Sulfoxaflor
CAS No. 946578-00-3
Sulfoxaflor( GF 2032 | GF 2372 | XDE 208 )
Catalog No. M27197 CAS No. 946578-00-3
Sulfoxaflor, an agonist of nAChR1 and nAChR2 subtypes, is a systemic insecticide that acts on the central nervous system of insects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 259 | Get Quote |
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| 5MG | 291 | Get Quote |
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| 10MG | 406 | Get Quote |
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| 25MG | 604 | Get Quote |
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| 50MG | 806 | Get Quote |
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| 100MG | 1051 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameSulfoxaflor
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NoteResearch use only, not for human use.
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Brief DescriptionSulfoxaflor, an agonist of nAChR1 and nAChR2 subtypes, is a systemic insecticide that acts on the central nervous system of insects.
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DescriptionSulfoxaflor, an agonist of nAChR1 and nAChR2 subtypes, is a systemic insecticide that acts on the central nervous system of insects. Sulfoxaflor is used for the control of sap-feeding insects such as Nilaparvata lugens, Bemissia tabaci, Myzus persicae, an
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In Vitro——
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In Vivo——
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SynonymsGF 2032 | GF 2372 | XDE 208
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PathwayCell Cycle/DNA Damage
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TargetAChR
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Recptorγ-secretase
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Research Area——
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Indication——
Chemical Information
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CAS Number946578-00-3
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Formula Weight277.27
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Molecular FormulaC10H10F3N3OS
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(c1ccc(nc1)C(F)(F)F)S(C)(=O)=NC#N
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Garcinone C
Garcinone C is a xanthone derivative extracted from Garcinia oblongifolia Champ with anti-inflammatory, astringency, and granulation-promoting activities. Garcinone C is an AChE inhibitor and has potential cytotoxic effects on certain cancers.
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10-Gingerol
10-Gingerol-induced apoptosis was accompanied by phosphorylation of the mitogen-activated protein kinase (MAPKs) family, p38 MAPK (p38), c-Jun N-terminal kinase (JNK), and extracellular signal-regulated kinase (ERK).
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TC-T 6000
TC-T 6000 (hENT4-IN-1) is a selective and potent inhibitor of human equilibrium nucleoside transporter protein 4 (ENT4) (IC50: 74.4 nM) with vasodilator activity, inhibits hENT1 and hENT2, and can be used for the study of cancer and cardiovascular injury.
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