2,3-Didehydro - 3 - deoxythymidine ,>=98% (TLC)

Code: d1413-50mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

2′,3′-Didehydro-3′-deoxythymidine has been used in cell treatment. It has also been used as a drug in Caenorhabditis elegansto study drug induced mitocho...


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Votre prix
$395.78 50MG

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

2′,3′-Didehydro-3′-deoxythymidine has been used in cell treatment. It has also been used as a drug in Caenorhabditis elegansto study drug induced mitochondrial toxicity. It has also been used in the preclinical evaluation of GS-9160.

Biochem/physiol Actions

2′,3′-Didehydro-3′-deoxythymidine is a nucleoside analog, which inhibits HIV replicationin vitro. Stavudine has the ability to enter the cells by non-facilitated diffusion. It possesses inhibitory activity against moloney murine leukemia virus, friend murine leukemia virus and simian immunodeficiency virus.

General description

2′,3′-Didehydro-3′-deoxythymidine (d4T), a pyrimidine analogue is the inhibitor of reverse transcriptase.

Other Notes

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. D1413.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Packaging

10, 50 mg in poly bottle

assay≥98% (TLC)
formpowder
InChI keyXNKLLVCARDGLGL-JGVFFNPUSA-N
InChI1S/C10H12N2O4/c1-6-4-12(10(15)11-9(6)14)8-3-2-7(5-13)16-8/h2-4,7-8,13H,5H2,1H3,(H,11,14,15)/t7-,8+/m0/s1
Quality Level200
SMILES stringCC1=CN([C@@H]2O[C@H](CO)C=C2)C(=O)NC1=O
storage temp.−20°C
Cas Number3056-17-5
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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