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Isoproterenol hydrochloride

Isoproterenol. Isoproterenol hydrochloride is an nonselective P-adrenoceptor agonist that is chemically related to NE. It mimics the effects of stimulation of the sympathetic innervation to the heart which are mediated by NE. It increases heart rate by increasing automaticity of the SA and AV nodes by increasing the rate of phase 4 diastoHc depolarization. It is used in the treatment of acute heart block and supraventricular bradyarrhythmias, although use of atropine is safer for bradyarrhythmias foUowing MI (86). [Pg.120]

FIG. 17 Chemical structures of (a) epinephrine hydrochloride, (b) dopamine hydrochloride, (c) isoproterenol hydrochloride, (d) phenylephrine hydrochloride, (e) tolazoline hydrochloride, (f) oxyprenolol hydrochloride, (g) alprenolol hydrochloride, and (h) propranolol hydrochloride. [Pg.714]

Injection (1 5000 solution) 0.2 mg/mL (Rx) Isoproterenol Hydrochloride (ESI Lederle), /swpre/(Abbott)... [Pg.707]

Beta-adrenergic agonists, nonselecitve isoproterenol hydrochloride orciprenaline sulfate... [Pg.623]

Isopto Atropine atropine, isoprenaline [ban. inn] (Isopropylnorepinephrine isoproterenol hydrochloride [usan] Isuprel etc. isoproterenol sulfate [usan] Aludrin Medihaler-lso ) is a P-adrenoceptor AGONIST which therapeutically can be used as a bronchodilator in antiasthmatic treatment. The (f )-form is levisoprenaline [inn]. isopropamide iodide [ban. inn] is a quaternary ammonium MUSCARINIC CHOUNOCEPTOR ANTAGONIST, which can be used as a visceral ANTISPASMODIC and as an adjunct in treating peptic ulcers. [Pg.157]

ISOPROTERENOL HYDROCHLORIDE (Isuprel, Isuprel Mistometer, Norisodrine)... [Pg.364]

Dihydroxy-a-[(isopropylamino) methyl] benzyl alcohol hydrochloride 1, 2-Benzenediol, 4-[1-hydroxy-2-[(methyl-ethyl)-amino] ethyl]-, hydrochloride Isoprenaline Hydrochloride BP Int. P., Isoproterenol Hydrochloride USP ... [Pg.377]

Isoproterenol hydrochloride undergoes appreciable o-methylation by the aid of catechol-o-methyl transferase (COMT) in the humans. One may also observe a striking and pronounced identical structural features between isoprenaline and the endogenous catecholamines, namely dopamine and norepinephrine (NE). [Pg.384]

Permeability coefficients in this article are different from permeabihty coefficients in another related article (Hatanaka et al., 1990) because different hairless rat strains were used. The permeabihty coefficients for diclofenac sodium, dopamine hydrochloride, isoproterenol hydrochloride, indomethadn, and water were reported in the... [Pg.359]

A. Parenteral. Isoproterenol hydrochloride (Isuprel, others), 20 mcg/mL (1 50,000) or 200 mcg/mL (1 5,000), which contains sodium bisulfite or sodium metabisulfite as a preservative. [Pg.459]

Figure 11 Chromatogram of the imprinted stationary phase. This imprinted polymer does work in aqueous solvents and chromatographic characterizations are performed using an aqueous mobile phase (25 mM sodium citrate, pH 3.0) containing 10% MeCN at a flow rate of 1 mL/min and chromatograms, run in isocratic mode and recorded at 280 nm. Injections of 20 luL of 2 mM racemic isoproterenol HCl (40 pmol) dissolved in the mobile phase are done in order to evaluate the enantioselectivity towards its imprinted print molecule isoproterenol. Eluent used was a sodium citrate buffer (pH 3.0, 25 mM citrate, 10% MeCN) flow rate 1 ml/min, peak detection at 280 nm, injection of 20 pL of a racemic isoproterenol hydrochloride solution (2 mM), acetone was used as void marker. The structures of + and - isoproterenol are given in Fig. 8. Figure 11 Chromatogram of the imprinted stationary phase. This imprinted polymer does work in aqueous solvents and chromatographic characterizations are performed using an aqueous mobile phase (25 mM sodium citrate, pH 3.0) containing 10% MeCN at a flow rate of 1 mL/min and chromatograms, run in isocratic mode and recorded at 280 nm. Injections of 20 luL of 2 mM racemic isoproterenol HCl (40 pmol) dissolved in the mobile phase are done in order to evaluate the enantioselectivity towards its imprinted print molecule isoproterenol. Eluent used was a sodium citrate buffer (pH 3.0, 25 mM citrate, 10% MeCN) flow rate 1 ml/min, peak detection at 280 nm, injection of 20 pL of a racemic isoproterenol hydrochloride solution (2 mM), acetone was used as void marker. The structures of + and - isoproterenol are given in Fig. 8.
Hydroxypropylcellulose has been used for the development of a peroral controlled-release dosage form of isoproterenol hydrochloride. ... [Pg.544]

Isoproterenol hydrochloride P-Adrenergic agonist 8 C3 128701/15771 82202/15441 2.753 pckl+hit compound... [Pg.162]

See other pages where Isoproterenol hydrochloride is mentioned: [Pg.533]    [Pg.118]    [Pg.713]    [Pg.410]    [Pg.1053]    [Pg.707]    [Pg.708]    [Pg.770]    [Pg.652]    [Pg.533]    [Pg.367]    [Pg.383]    [Pg.689]    [Pg.499]    [Pg.507]    [Pg.157]    [Pg.916]    [Pg.715]    [Pg.377]    [Pg.240]    [Pg.392]    [Pg.158]    [Pg.25]   
See also in sourсe #XX -- [ Pg.652 ]

See also in sourсe #XX -- [ Pg.689 ]

See also in sourсe #XX -- [ Pg.377 , Pg.378 , Pg.384 ]

See also in sourсe #XX -- [ Pg.240 ]

See also in sourсe #XX -- [ Pg.25 ]



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Isoproterenol

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