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2′-Deoxycytidine

SIGMA/D3897 - ≥99% (HPLC)

Synonym: Cytosine deoxyriboside

CAS Number: 951-77-9
Empirical Formula (Hill Notation): C9H13N3O4
Molecular Weight: 227.22
EC Number: 213-454-1
MDL Number: MFCD00006547
Linear Formula: C9H13N3O4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-D3897-100MG 100 mg
$62.30
1/EA
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45-D3897-250MG 250 mg
$66.30
1/EA
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45-D3897-500MG 500 mg
$90.30
1/EA
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45-D3897-1G 1 g
$151.00
1/EA
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45-D3897-5G 5 g
$496.00
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D3897-100MG
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D3897-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D3897-250MG
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D3897-500MG
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: D3897-5G

 

assay ≥99% (HPLC)
biological source synthetic (organic)
form powder
InChI 1S/C9H13N3O4/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15)/t5-,6+,8+/m0/s1
InChI key CKTSBUTUHBMZGZ-SHYZEUOFSA-N
Quality Level 200 
SMILES string NC1=NC(=O)N(C=C1)[C@H]2C[C@H](O)[C@@H](CO)O2
solubility water: 50 mg/mL, clear, colorless to very faintly yellow
storage temp. −20°C
Application: 2′-Deoxycytidine has been used:
• as a substrate for Trypanosoma brucei cytidine deaminase (TbCDA) to measure its activity
• as a standard in the isolation and quantification of metabolite levels in murine tumor interstitial fluid by liquid chromatography-mass spectrometry (LC–MS)
• to study the role of autophagy in response to oncogenes and DNA replication stress

Biochem/physiol Actions: 2′-Deoxycytidine (deoxyC) forms dCTP upon phosphorylation which is used to synthesis DNA via various DNA polymerases or reverse transcriptases. DeoxyC is the substrate for deoxycytidine deaminase (EC 3.5.4.14) which converts it into 2′-deoxyuridine. DeoxyC is phosphorylated to the nucleotide dCMP by the enzyme deoxycytidine kinase (DCK). DeoxyC serves as a potential head and neck cancer marker.
General description: 2′-Deoxycytidine (deoxyC) is one of the deoxynucleosides containing cytosine as the nucleobase. It is found in the blood, feces, and urine.
Packaging: 1, 5 g in poly bottle
Packaging: 100, 250, 500 mg in poly bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥99% (HPLC)
Storage Temp. −20°C
UNSPSC 41106305

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