2005
DOI: 10.1007/s11172-005-0247-y
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Synthesis of new derivatives of 5,6,7,8-tetrahydro-1,6-naphthyridines and their pharmacological properties

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Cited by 11 publications
(4 citation statements)
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“…2,3 These pyridine structures are the most significant because of their wide spectrum of promising biological activities such as anticonvulsants, 4 anti-inflammatory, 5 antimitotic, 6 agents antioxidant, 7,8 anticancer, 9,10 and antimicrobial activities. 11 Similarly, 1,6-naphthyridines [12][13][14][15][16][17] have established significant attention due to their broad range of bioactivities [18][19][20][21][22][23][24] such as antimicrobial, 25 anti-analgesic, 26 antifungal, 27,28 anticancer, [29][30][31] antioxidant, 31 anti-inflammatory, [27][28][29]32 antiarrhythmic, 33 antitumor 34 , anti HSV-1 35 anti-HIV 36,37 activities and act as inhibitors of acetylcholinesteras. 38 Structures of few previously reported biologically active 1,6-naphyridines (A-G) are shown in Figure 1.…”
Section: Introductionmentioning
confidence: 99%
“…2,3 These pyridine structures are the most significant because of their wide spectrum of promising biological activities such as anticonvulsants, 4 anti-inflammatory, 5 antimitotic, 6 agents antioxidant, 7,8 anticancer, 9,10 and antimicrobial activities. 11 Similarly, 1,6-naphthyridines [12][13][14][15][16][17] have established significant attention due to their broad range of bioactivities [18][19][20][21][22][23][24] such as antimicrobial, 25 anti-analgesic, 26 antifungal, 27,28 anticancer, [29][30][31] antioxidant, 31 anti-inflammatory, [27][28][29]32 antiarrhythmic, 33 antitumor 34 , anti HSV-1 35 anti-HIV 36,37 activities and act as inhibitors of acetylcholinesteras. 38 Structures of few previously reported biologically active 1,6-naphyridines (A-G) are shown in Figure 1.…”
Section: Introductionmentioning
confidence: 99%
“…The Michael addition reaction is one of the most facile and rapid methods for the synthesis 1,5‐dicarbonyl derivatives . These dicarbonyl derivatives can be used as convenient building blocks for constructing dyhydropyridine and pyridine systems , which have been shown to display various biological activities . Presently, we have studied reactions between N ‐substituted piperidine‐4‐ones ( 1 and 2 ) and series of chalcones ( 4–7 ) prepared following previously described literature method under the conditions of Michael addition.…”
Section: Discussionmentioning
confidence: 99%
“…Several anilinoquinolines were established as synthetic antimalarials and have been utilized as synthons in deriving various fused heterocycles such as dibenzonaphthyridines and indoloquinoline alkaloids . Research on naphthyridine chemistry has been expanded considerably in recent years in connection with the fact that these heterocycles exceptionally own a broad spectrum of their biological activities such as anti‐arrhythmic , anti‐analgesic , therapy of disease of human including AIDS , and cancer . Particularly, some dibenzonaphthyridines, that is, quinoline dimers, act as selective 3‐phosphoinositide‐dependent kinase‐I inhibitors .…”
Section: Introductionmentioning
confidence: 99%