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Amobarbital

Ammonium ion, JV-(2-thenyl)-N-benzyldimethyl-Stevens and Sommelet rearrangement, 4, 800 Ammonium salts, diallyldialkyl-polymerization, 1, 293 Ammonium salts, 2-pyrrolylmethyl-nucleophilic substitution abnormal, 4, 244 Sommelet rearrangement, 4, 244 Ammonium salts, trimethyl(l,3,5-triazinyl)-applications, 3, 525 Amobarbital, 3, 150 Amodiaquine, 1, 145 Amolanone applications, 4, 708... [Pg.515]

Figure 11.19 SPME-CE analysis of urine samples (a) blank urine (a) directly injected and extracted for (b) 5 (c) 10 and (d) 30 min (b) Urine spiked with barbiturates, extracted for (e) 30 and (f, g) 5 min. Peak identification is as follows 1, pentobaitibal 2, butabarbital 3, secobarbital 4, amobarbital 5, aprobarbital 6, mephobarbital 7, butalbital 8, thiopental. Concenti ations used are 0.15-1.0 ppm (e, f) and 0.05-0.3 ppm (g). Reprinted from Analytical Chemistry, 69, S. Li and S. G. Weber, Determination of barbiturates by solid-phase microexti action and capillary electrophoresis, pp. 1217-1222, copyright 1997, with permission from the American Chemical Society. Figure 11.19 SPME-CE analysis of urine samples (a) blank urine (a) directly injected and extracted for (b) 5 (c) 10 and (d) 30 min (b) Urine spiked with barbiturates, extracted for (e) 30 and (f, g) 5 min. Peak identification is as follows 1, pentobaitibal 2, butabarbital 3, secobarbital 4, amobarbital 5, aprobarbital 6, mephobarbital 7, butalbital 8, thiopental. Concenti ations used are 0.15-1.0 ppm (e, f) and 0.05-0.3 ppm (g). Reprinted from Analytical Chemistry, 69, S. Li and S. G. Weber, Determination of barbiturates by solid-phase microexti action and capillary electrophoresis, pp. 1217-1222, copyright 1997, with permission from the American Chemical Society.
Intermediate-acting (eg, amobarbital [Amytal], aprobarbital [Alurate], butabarbital [Butisol]). The average duration of action of die intermediate-acting barbiturates is 6 to 8 hours. [Pg.237]

Respiratory and central nervous system depression, nausea, vomiting, constipation, diarrhea, bradycardia, hypotension, syncope, hypersensitivity reactions, headache Same as amobarbital sodium... [Pg.238]

Sedative and Hypnotic Combinations Tuinal—amobarbital, secobarbitol... [Pg.683]

Carlytene amobarbital Visc6ralgine comprimes TXiinal (Lilly)... [Pg.101]

C2H5Br 74-96-4) see Actinoquinol Amobarbital Benzilonium bromide Cyclobarbital Edrophonium chloride Heptabarb Mephenytoin Methylphenobarbital Norfloxacin Oxitropium bromide Phenobarbital Remoxipride Secbutabaibital Valdetamide ethyl bromoacetate... [Pg.2376]

CH4N2O 57-13-6) see Alfuzosin Allantoin Amobarbital Barbital Bromisoval Butalbital Carbasalate calcium Carbromal Cyclopentobarbital Dimethadione Dipyridamole Enoximone Ethotoin Heptabarb Metaxalone Methyclothiazide Orotic acid Paramethadione Pentobarbital Phenacemide Phenetuiide Phenobarbital Phenytoin Proquazone Secbutabarbital Secobarbital Sulfadimethoxine Thalidomide Trimethadione... [Pg.2453]

Intermediate acting Amobarbital Amytal, Tuinal (with secobarbital)... [Pg.139]

The ultra-short-acting barbiturates include methohexital sodium (Brevi-tal) and thiopental sodium (Pentothal). These agents are used as anesthetics and are administered intravenously. Barbiturates with short-to-intermediate duration of action are used for their sedative-hypnotic effect in the treatment of anxiety. These medications include amobarbital (Amytal), butabarbital (Butisol), sodium pentobarbital (Nembutal), and secobarbital (Seconal). [Pg.139]

Barbiturates such as amobarbital inhibit NAD-hnked dehydrogenases by blocking the transfer from FeS to Q. At sufficient dosage, they are fatal in vivo. Antin cin A and dimercaprol inhibit the respiratory chain between cytochrome b and cytochrome c. The classic poisons H2S, carbon monoxide, and cyanide inhibit cytochrome oxidase and can therefore totally arrest respiration. Malonate is a competitive inhibitor of succinate dehydrogenase. [Pg.95]

In this study, potential oscillation was measured in the presence of lOOmM sodium salts of barbital, allobarbital, phenobarbital, and amobarbital in phase wl [19]. Their chemical structures are shown in Fig. 15. Amplitude and the oscillatory and induction periods were noted to depend on the particular hypnotic used. Amplitude decreased in the order, barbital > allobarbital > phenobarbital > amobarbital. The oscillatory period increased in the order, barbital < allobarbital < phenobarbital < amobarbital. Induction period increased in the order, barbital < allobarbital < phenobarbital < amobarbital. These parameters changed depending on drug concentration. Hypnotics at less than 5 mM had virtually no effect on the oscillation mode. [Pg.712]

FIG. 15 Chemical structures of (a) sodium barbital, (b) sodium allobarbital, (c) sodium phenobarbital, and (d) sodium amobarbital. [Pg.712]

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