Protriptyline

If the peaks for fluoxetine and protriptyline are insufficiently resolved, how might you alter the mobile phase to improve their separation ... [Pg.589]

Protozoa Protozoacide Protozoal infections Protozoan diseases Prot. rettgeri Prot. rettgeri 120 Protriptyline [438-60-8]... [Pg.822]

Desipramine [50-47-5] (35) and nortriptyline [72-69-5] (36) are demethylated derivatives and principal metaboHtes of (32) and (33), respectively. Both compounds possess less sedative and stronger psychomotor effects than the tertiary amine counterparts, probably because tricycHcs containing secondary amine groups generally show greater selectivity for inhibiting the reuptake of norepinephrine compared with the reuptake of serotonin. Protriptyline [438-60-8] (37), a stmctural isomer of nortriptyline, is another important secondary amine that displays a similar clinical profile. [Pg.467]

Dibenzo[a,dlcyclohepta-1,4-diene-5-one Amitriptylin oxide Dibenzo[a,el cycloheptatrien-5-one Cyproheptadine 5H-Dibenzo (a,d 1 cycloheptene Protriptyline... [Pg.1626]

Fluoro uracil mercury Tegafur Formaldehyde Biperiden Bronopol Cortivazol Edetate disodium Glaziovine Hexetidine Meptazinol Metampicillin sodium Methylol riboflavin Nifurfoline Nifurtoinol Noxytiolin Oxymetazoline HCI Phenindamine tartrate Pipebuzone Thihexinol Timonacic sodium Triclobisonium chloride T romethamine Tyloxapol Formamide Cimetide Primidone Protriptyline Razo xane Spiperone Formic acid Bupivacaine... [Pg.1635]

Visumicina Bekanamycin sulfate Visumidriatic - Tropicamide Visutensil Guanethidine sulfate Vitabiotic Methacycline Vitae Chlorpheniramine maleate Vitacarotene - /3-Carotene Vitacid-A Tretinoin Vitacontact Chlorhexidine Vitacort Prednisolone Vitafol Folic acid Vita-K Phytonadione Vitaklorin- Chloramphenicol Vitamin-A-Saure Tretinoin Vitamine K1 Phytonadione Vitarubin Cyanocobalamin Vi-Twel Cyanocobaiamin Vivactil Protriptyline Vival - Diazepam Vivalan Viloxazine HCI... [Pg.1755]

TCAs Once-a-day dosing may be prescribed for maintenance therapy. When the nurse administers the total daily dosage at night, the sedative effects promote sleep, and the adverse reactions appear less troublesome Because protriptyline may produce a mild stimulation in some patients, it is usually not given as a single bedtime dose... [Pg.290]

CH3NO 75-12-7) see Allopurinol Chlorothiazide Cimetidine Fludarabinc phosphate Fluspirilene Heptaminol Primidone Protriptyline Pyridoxine Razoxane Sulfadoxine Theophylline... [Pg.2389]

C24H32O5 32420-16-9) see Nomegestrol acetate 4-(formylmethylainina)benzaic acid (Ci,H,NO, 51865-84-0) see Methotrexate 4-(formylmethylamino)benzayl chloride (C,Hj C1N02 70124-64-0) see Methotrexate 3-(JV-formy l-iV-methylamino)-l -propanol (C5H11NO2 1590-48-3) see Protriptyline... [Pg.2390]

JV-forinyl-yV-methylamino)propyl chloride (CjHioClNO 4172-04-7) see Protriptyline... [Pg.2390]

Amitriptyline, imipramine, desipramine (also likely with nortriptyline, doxepin, protriptyline, and trimipramine)... [Pg.533]

The answer is c. (Hardman, p 436.) The tricyclics and second-generation antidepressants act by blocking serotonin or norepinephrine uptake into the presynaptic terminal. Fluoxetine selectively inhibits serotonin uptake with minimal effects on norepinephrine uptake. Protriptyline, maprotiline, desipramine, and amoxapine have greater effect on norepinephrine uptake... [Pg.156]

Amitriptyline appears to be the tricyclic antidepressant (TCA) of choice, but imipramine, doxepin, nortriptyline, and protriptyline have also been used. [Pg.623]

The most effective treatment for cataplexy is the tricyclic antidepressants, fluoxetine, or venlafaxine. Imipramine, protriptyline, clomipramine, fluoxetine, and nortriptyline are effective in about 80% of patients. [Pg.835]

The antidepressant protriptyline (116) causes skin photosensitization in man. Jones and Sharpies irradiated an aqueous solution of the hydrochloride with a medium-pressure mercury lamp for 16 h and separated the products by preparative TLC. First formed was the epoxide (117) which photohydrated to the diol (118). Also isolated was the enol (119) [84], Earlier, Gasparro and Kochevar had shown that only the hydrochloride was photodegraded under nitrogen in water or ethanol. Three products were isolated and all lysed erythrocytes, but the structure of only one was suggested. This was a cyclobutyl dimer as shown by its mass spectrum and its photolysis back to protriptyline by light of 254 nm. Presumably, a [2 + 2] cycloaddition of the olefine bonds had occurred [85]. [Pg.76]

Dimerization chlorpromazine dithranol protriptyline vanillin ethinyloestradiol folic acid frusemide menadione menaquinone-1... [Pg.114]

Ring dealkylation cinchonidine cinchonine pentobarbitone quinalbarbitone oxytetracycline protriptyline psoralens riboflavin... [Pg.115]

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