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Volumn 8, Issue 3, 2011, Pages 276-283

Synthesis, characterization of some new five membered heterocycles based on imidazole moiety and their applications on therapeutics

Author keywords

2 (2,4,5 triphenyl 1H imidazol 1 yl)acetohydrazide; Antibacterial activity; Antifungal activity; Antioxidant activity; Five membered heterocycles; Microwave irradiation

Indexed keywords

1 [2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)ACETYL] (1,2 DIHYDRO 5 METHYL)PYRAZOL 3 ONE; 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL) 1 (3,5 DIMETHYL 1H PYRAZOL 1 YL)ETHANONE; 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL) N (2,5 DIMETHYL 1H PYRROL 1 YL)ACETAMIDE; 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)ACETATE; 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)ACETOHYDRAZIDE; 2 (4 CHLOROPHENYL) 5 [(2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)METHYL] 1,3,4 OXADIAZOLE; 2 (4 NITROPHENYL) 5 [(2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)METHYL] 1,3,4 OXADIAZOLE; 2 [(2,4 DICHLOROPHENOXY)METHYL] 5 [(2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)METHYL] 1,3,4 OXADIAZOLE; 2 [(NAPHTHALEN 2 YLOXY)METHYL] 5 [(2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)METHYL] 1,3,4 OXADIAZOLE; 2 PHENYL 5 [(2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)METHYL] 1,3,4 OXADIAZOLE; AMPHOTERICIN B; ANTIFUNGAL AGENT; ANTIOXIDANT; IMIDAZOLE DERIVATIVE; N (1,3 DIOXOISOINDOLIN 2 YL) 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)ACETAMIDE; N (2,5 DIOXO 2,5 DIHYDRO 1H PYRROL 1 YL) 2 (2,4,5 TRIPHENYL 1H IMIDAZOL 1 YL)ACETAMIDE; NITROFURANTOIN; NITROGEN; TETRACYCLINE; UNCLASSIFIED DRUG;

EID: 79952299761     PISSN: 15701808     EISSN: None     Source Type: Journal    
DOI: 10.2174/157018011794578196     Document Type: Article
Times cited : (10)

References (35)
  • 1
    • 0034141601 scopus 로고    scopus 로고
    • Marine natural products
    • (a) Faulkner, D. J. Marine natural products. Nat. Prod. Rep., 2000, 17, 1-55.
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 1-55
    • Faulkner, D.J.1
  • 2
    • 0036005608 scopus 로고    scopus 로고
    • Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids
    • (b) Lewis, J. R. Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids. Nat. Prod. Rep., 2002, 19, 223-258;
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 223-258
    • Lewis, J.R.1
  • 3
    • 0035984558 scopus 로고    scopus 로고
    • Muscarine, imidazole, oxazole, thiazole, Amaryllidaceae and Sceletium alkaloids
    • (c) Jin, Z.; Li, Z.; Huang, R. Muscarine, imidazole, oxazole, thiazole, Amaryllidaceae and Sceletium alkaloids. Nat. Prod. Rep. 2002, 19, 454-476;
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 454-476
    • Jin, Z.1    Li, Z.2    Huang, R.3
  • 5
    • 0016259815 scopus 로고
    • Preparation and antiinflammatory activity of some nonacidic trisubstituted imidazoles
    • (a) Lombardino, J. G.; Wiseman, E. H. Preparation and antiinflammatory activity of some nonacidic trisubstituted imidazoles. J. Med. Chem. 1974, 17, 1182-1188;
    • (1974) J. Med. Chem. , vol.17 , pp. 1182-1188
    • Lombardino, J.G.1    Wiseman, E.H.2
  • 6
    • 33847613840 scopus 로고
    • Pharmaceutical imidazoles
    • Ger. Offen. 2155558, 1972
    • (b) Lombardino, J. G. Pharmaceutical imidazoles. Ger. Offen. 2155558, 1972; Chem. Abstr., 1972, 77, 1016074;
    • (1972) Chem. Abstr. , vol.77 , pp. 1016074
    • Lombardino, J.G.1
  • 7
    • 19544394147 scopus 로고
    • Antithrombotic triphenylimidazoles
    • Eur. Pat. Appl. EP58890, 1982
    • (c) Phillips, A. P.; White, H. L.; Rosen, S. Antithrombotic triphenylimidazoles. Eur. Pat. Appl. EP58890, 1982; Chem. Abstr., 1983, 98, 53894z.
