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Merck

C4654

Sigma-Aldrich

Cytidine

BioReagent, suitable for cell culture, powder, ≥99%

Sinónimos:

Cytosine β-D-riboside, Cytosine-1-β-D-ribofuranoside

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About This Item

Fórmula empírica (notación de Hill):
C9H13N3O5
Número de CAS:
Peso molecular:
243.22
Beilstein:
89173
Número CE:
Número MDL:
Código UNSPSC:
12352207
ID de la sustancia en PubChem:
NACRES:
NA.75

origen biológico

synthetic

Línea del producto

BioReagent

Análisis

≥99%

formulario

powder

técnicas

cell culture | mammalian: suitable

mp

210-220 °C (dec.) (lit.)

solubilidad

H2O: 50 mg/mL

cadena SMILES

NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O

InChI

1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7-,8-/m1/s1

Clave InChI

UHDGCWIWMRVCDJ-XVFCMESISA-N

Información sobre el gen

mouse ... Uck1(22245)

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Descripción general

Cytidine is a nucleoside molecule. It is formed when cytosine is attached to a ribose ring through a β-N1-glycosidic bond.

Aplicación

Cytidine has been used as a component to prepare ribonucleoside stock solution to assess its effects on the anaerobic growth of several Bacillus mojavensis strains.
Cytidine has been used as a non-essential aminoacid component of minimal essential medium (MEM) to analyse interspecies somatic cell nucleus transfer (iSCNT)-derived blastocysts. It has also been used as a supplement in the culture medium of HeLa cells, to study the effects of cytidine addition on rods and rings (RR) induced by glutamine deprivation.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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