Bupranolol hydrochloride acts as a non-selective β-adrenergic receptor antagonist, exhibiting significant membrane-stabilizing properties. This compound is known to effectively modulate the contractile activity of the non-pregnant human uterus and has demonstrated impactful effects on spontaneous uterine contractions in in vitro studies involving ovarian cancer patients. Bupranolol hydrochloride is rapidly and completely absorbed in vivo, with carboxybupranolol identified as its primary metabolite, making it a valuable tool for research focused on adrenergic signaling and related pathophysiological conditions.
Bupranolol hydrochloride acts as a non-selective β-adrenergic receptor antagonist, exhibiting significant membrane-stabilizing properties. This compound is known to effectively modulate the contractile activity of the non-pregnant human uterus and has demonstrated impactful effects on spontaneous uterine contractions in in vitro studies involving ovarian cancer patients. Bupranolol hydrochloride is rapidly and completely absorbed in vivo, with carboxybupranolol identified as its primary metabolite, making it a valuable tool for research focused on adrenergic signaling and related pathophysiological conditions.
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