    • (1983) Chem. Abstr. , vol.98
    • Phillips, A.P.1    White, H.L.2    Rosen, S.3
  • 9
    • 19544389917 scopus 로고
    • Preparation of 1-phenyl-2-imidazolidinones and -2-imidazolidinethiones as herbicides
    • Ger. Offen. Pat., 3604042, 1987
    • Liebl, R.; Handte, R.; Mildenberger, H.; Bauer, K.; Bieringer, H. Preparation of 1-phenyl-2-imidazolidinones and -2-imidazolidinethiones as herbicides. Ger. Offen. Pat., 3604042, 1987; Chem. Abstr., 1987, 108, 6018g.
    • (1987) Chem. Abstr. , vol.108
    • Liebl, R.1    Handte, R.2    Mildenberger, H.3    Bauer, K.4    Bieringer, H.5
  • 10
    • 70449648421 scopus 로고
    • Heterocycle-containing amidine derivatives, their preparation, and use as LTB4 antagonists
    • Patent WO 9421616, 1994
    • Renth, E. O.; Schromm, K.; Anderskewitz, R.; Birke, F.; Fuegner, A.; Heuer, H. Heterocycle-containing amidine derivatives, their preparation, and use as LTB4 antagonists. Patent WO 9421616, 1994; Chem. Abstr., 1995, 122, 81416c.
    • (1995) Chem. Abstr. , vol.122
    • Renth, E.O.1    Schromm, K.2    Anderskewitz, R.3    Birke, F.4    Fuegner, A.5    Heuer, H.6
  • 11
    • 70449655820 scopus 로고
    • Preparation and formulation of imidazoles, imidazopyridines, and imidazopyrimidines as inflammation inhibitors
    • U.S. Patent, 4810828, 1989
    • Fenske, D. C.; Kuo, E. A.; Tully, W. R. Preparation and formulation of imidazoles, imidazopyridines, and imidazopyrimidines as inflammation inhibitors. U.S. Patent, 4810828, 1989; Chem. Abstr., 1988, 109, 170425d.
    • (1988) Chem. Abstr. , vol.109
    • Fenske, D.C.1    Kuo, E.A.2    Tully, W.R.3
  • 12
    • 70449689768 scopus 로고
    • Thiomethyl and sulfinylmethyl derivatives having gastric acid antisecretory activity, processes for their preparation, and pharmaceutical compositions containing them
    • EP Patent, 301422, 1989
    • Chiesi, P.; Servadio, V.; Razzetti, R. Thiomethyl and sulfinylmethyl derivatives having gastric acid antisecretory activity, processes for their preparation, and pharmaceutical compositions containing them. EP Patent, 301422, 1989; Chem. Abstr., 1989, 111, 225320q.
    • (1989) Chem. Abstr. , vol.111
    • Chiesi, P.1    Servadio, V.2    Razzetti, R.3
  • 13
    • 70449679977 scopus 로고
    • Preparation of heterocyclic carbostyril derivatives as inhibitors of thrombocyte adhesion
    • EP Patent, 240015, 1987
    • Nishi, T.; Uno, T.; Koga, Y.; Chu, G. N. Preparation of heterocyclic carbostyril derivatives as inhibitors of thrombocyte adhesion. EP Patent, 240015, 1987; Chem. Abstr., 1988, 108, 167318v.
    • (1988) Chem. Abstr. , vol.108
    • Nishi, T.1    Uno, T.2    Koga, Y.3    Chu, G.N.4
  • 14
    • 0342908579 scopus 로고
    • 1-substituted imidazole-5-carboxylic acid derivatives, their preparation and their use as biocides
    • U.S. Patent, 820335, 1989
    • Maier, T.; Schmierer, R.; Bauer, K.; Bieringer, H.; Buerstell, H.; Sachse, B. 1-substituted imidazole-5-carboxylic acid derivatives, their preparation and their use as biocides. U.S. Patent, 820335, 1989; Chem. Abstr., 1989, 111, 19494.
    • (1989) Chem. Abstr. , vol.111 , pp. 19494
    • Maier, T.1    Schmierer, R.2    Bauer, K.3    Bieringer, H.4    Buerstell, H.5    Sachse, B.6
  • 15
    • 0031494993 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of 1,2-disubstituted 4-[(5-substituted 2-phenylindol-3-yl)methylene] imidazolin-5-(4H)-ones
    • Renukadevi, P.; Biradar, J. S.; Hiremath, S. P.; Manjunath, S. Y. Synthesis and antibacterial activity of 1,2-disubstituted 4-[(5-substituted 2-phenylindol-3-yl)methylene] imidazolin-5-(4H)-ones. Indian J. Heterocycl. Chem., 1997, 6, 277-280.
