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AM2201 N-(3-fluoropentyl) isomer

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    AM2201 N-<wbr/>(3-<wbr/>fluoropentyl) isomer
  • AM2201 N-<wbr/>(3-<wbr/>fluoropentyl) isomer
Cat No: 9001030
Biochemicals - Analytical Standards
Cayman

AM2201 is a potent synthetic cannabinoid (CB) with Ki values of 1.0 and 2.6 nM for the central cannabinoid (CB1) and the peripheral cannabinoid (CB2) receptors, respectively.{18696} AM2201 N-(3-fluoropentyl) isomer differs structurally from AM2201 by h...

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Territorial Availability: Available through Bertin Technologies only in France
Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.
Special Advice: Please check regulation status before ordering; additionel fees can apply.
Synonyms:
  • (1-(3-fluoropentyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone
Correlated keywords:
  • forensics AM-2201 AM 2201 isomers cannabinoids CBs receptors pain CBs CB1 CB2 analytical references standards 2201am
Product Overview:
AM2201 is a potent synthetic cannabinoid (CB) with Ki values of 1.0 and 2.6 nM for the central cannabinoid (CB1) and the peripheral cannabinoid (CB2) receptors, respectively.{18696} AM2201 N-(3-fluoropentyl) isomer differs structurally from AM2201 by having a fluoro atom at the 3 position rather than the 5 position of the pentyl chain. The physiological and toxicological properties of this compound have not been reported. This product is intended for forensic applications.
Size 100 µg
Shipping dry ice
Molecular Formula C24H22FNO
SMILES CCC(F)CCN1C=C(C(C2=CC=CC3=C2C=CC=C3)=O)C4=CC=CC=C41
Molecular Weight 359,4
Formulation A solution in methanol
Purity ≥98%
Custom Code 3822.19
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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