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Volumn 15, Issue 2, 2010, Pages 660-671

Antileishmanial, antimicrobial and antifungal activities of some new aryl azomethines

Author keywords

Antibacterial activity; Antifungal activity; Antileishmanial activity; Azomethines; Hetaryl carboxyladehyes; Primary aromatic amines

Indexed keywords

ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTIPARASITIC AGENT; AZO COMPOUND; AZOMETHINE; THIOSEMICARBAZONE DERIVATIVE;

EID: 77649230502     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15020660     Document Type: Article
Times cited : (47)

References (44)
  • 1
    • 0012172271 scopus 로고
    • Tropical disease research progress leishmaniasis
    • World Health Organization: Geneva, Switzerland
    • Modabber, F. Tropical Disease Research Progress Leishmaniasis. In Tropical Disease Research Progress 1991-1992; World Health Organization: Geneva, Switzerland, 1993; pp. 77-87.
    • (1991) Tropical Disease Research Progress , vol.1993 , pp. 77-87
    • Modabber, F.1
  • 2
    • 0030883946 scopus 로고    scopus 로고
    • The current status of antiparasite chemotherapy
    • Croft, S.L. The current status of antiparasite chemotherapy. Parasitology 1997, 114, 3-15.
    • (1997) Parasitology , vol.114 , pp. 3-15
    • Croft, S.L.1
  • 4
    • 11344279997 scopus 로고    scopus 로고
    • Treatment of visceral leishmaniasis in 2004
    • Murray, H.W. Treatment of visceral leishmaniasis in 2004. Am. J. Trop. Med. Hyg. 2004, 71, 787-794.
    • (2004) Am. J. Trop. Med. Hyg. , vol.71 , pp. 787-794
    • Murray, H.W.1
  • 5
    • 0023734112 scopus 로고
    • Recent developments in the chemotherapy of leishmaniasis
    • Croft, S.L. Recent developments in the chemotherapy of leishmaniasis. Trends Pharmacol. Sci. 1988, 9, 376-381.
    • (1988) Trends Pharmacol. Sci. , vol.9 , pp. 376-381
    • Croft, S.L.1
  • 6
    • 0024004690 scopus 로고
    • Chemotherapy for leishmaniasis: Biochemical mechanisms, clinical efficacy, and future strategies
    • Berman, J.D. Chemotherapy for leishmaniasis: biochemical mechanisms, clinical efficacy, and future strategies. Rev. Infect. Dis. 1988, 10, 560-586.
    • (1988) Rev. Infect. Dis. , vol.10 , pp. 560-586
    • Berman, J.D.1
  • 7
    • 0006959950 scopus 로고    scopus 로고
    • Synthesis of transition metal isocyanide complexes containing hydrogen bonding sites in peripheral locations
    • Lau, K.Y.; Mayr, A.; Cheung, K.K. Synthesis of transition metal isocyanide complexes containing hydrogen bonding sites in peripheral locations. Inorg. Chim. Acta. 1999, 285, 223-232.
    • (1999) Inorg. Chim. Acta. , vol.285 , pp. 223-232
    • Lau, K.Y.1    Mayr, A.2    Cheung, K.K.3
  • 8
    • 58349107244 scopus 로고    scopus 로고
    • Synthesis, characterization, antimicrobial and genotoxic activities of new Schiff bases and their complexes
    • Ispir, E.; Toroglu, S.; karyaldiz, A. Synthesis, characterization, antimicrobial and genotoxic activities of new Schiff bases and their complexes. Transition Met. Chem. 2008, 33, 953-960.
    • (2008) Transition Met. Chem. , vol.33 , pp. 953-960
    • Ispir, E.1    Toroglu, S.2    Karyaldiz, A.3
  • 10
    • 0029788683 scopus 로고    scopus 로고
    • Carbonic anhydrase activators. Part 14. Syntheses of mono and bis pyridinium salt derivatives of 2-amino- 5-(2-aminoethyl)- and 2-amino-5-(3-aminopropyl)-1,3,4-Thiadiazole and their interaction with isozyme II
