[TREATMENT OF HYMENOLEPIASIS NANA WITH A SALICYLAMIDE DERIVATIVE (N-(2'-CHLORO-4'-NITROPHENYL)-5-CHLOROSALICYLAMIDE)].
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Cestode Infections↗
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Results for “SALICYLAMIDE”
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[TREATMENT OF HYMENOLEPIASIS WITH A SALICYLAMIDE DERIVATIVE].
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Cestode Infections↗
[Studies on the metabolism of salicylamide and its therapeutic use].
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Salicylamides↗
[Self-treatment with salicylamide (R 12)].
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Salicylamides↗
[Therapeutic revaluation of orthooxybenzoic amide (salicylamide)].
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Amides↗
Salicylamide; pharmacology, fate and clinical use.
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Salicylamides↗
Absorption and distribution of salicylamide.
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Animals↗
[Salicylamide in antirheumatic therapy].
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Antirheumatic Agents↗
[Absorption and excretion of salicylamide following oral and percutaneous administration].
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Administration, Cutaneous↗
Antipyretic activity of acetylsalicylic acid and salicylamide suspension in pediatrics. A comparative clinical evaluation in two hundred six cases.
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Antipyretics↗
Effectiveness of salicylamide as an analgesic and antirheumatic agent; evaluation of the double blindfold technique for studying analgesic drugs.
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Analgesics↗
Salicylamide and acetylsalicylic acid in recurrent urolithiasis.
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Aspirin↗
Antipyretic effectiveness of salicylamide and acetylsalicyclic acid in infants; a comparative study.
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Antipyretics↗
[Determination of salicylamide in blood using direct injection HPLC].
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Chromatography, High Pressure Liquid↗
Synthesis of some N-substituted salicylamides structurally related to certain antimicrobials.
The condensation of 5-nitrosalicoylchloride and 5-sulphamoylsalicylic acid with certain amines is described. Reacting the acid chloride with 3-amino-2-oxazolidone, 4-aminophenazone, thiosemicarbazide, 1-aminohydantoin and 2-aminopyridine yielded the correspondong N-substituted 5-nitrosalicylamides (1a-c), while with semicarbazide a disubstituted product type 2 was obtained. On the other hand, when 5-sulphamoylsalicylic acid was condensed with o-chloroaniline, m-chloroaniline and 4-aminophenazone in the presence of phosphorus trichloride, instead of affording the expected condensation products type 3, it yielded N1N5-disubstituted 5-sulphamoylsalicylamides (4a-c). The synthesized compounds were screened for antimicrobial activity.
Antifungal Agents↗
[Synthesis of N-amidinobenzyl derivatives of salicylamide, 2,4-dioxodihydro-5,6-benzoxazine-(1,3) and -benzothiazine-(1,3) and of 2,4-dioxo-1,2,3,4-tetrahydroquinazoline].
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Alkylation↗
Salicylamide metabolism in acute intermittent porphyria.
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Acute Disease↗