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ST 91 is an agonist of α2-adrenergic receptors (α2-ARs).1 It induces cAMP accumulation in HEK293 cells expressing α2A-, α2B-, or α2C-ARs (EC50s = 155, 371, and 851 nM, respectively). ST 91 (100 nM) inhibits isoproterenol-induced relaxation in phenylephrine-precontracted isolated rat mesenteric arterial rings.2 Intrathecal administration of ST 91 (10 and 30 µg/animal) reduces paw flinching in the first and second phases of the formalin test in rats.3 It increases plasma atrial natriuretic peptide (ANP) levels, urinary output, and sodium, potassium, and cGMP excretion in conscious rats when administered at a dose of 250 µg/animal.4
WARNING This product is not for human or veterinary use.
1. Ligand efficacy and potency at recombinant α2 adrenergic receptors: Agonist-
2. α2B-
3. Dexmedetomidine and ST-
4. The peripheral action of clonidine analog ST-