Glyphosate-13C

Catalog No.: A31346
Stable Isotope
Glyphosate-13C is a stable isotope-labeled form of glyphosate, a non-selective systemic herbicide that targets the 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) within the shikimic acid pathway. By inhibiting EPSPS, glyphosate effectively disrupts the synthesis of key aromatic amino acids, including tyrosine, phenylalanine, and tryptophan. Its biological activity includes the induction of oxidative stress and neuroinflammation, which can lead to mitochondrial dysfunction and neuronal cell death through autophagy or apoptosis. This compound is useful in research applications related to herbicide metabolism, environmental impact studies, and understanding the neurotoxic effects associated with glyphosate exposure.
Grouped product items
Size Price Stock Qty
5mg
$410.00
In stock
10mg
$680.00
In stock
25mg
$1,360.00
In stock
50mg
$2,130.00
In stock
100mg
$3,320.00
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)
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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
DescriptionGlyphosate-13C is a stable isotope-labeled form of glyphosate, a non-selective systemic herbicide that targets the 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) within the shikimic acid pathway. By inhibiting EPSPS, glyphosate effectively disrupts the synthesis of key aromatic amino acids, including tyrosine, phenylalanine, and tryptophan. Its biological activity includes the induction of oxidative stress and neuroinflammation, which can lead to mitochondrial dysfunction and neuronal cell death through autophagy or apoptosis. This compound is useful in research applications related to herbicide metabolism, environmental impact studies, and understanding the neurotoxic effects associated with glyphosate exposure.
Product Information
Catalog NumA31346
FormulaC213CH8NO5P
Molecular Weight170.07
CAS Number287399-31-9
SMILESOC([13CH2]NCP(O)(O)=O)=O
Useful Calculator

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Mass (mg) = Concentration (mM) × Volume (mL) × Molecular Weight (g/mol)

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