Bupranolol (Synonyms: (±)-Bupranolol) |
| カタログ番号GC62648 |
ブプラノロールは、固有の交感神経刺激活性を持たない、経口的に活性な競合的かつ非選択的なβ-アドレナリン受容体拮抗薬です。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 14556-46-8
Sample solution is provided at 25 µL, 10mM.
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Bupranolol is an orally active, competitive and non-selective β-adrenoceptor antagonist without intrinsic sympathomimetic activity[1].
Bupranolol (1~3 μM) shifts isoprenaline-induced relaxation in the presence of 30 μM propranolol. Bupranolol acts as a competitive antagonist of isoprenaline-induced relaxation in the presence of 300 nM propranolol, with a pA2 value of 5.90. Bupranolol antagonizes β1- and β2-ARs with pA2 values of ≈9.0, and also antagonizes β3-AR with a pA2 value of 6.0[1].
[1]. Chino D, et al. Pharmacological identification of β-adrenoceptor subtypes mediating isoprenaline-induced relaxation of guinea pig colonic longitudinal smooth muscle. J Smooth Muscle Res. 2018;54(0):13-27.
[2]. Babu RJ, et al. Effect of cyclodextrins on the complexation and transdermal delivery of bupranolol through rat skin. Int J Pharm. 2004;271(1-2):155-165.
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