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& Salzberg, S

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Pharmacokinetic profiles for the compound place its plasma half-life in the neighborhood of 45 minutes after parenteral administration in animal models, which informs typical dosing intervals in published experiments

n = 8), while a second group received 5A-1MQ treatment at 32 mg/kg of active pharmaceutical ingredient (injections of 4 mg 5A-1MQ monochloride salt/mL sterile saline dosed at 10 mL/kg body weight) after being switched from WD to LD (termed the WD/LD-T group