Informazioni sul prodotto
- Mabuterol, PB 868Cl
- 1-[4-Amino-3-Chloro-5-(Trifluoromethyl)Phenyl]-2-(Tert-Butylamino)Ethanol
- 4-Amino-3-chloro-α-[[(1,1-dimethylethyl)amino]methyl]-5-(trifluoromethyl)benzenemethanol
- 4-Amino-alpha-((tert-butylamino)methyl)-3-chloro-5-(trifluoromethyl)benzyl alcohol
- Ambuterol
- Benzenemethanol, 4-amino-3-chloro-alpha-(((1,1-dimethylethyl)amino)methyl)-5-(trifluoromethyl)-
- Benzenemethanol, 4-amino-3-chloro-α-[[(1,1-dimethylethyl)amino]methyl]-5-(trifluoromethyl)-
- Ccris 5288
- Mabuterol [INN]
- Mabuterolum
- Vedi altri sinonimi
- Mabuterolum [INN-Latin]
- PB 868Cl
- Unii-R4K19W6S7Q
Mabuterol is a selective agonist of β2 adrenoreceptor with no beta 1-stimulation. Mabuterol inhibited the positive inotropic effect of isoprenaline at 10(-7) g/ml and decreased the maximum driving frequency at 3 X 10(-6) g/ml. Mabuterol was 3 times more potent in relaxing the isolated rat uterus, but 700 times less potent than isoprenaline in relaxing the rabbit jejunum. Mabuterol (p.o.) depressed the intestinal propulsion and was equipotent to isoprenaline and 2.5 times less potent than salbutamol.
Proprietà chimiche
Richiesta tecnica su: TM-T27970 Mabuterol free base
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