Capecitabine-d11

Catalog No.: A30893
Stable Isotope
Capecitabine-d11 is a deuterium-labeled derivative of Capecitabine, an oral prodrug that is metabolically converted to the active compound 5-fluorouracil (5-FU) by thymidine phosphorylase. This stable isotope variant enables the study of drug metabolism and pharmacokinetics within biological systems, making it a valuable tool in cancer research and therapeutic monitoring. Researchers can utilize Capecitabine-d11 to enhance the specificity and accuracy of metabolic studies involving 5-FU.
Grouped product items
Size Price Stock Qty
1mg
$230.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionCapecitabine-d11 is a deuterium-labeled derivative of Capecitabine, an oral prodrug that is metabolically converted to the active compound 5-fluorouracil (5-FU) by thymidine phosphorylase. This stable isotope variant enables the study of drug metabolism and pharmacokinetics within biological systems, making it a valuable tool in cancer research and therapeutic monitoring. Researchers can utilize Capecitabine-d11 to enhance the specificity and accuracy of metabolic studies involving 5-FU.
Product Information
Catalog NumA30893
FormulaC15H11D11FN3O6
Molecular Weight370.42
CAS Number1132662-08-8
SMILESC[C@@H]1[C@H]([C@H]([C@H](N2C(N=C(C(F)=C2)NC(OC([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])=O)=O)O1)O)O
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