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Spinosad

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    Spinosad
  • Spinosad
Cat No: 25649
Biochemicals - Ion Channel Modulation
Cayman

Spinosad is a naturally-occurring insecticide found in the the soil bacterium S. spinosa.{26995} It is a mixture of the macrocyclic lactones spinosyn A (Item No. 16528) and spinosyn D (Item No. 19158), which act as agonists of insect nicotinic acetylc...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • spinosyn A and D (mixture)
Correlated keywords:
  • 187473-56-9 251304-69-5 937365-79-2 2072821-83-9 Saccharopolyspora Ceratitis Pgp Blackhawk Comfortis Conserve Entrust WP Extinosad GF-120 GF120 Fruit Fly Bait NF Naturalyte 1587 GF1587 Gardens Alive Bulls-Eye LY-232105 XDE105 Laser Naturalure PP-105 PP105 SpinTor Spinoace 45% SC 45SC NT Spinosads Success 4 Tracer Bactrocera
Product Overview:
Spinosad is a naturally-occurring insecticide found in the the soil bacterium S. spinosa.{26995} It is a mixture of the macrocyclic lactones spinosyn A (Item No. 16528) and spinosyn D (Item No. 19158), which act as agonists of insect nicotinic acetylcholinesterase receptors (nAChRs). Oral administration of spinosad induces toxicity in fruit flies including C. capitata, B. curcurbitae, and B. dorsalis (LC50s = 2.8-4.2, 4.3-5.5, and 3.1-3.3 µg/ml, respectively) but has low toxicity in vertebrates.{39930,42230,26996} It also inhibits canine P-glycoprotein (P-gp; IC50 = 0.2 µg/ml).{39931} Formulations containing spinosad have been used in the agricultural and veterinary control of insects.
Size 5 mg
Shipping dry ice
CAS Number 168316-95-8
Molecular Formula C83H132N2O20
SMILES CN(C)[C@H]1CC[C@@](O[C@H]([C@@H](C)C2=O)CCC[C@H](CC)OC(C[C@]3([H])C2=C[C@]4([H])[C@@]3([H])C=C[C@@]5([H])[C@@]4([H])C[C@H](O[C@]6([H])O[C@@H](C)[C@H](OC)[C@@H](OC)[C@H]6OC)C5)=O)([H])O[C@@H]1C.CN(C)[C@H]7CC[C@@](O[C@H]([C@@H](C)C8=O)CCC[C@H](CC)OC(C[C@]9(
Molecular Weight 1478
Formulation A solid
Purity ≥95%
Custom Code 2932.99
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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