCMP.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

Eyeshields, Gloves, type N95 (US)


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Protocols

ZIC®-cHILIC is a densely bonded zwitterionic stationary phase with phosphorylcholine functional groups covalently attached to silica.

HILIC separation is an alternative that permits sensitive MS detection and without the use of ion-pair reagents.

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