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Merck

C1506

Sigma-Aldrich

Cytidine 5′-triphosphate disodium salt

≥95%

Sinónimos:

CTP

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About This Item

Fórmula empírica (notación de Hill):
C9H14N3Na2O14P3
Número de CAS:
Peso molecular:
527.12
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.77

Quality Level

assay

≥95%

form

powder

storage temp.

−20°C

SMILES string

[Na+].[Na+].NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](COP(O)(=O)OP([O-])(=O)OP(O)([O-])=O)[C@@H](O)[C@H]2O

InChI

1S/C9H16N3O14P3.2Na/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1

InChI key

NFQMDTRPCFJJND-WFIJOQBCSA-L

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Categorías relacionadas

General description

Cytidine 5′-triphosphate is a nucleoside triphosphate with a pyrimidine ring. It is present in RNA.

Application

Cytidine 5′-triphosphate disodium salt has been used:
  • for the conversion of adenosine monophosphate (AMP) to adenosine diphosphate (ADP) in luminometry analysis
  • in the preparation of ribonucleotide 5′-triphosphate precursors stocks for large-scale RNA synthesis
  • to perform in vitro transcription

Biochem/physiol Actions

Cytidine 5′-triphosphate (CTP) prevents the action of aspartate carbamoyltransferase. This enzyme participates in pyrimidine biosynthesis. Like adenosine triphosphate (ATP), CTP serves as a molecule of high energy. It acts as a coenzyme in glycerophospholipid biosynthesis and protein glycosylation.
P2X4 purinergic receptor agonist.

Features and Benefits

This compound is featured on the P2 Receptors: P2X Ion Channel Family page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Determining structures of RNA aptamers and riboswitches by X-ray crystallography
Nucleosides, nucleotides & nucleic acids, 135-163 (2009)
Andrea L Edwards et al.
Methods in molecular biology (Clifton, N.J.), 535, 135-163 (2009-04-21)
Structural biology plays a central role in gaining a full understanding of the myriad roles of RNA in biology. In recent years, innovative approaches in RNA purification and crystallographic methods have lead to the visualization of an increasing number of
Methods in Molecular Biology, 89-89 (2018)
Secretion From Dense Granules
Platelets and megakaryocytes, 83-93 (2004)
Genetics (2016)

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