1997
DOI: 10.1007/bf02464277
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Structure and antiinflammatory activity of isonicotinic and nicotinic amides

Abstract: It was suggested that butadion and indomethacin, the derivatives of anthranilic acid, are capable of competitively interacting with receptors or enzymatic systems involved in the synthesis, deposition, or release of histamine and serotonin from their depots in tissues. This conclusion was based on the fact that the distance between the carboxy or enolic group and the second reaction center (hydroxy or amino group) in molecules of these antiinflammatory drugs (having an acid character) falls within 0.455-0.480 … Show more

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Cited by 3 publications
(3 citation statements)
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“…Anti-viral medication Amizon (Amizonum Ò , Farmak Ltd, Ukraine) served as a positive control. Amizon or l-methyl-4-(benzylaminocarbonyl) pyridinium iodide [4], CAS Registry Number: 201349-37-3 is a low toxicity compound with well established anti-viral properties [22] that has been used for influenza prophylaxis and treatment. Tamiflu (F. Hoffmann-La Roshe Ltd., Switzerland) and Rimantadine (OlainFarm, Latvia) were used in study of orthomyxoviruses only.…”
Section: Methodsmentioning
confidence: 99%
“…Anti-viral medication Amizon (Amizonum Ò , Farmak Ltd, Ukraine) served as a positive control. Amizon or l-methyl-4-(benzylaminocarbonyl) pyridinium iodide [4], CAS Registry Number: 201349-37-3 is a low toxicity compound with well established anti-viral properties [22] that has been used for influenza prophylaxis and treatment. Tamiflu (F. Hoffmann-La Roshe Ltd., Switzerland) and Rimantadine (OlainFarm, Latvia) were used in study of orthomyxoviruses only.…”
Section: Methodsmentioning
confidence: 99%
“…The title compound can be synthesized from N-benzylamide 4-pyridinecarboxylic acid C 5 H 4 NCONHCH 2 C 6 H 5 and methyl iodide MeI in a 1:2 (Trinus et al, 1994) or 1:1.2 (Buhtiarova et al, 1997) molar ratio. N-Benzylamide 4-pyridinecarboxylic acid, in turn, was synthesized by the condensation of isonicotinic acid C 5 H 4 NCOOH with benzylamine C 6 H 5 CH 2 NH 2 taken in a 1:2 molar ratio (Trinus et al, 1994).…”
Section: Synthesis and Crystallizationmentioning
confidence: 99%
“…Amides bearing a trifluoromethyl substituent show a broad spectrum of pharmacological properties, including antitumour [1], anti-inflammatory [2], antioxidant [3], analgesic [4] and antiviral activity [5]. It was also reported that substituted amides show higher anticonvulsive [6], hypoglycemic [7], antiarrhythmic [8] and fungicidal activity [9].…”
mentioning
confidence: 99%