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Spinosyn A

Catalog No.: B11549
Insecticide
Spinosyn A is a macrolide insecticide derived from the fermentation of Saccharopolyspora spinosa. It primarily targets the nicotinic acetylcholine receptor and exhibits high potency against a range of pest species. This compound is widely utilized in integrated pest management strategies due to its effectiveness and selective toxicity, making it valuable for agricultural applications.
Spinosyn A 131929-60-7 Insecticide
Grouped product items
Size Price Stock Qty
1mg
$140.00
In stock
2mg
$215.00
In stock
5mg
$360.00
In stock
10mg
$495.00
In stock
25mg
$770.00
In stock
50mg
$970.00
In stock
100mg
$1,330.00
In stock
200mg
$1,755.00
In stock
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Free Delivery on orders over $500
Research use only. We do not sell to patients.
Data Sheet SDS

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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
DescriptionSpinosyn A is a macrolide insecticide derived from the fermentation of Saccharopolyspora spinosa. It primarily targets the nicotinic acetylcholine receptor and exhibits high potency against a range of pest species. This compound is widely utilized in integrated pest management strategies due to its effectiveness and selective toxicity, making it valuable for agricultural applications.
Product Information
Catalog NumB11549
FormulaC41H65NO10
Molecular Weight731.96
CAS Number131929-60-7
SMILESO=C([C@@H]([C@H](CCC[C@@H](O1)CC)O[C@@H]2O[C@@H]([C@H](CC2)N(C)C)C)C)C3=C[C@@]([C@](C=C[C@]4([H])C5)([H])[C@]3([H])CC1=O)([H])[C@]4([H])C[C@@H]5O[C@H]6[C@@H]([C@@H]([C@H]([C@@H](O6)C)OC)OC)OC
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