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Merck

C9755

Sigma-Aldrich

Cytidine 5′-diphosphate sodium salt hydrate

from yeast, ≥95%

Sinónimos:

CDP sodium salt hydrate

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About This Item

Fórmula empírica (notación de Hill):
C9H15N3O11P2
Peso molecular:
403.18
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.51

biological source

yeast

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

Categorías relacionadas

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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Visite la Librería de documentos

Yan Zhang et al.
Biochemistry, 50(25), 5615-5623 (2011-05-13)
Bacillus subtilis class Ib ribonucleotide reductase (RNR) catalyzes the conversion of nucleotides to deoxynucleotides, providing the building blocks for DNA replication and repair. It is composed of two proteins: α (NrdE) and β (NrdF). β contains the metallo-cofactor, essential for
Microglial cells in the retina of Carassius auratus: effects of optic nerve crush
Salvador-Silva M, et al.
The Journal of Comparative Neurology, 417(4), 431-447 (2000)
CTP synthetase and its role in phospholipid synthesis in the yeast Saccharomyces cerevisiae
Chang YF and Carman GM
Progress in Lipid Research, 47(5), 333-339 (2008)
Ribonucleotide reductase requires subunit switching in hypoxia to maintain DNA replication
Foskolou IP, et al.
Molecular Cell, 66(2), 206-220 (2017)
Purine and pyrimidine nucleotide synthesis and metabolism
The Arabidopsis Book / American Society of Plant Biologists, 1 (2002)

Protocolos

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

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

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

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

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