Fidaxomicin-d7

Catalog No.: A31071
Stable Isotope
Fidaxomicin-d7 is a deuterium-labeled derivative of Fidaxomicin, a macrocyclic antibiotic that acts as an inhibitor of RNA polymerase. This compound is primarily utilized in research to study the pharmacokinetics and metabolic pathways of Fidaxomicin, which exhibits potent activity against pathogenic Clostridium difficile while preserving the composition of the gut microbiota. Its stable isotope labeling facilitates advanced analytical studies in microbiological and pharmaceutical research contexts.
Grouped product items
Size Price Stock Qty
100µg
$320.00
In stock
Bulk Size
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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
DescriptionFidaxomicin-d7 is a deuterium-labeled derivative of Fidaxomicin, a macrocyclic antibiotic that acts as an inhibitor of RNA polymerase. This compound is primarily utilized in research to study the pharmacokinetics and metabolic pathways of Fidaxomicin, which exhibits potent activity against pathogenic Clostridium difficile while preserving the composition of the gut microbiota. Its stable isotope labeling facilitates advanced analytical studies in microbiological and pharmaceutical research contexts.
Product Information
Catalog NumA31071
FormulaC52H67D7Cl2O18
Molecular Weight1065.08
CAS Number2143934-06-7
SMILESC(O[C@H]1[C@H](O)[C@H](OC)[C@H](OC/C=2/C(=O)O[C@]([C@@H](C)O)(C/C=C(\C)/C=C(\C)/[C@H](O[C@H]3[C@@H](O)[C@@H](O)[C@H](OC(C(C([2H])([2H])[2H])(C([2H])([2H])[2H])[2H])=O)C(C)(C)O3)[C@@H](CC)/C=C(\C)/[C@@H](O)C/C=C/C2)[H])O[C@@H]1C)(=O)C4=C(CC)C(Cl)=C(O)C(Cl)=C4O
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