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(±)-CP 55,940-d11

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    (±)-CP 55,940-d<sub>11</sub>
  • (±)-CP 55,940-d<sub>11</sub>
Cat No: 10703
Biochemicals - Isotopically Labeled Standards
Cayman
Price is excluding VAT and does not include packaging neither shipping

(±)-CP 55,940-d11 is intended for use as an internal standard for the quantification of (±)-CP 55,940 (Item No. 13241) by GC- or LC-MS. (±)-CP 55,940 is a potent, non-selective cannabinoid (CB) receptor agonist (Kis = 5 and 1.8 nM for human CB1 and CB...

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Territorial Availability: Available through Bertin Pharma only in Europe
Special Advice: regulated item by French Administration ANSM / special delivery time and additional fees.
Synonyms:
  • rel-5-(1,1-dimethylheptyl-3,3,4,4,5,5,6,6,7,7,7-d11)-2-[(1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]-phenol
Correlated keywords:
  • deuterated deuterium GCMS LCMS analgetic THC thermal mechanical cannabimimetic CP55940 55940 cb
Product Overview:
(±)-CP 55,940-d11 is intended for use as an internal standard for the quantification of (±)-CP 55,940 (Item No. 13241) by GC- or LC-MS. (±)-CP 55,940 is a potent, non-selective cannabinoid (CB) receptor agonist (Kis = 5 and 1.8 nM for human CB1 and CB2, respectively).{7912} It stimulates [35S]GTPγS binding to rat cerebellar membranes (EC50s = 0.22-0.96 nM).{41807} In vivo, (±)-CP 55,940 induces analgesia in the tail clamp, hot plate, tail flick, flinch jump, and PBQ-induced writhing tests with 50% maximum possible effect (MPE50) values of 0.46, 1.11, 0.55, 0.63, and 0.29 mg/kg, respectively.{6752} (±)-CP 55,940 also decreases the discrimination index (DI) of female, but not male, rats in the object location task as well as the DI of male, but not female, rats in the novel object recognition task.{41808}
Size 1 mg
Shipping dry ice
Stability Store at -20 degrees; shelf life 365 days
Molecular Formula C24H29D11O3
SMILES O[C@H]1C[C@@H](C2=CC=C(C(C)(C)CC([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])C=C2O)[C@H](CCCO)CC1
Molecular Weight 387,6
Formulation A solution in methanol
Purity ≥99% deuterated forms (d1-d11)
Custom Code 2907.19
UNSPSC code 12352100

Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

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.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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