Tiamulin-d10-1 hydrochloride

Catalog No.: A47336
Stable Isotope
Tiamulin-d10-1 hydrochloride is a deuterium-labeled derivative of the diterpenic antibiotic Tiamulin. Its primary mechanism targets bacterial protein synthesis, making it crucial in research involving infectious diseases in livestock, particularly in the control of Mycoplasma spp. Tiamulin is commonly utilized in studies of airsacculitis, facilitating enhanced understanding of antibiotic efficacy and resistance mechanisms in veterinary medicine.
Grouped product items
Size Price Stock Qty
500µg
$435.00
In stock
1mg
$695.00
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
DescriptionTiamulin-d10-1 hydrochloride is a deuterium-labeled derivative of the diterpenic antibiotic Tiamulin. Its primary mechanism targets bacterial protein synthesis, making it crucial in research involving infectious diseases in livestock, particularly in the control of Mycoplasma spp. Tiamulin is commonly utilized in studies of airsacculitis, facilitating enhanced understanding of antibiotic efficacy and resistance mechanisms in veterinary medicine.
Product Information
Catalog NumA47336
FormulaC28H38D10ClNO4S
Molecular Weight540.26
CAS Number2750534-93-9
SMILESC[C@@H]1[C@]23[C@](C(CC3)=O)([H])[C@@]([C@@H](C[C@](C)([C@H]1O)C=C)OC(CSCCN(C([2H])([2H])C([2H])([2H])[2H])C([2H])([2H])C([2H])([2H])[2H])=O)([C@@H](CC2)C)C.Cl
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