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D5782

2′,3′-Dideoxycytidine

≥98% (HPLC), synthetic (organic), powder

Sinónimos:

ddC

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Talla/SKUDisponibilidadPrecio
100 mg
Comprobar disponibilidad del carrito
US$ 221,00
250 mg
Comprobar disponibilidad del carrito
US$ 486,00
500 mg
Comprobar disponibilidad del carrito
US$ 873,00

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Fórmula empírica (notación de Hill):
C9H13N3O3
Número CAS:
Peso molecular:
211.22
NACRES:
NA.52
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
Beilstein/REAXYS Number:
654956
Assay:
≥98% (HPLC)
Biological source:
synthetic (organic)
Form:
powder
Solubility:
water: 50 mg/mL, clear, colorless to faintly yellow
Storage temp.:
−20°C

US$ 221,00

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Nombre del producto

2′,3′-Dideoxycytidine, ≥98% (HPLC)

biological source

synthetic (organic)

Quality Segment

assay

≥98% (HPLC)

form

powder

feature

PCR Additives

technique(s)

PCR: suitable, whole genome amplification: suitable

color

colorless

input

crude DNA

mp

217-218 °C (lit.)

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

NC1=NC(=O)N(C=C1)[C@H]2CC[C@@H](CO)O2

InChI

1S/C9H13N3O3/c10-7-3-4-12(9(14)11-7)8-2-1-6(5-13)15-8/h3-4,6,8,13H,1-2,5H2,(H2,10,11,14)/t6-,8+/m0/s1

InChI key

WREGKURFCTUGRC-POYBYMJQSA-N

Application

2′,3′-Dideoxycytidine is used:
  • as a DNA chain-terminating nucleotide for DNA sequencing methods based on the Sanger chain-termination method
  • as a nucleoside reverse transcriptase inhibitor (NRTI) to study its effects on the development of mechanical allodynia in aging mice
  • as a mitochondrial DNA (mtDNA) replication inhibitor to inhibit the activation of cGAS-STING pathway and study its effects on signaling protein-stimulator of interferon genes (STING), cyclic GMP-AMP synthase (cGAS), and phospho-interferon regulator factor 3 (p-IRF3) expression in mouse hippocampal and microglial cells
  • as an NRTI inhibitor to study its effects on the drug induced-mitochondrial toxicity in Caenorhabditis elegans

Biochem/physiol Actions

2′,3′-Dideoxycytidine (ddC), is an ionic compound and a nucleoside analog. It acts as a nucleoside reverse transcriptase inhibitor and exhibits therapeutic effects against human immunodeficiency virus (HIV) infection. 2′,3′-Dideoxycytidine possesses anti-adenovirus activity and inhibits the adenovirus polymerase.

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Este artículo
PHR3266E9386D3897
description

≥98% (HPLC)

description

pharmaceutical secondary standard, certified reference material

description

-

description

≥99% (HPLC)

biological source

synthetic (organic)

biological source

-

biological source

synthetic (organic)

biological source

synthetic (organic)

Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

200

assay

≥98% (HPLC)

assay

-

assay

≥95% (HPLC)

assay

≥99% (HPLC)

form

powder

form

-

form

powder

form

powder

storage temp.

−20°C

storage temp.

2-30°C

storage temp.

−20°C

storage temp.

−20°C

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

solubility

-

solubility

water: 50 mg/mL, clear, colorless to yellow

solubility

water: 50 mg/mL, clear, colorless to very faintly yellow


Pictogramas

Health hazard

Palabra de advertencia

Warning

Códigos de peligro

Indicaciones de precaución

Hazard Classifications

Carc. 2

Clase de almacenamiento

11 - Combustible Solids

¿Qué está pasando?

WGK 3

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable

EPI (equipos de protección individual)

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges



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Questions

  1. iS THIS TOXIN?

    1 answer
    1. This product is classified in the Globally Harmonized System as GHS08, which is a Health Hazard. Please see the link below to access the SDS:
      https://www.sigmaaldrich.com/documents-search?tab=sds

      To review the Hazard and Precautionary Statement, please see the link below:
      https://www.sigmaaldrich.com/life-science/safety/hazard-and-precautionary-statements#pictogram

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