    • (1997) Indian J. Heterocycl. Chem. , vol.6 , pp. 277-280
    • Renukadevi, P.1    Biradar, J.S.2    Hiremath, S.P.3    Manjunath, S.Y.4
  • 16
    • 0038710209 scopus 로고
    • Antisenescence activity of 4,5-disubstituted imidazoles: New cytokinin mimics
    • Patricia, L. C.; Christine, M. G.; Stephen, B. M. Antisenescence activity of 4,5-disubstituted imidazoles: new cytokinin mimics. J. Agric. Food Chem., 1988, 36, 1076-1079.
    • (1988) J. Agric. Food Chem. , vol.36 , pp. 1076-1079
    • Patricia, L.C.1    Christine, M.G.2    Stephen, B.M.3
  • 17
    • 0032544143 scopus 로고    scopus 로고
    • Novel imidazole derivatives with subtype-selective antimuscarinic activity
    • Miyachi, H.; Kiyota, H.; Segawa, M. Novel imidazole derivatives with subtype-selective antimuscarinic activity. Bioorg. Med. Chem. Lett., 1998, 18, 2163-2168.
    • (1998) Bioorg. Med. Chem. Lett. , vol.18 , pp. 2163-2168
    • Miyachi, H.1    Kiyota, H.2    Segawa, M.3
  • 18
    • 0022219890 scopus 로고
    • Preparation, antiarthritic and analgesic activity of 4,5-diaryl-2- (substituted thio)-1H-imidazoles and their sulfoxides and sulfones
    • Sharpe, T. R.; Cherkovsky, S. C.; Hewes, W. E.; Smith, D. H.; Gregory, W. A.; Haber, S. B.; Leadbetter, M. R.; Whitney, J. G. Preparation, antiarthritic and analgesic activity of 4,5-diaryl-2-(substituted thio)-1H-imidazoles and their sulfoxides and sulfones. J. Med. Chem., 1985, 28, 1188-1194.
    • (1985) J. Med. Chem. , vol.28 , pp. 1188-1194
    • Sharpe, T.R.1    Cherkovsky, S.C.2    Hewes, W.E.3    Smith, D.H.4    Gregory, W.A.5    Haber, S.B.6    Leadbetter, M.R.7    Whitney, J.G.8
  • 19
    • 0023212166 scopus 로고
    • Cardiotonic agents. 5. 1,2-Dihydro-5-[4-(1H-imidazol-1-yl)phenyl]-6- methyl-2-oxo-3-pyridinecarbonitriles and related compounds. Synthesis and inotropic activity
    • Sircar, I.; Duell, B. L.; Bristol, A.; Weishaar, R. E.; Evans, D. B. Cardiotonic agents. 5. 1,2-Dihydro-5-[4-(1H-imidazol-1-yl)phenyl]-6-methyl-2- oxo-3-pyridinecarbonitriles and related compounds. Synthesis and inotropic activity. J. Med. Chem., 1987, 30, 1023-1029.
    • (1987) J. Med. Chem. , vol.30 , pp. 1023-1029
    • Sircar, I.1    Duell, B.L.2    Bristol, A.3    Weishaar, R.E.4    Evans, D.B.5
  • 20
    • 0023937044 scopus 로고
    • (Imidazo[1,2-a]pyrimidin-2-yl)phenylmethanones and related compounds as potential nonsedative anxiolytics
    • Jewery, S. C.; Danswan, G.; Gardner, C. R.; Matharu, S. S.; Murdoch, R.; Tully, W. R.; Westwood, R. (Imidazo[1,2-a]pyrimidin-2-yl)phenylmethanones and related compounds as potential nonsedative anxiolytics. J. Med. Chem., 1988, 31, 1220-1226.
    • (1988) J. Med. Chem. , vol.31 , pp. 1220-1226
    • Jewery, S.C.1    Danswan, G.2    Gardner, C.R.3    Matharu, S.S.4    Murdoch, R.5    Tully, W.R.6    Westwood, R.7
  • 21
    • 0027270448 scopus 로고
    • Structure-activity relationship of N-[2-(dimethylamino)-6-[3-(5-methyl-4- phenyl-1H-imidazol-1-yl)propoxy]phenyl]-N′-pentylurea and analogs. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity
    • Kimura, T.; Takase, Y.; Hayashi, K.; Tanaka, H.; Ohtsuka, I.; Saeki, T.; Kogushi, M.; Yamada, T.; Fujimori, T.; Saitou, I.; Akasaka, K. Structure-activity relationship of N-[2-(dimethylamino)-6-[3-(5-methyl-4-phenyl- 1H-imidazol-1-yl)propoxy]phenyl]-N′-pentylurea and analogs. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. J. Med. Chem., 1993, 36, 1630-1640.
