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Dexmedetomidine is an agonist of alpha2-adrenergic receptors (alpha2-ARs). It selectively binds to alpha2-ARs over alpha1-ARs (Kis = 0.015 and 5 nM, respectively). In vivo, dexmedetomidine (50 µg/kg) prevents increases in cardiac troponin I (CTnI), a marker of myocardial injury, as well as reduces myocardial apoptosis, pyroptosis, and ferroptosis in a mouse model of sepsis induced by cecal ligation and puncture (CLP), effects that can be reversed by the alpha2-AR antagonist yohimbine (Cay-19869). Dexmedetomidine (40 µg/kg) induces sedation and decreases mechanical nociception in cats. Formulations containing dexmedetomidine have been used as sedatives. This product is also available as an analytical reference standard (Cay-38806).Formal Name: 5-[(1S)-1-(2,3-dimethylphenyl)ethyl]-1H-imidazole. CAS Number: 113775-47-6. Synonyms: MPV 1440. Molecular Formula: C13H16N2. Formula Weight: 200.3. Purity: >98%. Formulation: (Request formulation change), A solid. Solubility: Acetonitrile: Slightly soluble, DMSO: Soluble, Water: Slightly soluble. SMILES: CC1=C(C)C([C@H](C)C2=CN=CN2)=CC=C1. InChi Code: InChI=1S/C13H16N2/c1-9-5-4-6-12(10(9)2)11(3)13-7-14-8-15-13/h4-8,11H,1-3H3,(H,14,15)/t11-/m0/s1. InChi Key: CUHVIMMYOGQXCV-NSHDSACASA-N.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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