    • (1993) J. Med. Chem. , vol.36 , pp. 1630-1640
    • Kimura, T.1    Takase, Y.2    Hayashi, K.3    Tanaka, H.4    Ohtsuka, I.5    Saeki, T.6    Kogushi, M.7    Yamada, T.8    Fujimori, T.9    Saitou, I.10    Akasaka, K.11
  • 22
    • 0027145575 scopus 로고    scopus 로고
    • Inhibitors of cholesterol biosynthesis. 1. 3,5-Dihydroxy-7-(N-imidazolyl) -6-heptenoates and -heptanoates, a novel series of 3-hydroxy-3-methylglutarate- CoA reductase inhibitors
    • Chuen, C.; Bailey, E. J. Inhibitors of cholesterol biosynthesis. 1. 3,5-Dihydroxy-7-(N-imidazolyl)-6-heptenoates and -heptanoates, a novel series of 3-hydroxy-3-methylglutarate-CoA reductase inhibitors. J. Med. Chem., 1996, 36, 3646-3657.
    • (1996) J. Med. Chem. , vol.36 , pp. 3646-3657
    • Chuen, C.1    Bailey, E.J.2
  • 23
    • 0027428755 scopus 로고
    • Imidazol-1-yl and pyridin-3-yl derivatives of 4-phenyl-1,4- dihydropyridines combining Ca2+ antagonism and thromboxane A2 synthase inhibition
    • Cozzi, P.; Carganico, G.; Fusar, D.; Grossoni, M.; Menichincheri, M.; Pinciroli, V.; Tonani, R.; Vaghi, F.; Salvati, P. Imidazol-1-yl and pyridin-3-yl derivatives of 4-phenyl-1,4-dihydropyridines combining Ca2+ antagonism and thromboxane A2 synthase inhibition. J. Med. Chem., 1993, 36, 2964-2972.
    • (1993) J. Med. Chem. , vol.36 , pp. 2964-2972
    • Cozzi, P.1    Carganico, G.2    Fusar, D.3    Grossoni, M.4    Menichincheri, M.5    Pinciroli, V.6    Tonani, R.7    Vaghi, F.8    Salvati, P.9
  • 24
    • 0036661548 scopus 로고    scopus 로고
    • Condensed bridgehead nitrogen heterocyclic systems: Facile synthesis and antimicrobial activity of imidazo[2,1-b]-1,3,4-thiazoles
    • Mohan, J.; Kumar, A. Condensed bridgehead nitrogen heterocyclic systems: Facile synthesis and antimicrobial activity of imidazo[2,1-b]-1,3,4-thiazoles. Indian J. Heterocycl. Chem., 2002, 12, 41-44.
    • (2002) Indian J. Heterocycl. Chem. , vol.12 , pp. 41-44
    • Mohan, J.1    Kumar, A.2
  • 26
    • 0025157632 scopus 로고
    • Synthesis, anticonvulsant and enzyme-inhibitory activities of some indolyl-1,3,4-thiadiazoles
    • Meenakshi, S.; Reenakalsi; Renusah; Dixit, K. S.; Nath, C.; Barthwal, J. P. Synthesis, anticonvulsant and enzyme-inhibitory activities of some indolyl-1,3,4-thiadiazoles. Indian J. Chem., 1990, 29B, 85-87.
    • (1990) Indian J. Chem. , vol.29 B , pp. 85-87
    • Meenakshi, S.1    Reenakalsi2    Renusah3    Dixit, K.S.4    Nath, C.5    Barthwal, J.P.6
  • 27
    • 0017874339 scopus 로고
    • 2-(Alkoxyaryl)-2-imidazoline monoamine oxidase inhibitors with antidepressant activity
    • Harfenist, M.; Soroko, E. F.; Mekenzie, G. M. 2-(Alkoxyaryl)-2- imidazoline monoamine oxidase inhibitors with antidepressant activity. J. Med. Chem. , 1978, 21, 405-409.
    • (1978) J. Med. Chem. , vol.21 , pp. 405-409
    • Harfenist, M.1    Soroko, E.F.2    Mekenzie, G.M.3
  • 28
    • 34447555909 scopus 로고    scopus 로고
    • New heterocyclic mono- and bis-(α-hydroxymethyl) phosphonic acids: Synthesis and Cu (II) binding abilities
    • Olszewski, T. K.; Galezowska, J.; Boduszek, B.; Kozlowski, H. New heterocyclic mono- and bis-(α-hydroxymethyl) phosphonic acids: Synthesis and Cu (II) binding abilities. Eur. J. Org. Chem., 2007, 3539-3546.
    • (2007) Eur. J. Org. Chem. , pp. 3539-3546
    • Olszewski, T.K.1    Galezowska, J.2    Boduszek, B.3    Kozlowski, H.4
  • 29
    • 67650838750 scopus 로고    scopus 로고
    • Surface-enhanced raman scattering studies on the interaction of phosphonate derivatives of imidazole, thiazole, and pyridine with silver electrode in aqueous solution
    • Podstawka, E.; Kudelski, A.; Olszewski, T. K.; Boduszek, B. Surface-enhanced raman scattering studies on the interaction of phosphonate derivatives of imidazole, thiazole, and pyridine with silver electrode in aqueous solution. J. Phys. Chem. B., 2009, 113, 10035-10042.
    • (2009) J. Phys. Chem. B. , vol.113 , pp. 10035-10042
    • Podstawka, E.1    Kudelski, A.2    Olszewski, T.K.3    Boduszek, B.4
  • 30
    • 69549106063 scopus 로고    scopus 로고
    • Adsorbed states of phosphonate derivatives of N-heterocyclic aromatic compounds, imidazole, thiazole, and pyridine on colloidal silver: Comparison with a silver electrode
    • Podstawka, E.; Olszewski, T. K.; Boduszek, B., Proniewicz, L. Adsorbed states of phosphonate derivatives of N-heterocyclic aromatic compounds, imidazole, thiazole, and pyridine on colloidal silver: comparison with a silver electrode. J. Phys. Chem. B., 2009, 113, 12013-12018.
    • (2009) J. Phys. Chem. B. , vol.113 , pp. 12013-12018
    • Podstawka, E.1    Olszewski, T.K.2    Boduszek, B.3    Proniewicz, L.4
  • 31
    • 76149084686 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of new Schiff bases containing coumarin moiety and their spectral characterization
    • Satyanarayana, V. S. V.; Sreevani, P.; Sivakumar, A.; Vijayakumar, V. Synthesis and antimicrobial activity of new Schiff bases containing coumarin moiety and their spectral characterization. ARKIVOC, 2008, xvii, 221-233.
    • (2008) ARKIVOC , vol.17 , pp. 221-233
    • Satyanarayana, V.S.V.1    Sreevani, P.2    Sivakumar, A.3    Vijayakumar, V.4
  • 32
    • 0000200150 scopus 로고
    • An antibiotic assay by the agar well diffusion method
    • Perez, C.; Paul, M.; Bazerque, P. An antibiotic assay by the agar well diffusion method. Acta Biol. Med. Exp., 1990, 15, 113-115.
    • (1990) Acta Biol. Med. Exp. , vol.15 , pp. 113-115
    • Perez, C.1    Paul, M.2    Bazerque, P.3
  • 33
    • 0013902668 scopus 로고
    • Antibiotic susceptibility testing by a standardized single disk method
    • Bauer, A. W.; Kirby, W. M.; Sherris, J. C.; Turck, M. Antibiotic susceptibility testing by a standardized single disk method. Am. J. Clin. Pathol., 1966, 45(4), 493-496.
    • (1966) Am. J. Clin. Pathol. , vol.45 , Issue.4 , pp. 493-496
    • Bauer, A.W.1    Kirby, W.M.2    Sherris, J.C.3    Turck, M.4
  • 35
    • 28944434991 scopus 로고    scopus 로고
    • Synergistic antioxidative effects of alkamides, caffeic acid derivatives, and polysaccharide fractions from Echinacea purpurea on in vitro oxidation of human low-density lipoproteins
    • Dalby-Brown, L.; Basett, H.; Landbo, A. K.; Meyer, A.; Molgaard, P. Synergistic antioxidative effects of alkamides, caffeic acid derivatives, and polysaccharide fractions from Echinacea purpurea on in vitro oxidation of human low-density lipoproteins. J. Agric. Food Chem., 2005, 53, 9413-9423.
    • (2005) J. Agric. Food Chem. , vol.53 , pp. 9413-9423
    • Dalby-Brown, L.1    Basett, H.2    Landbo, A.K.3    Meyer, A.4    Molgaard, P.5


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