    • Supuran, C.T.; Barboiu, M.; Luca, C.; Pop, E.; Brewster, M.E.; Dinculescu, A. Carbonic anhydrase activators. Part 14. Syntheses of mono and bis pyridinium salt derivatives of 2-amino- 5-(2-aminoethyl)- and 2-amino-5-(3-aminopropyl)-1,3,4-Thiadiazole and their interaction with isozyme II. Eur. J. Med. Chem. 1996, 31, 597-606.
    • (1996) Eur. J. Med. Chem. , vol.31 , pp. 597-606
    • Supuran, C.T.1    Barboiu, M.2    Luca, C.3    Pop, E.4    Brewster, M.E.5    Dinculescu, A.6
  • 11
    • 0010918530 scopus 로고    scopus 로고
    • Schiff bases and their derivatives as potential anticancer agents
    • Sharma, K.P.; Jolly, V.S.; Phatak, P. Schiff bases and their derivatives as potential anticancer agents. Ultra Scient. Phys. Sci. 1998, 10, 263-266.
    • (1998) Ultra Scient. Phys. Sci. , vol.10 , pp. 263-266
    • Sharma, K.P.1    Jolly, V.S.2    Phatak, P.3
  • 13
    • 0017049595 scopus 로고
    • Synthesis of pyrimidine Schiff bases as anticancer agents
    • Shingare, M.S.; Ingle, D.B. Synthesis of pyrimidine Schiff bases as anticancer agents. J. Indian Chem. Soc. 1976, 53, 1036-1037.
    • (1976) J. Indian Chem. Soc. , vol.53 , pp. 1036-1037
    • Shingare, M.S.1    Ingle, D.B.2
  • 14
    • 33847699498 scopus 로고
    • Potential anticancer agents, Schiff bases from p-(3- azaspiro[5,5]undec- 3-yl)benzaldehydes
    • Shkawat, D.R.; Sabins, S.S.; Deliwala, C.V. Potential anticancer agents, Schiff bases from p-(3- azaspiro[5,5]undec-3-yl)benzaldehydes. Bull. Haffkine Inst. 1973, 1, 35-39.
    • (1973) Bull. Haffkine Inst. , vol.1 , pp. 35-39
    • Shkawat, D.R.1    Sabins, S.S.2    Deliwala, C.V.3
  • 16
    • 33847720452 scopus 로고    scopus 로고
    • Synthesis of some novel Schiff bases of 2- aminopyrimidine and their antimicrobial activity
    • Bhendkar, A.K.; Vijay, K.; Raut, A.W. Synthesis of some novel Schiff bases of 2- aminopyrimidine and their antimicrobial activity. Acta Ciencia India Chem. 2004, 30, 29-32.
    • (2004) Acta Ciencia India Chem. , vol.30 , pp. 29-32
    • Bhendkar, A.K.1    Vijay, K.2    Raut, A.W.3
  • 17
    • 31544454176 scopus 로고    scopus 로고
    • Synthesis structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine
    • Vaghasiya, Y.K.; Nair, R.S.; Baluja, M.; Chanda, S.S. Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine. J. Serb. Chem. Soc. 2004, 69, 991-998.
    • (2004) J. Serb. Chem. Soc. , vol.69 , pp. 991-998
    • Vaghasiya, Y.K.1    Nair, R.S.2    Baluja, M.3    Chanda, S.S.4
  • 18
    • 33847734142 scopus 로고    scopus 로고
    • Synthesis of novel Schiff base and azetidinone derivatives and their antibacterial activity
    • Vashi, K.; Naik, H.B. Synthesis of novel Schiff base and azetidinone derivatives and their antibacterial activity. Eur. J. Chem. 2004, 1, 272-276.
    • (2004) Eur. J. Chem. , vol.1 , pp. 272-276
    • Vashi, K.1    Naik, H.B.2
  • 19
    • 0029083716 scopus 로고
    • Therapeutic Potentiation of the immune system by costimulatory Schiff base-forming drugs
    • Rhodes, R.C.; Hall, H.; Beesley, S.R.; Jenkins, J.G.; Collins, D.C.; Zheng, P. Therapeutic Potentiation of the immune system by costimulatory Schiff base-forming drugs. Nature 1995, 377, 71-75.
    • (1995) Nature , vol.377 , pp. 71-75
    • Rhodes, R.C.1    Hall, H.2    Beesley, S.R.3    Jenkins, J.G.4    Collins, D.C.5    Zheng, P.6
  • 20
    • 33847764429 scopus 로고
    • Synthesis anti-tumor and antimicrobial activities of 3-chloro-9- (p-N-substituted sulfamoylphenylaminoethylene) acridines.
    • Safwat, H.M.; Ragab, F.A.; Eid, N.M.; Abdel, G.M. Synthesis, anti-tumor and antimicrobial activities of 3-chloro-9- (p-N-substituted sulfamoylphenylaminoethylene) acridines. Egyptian J. Pharm. Sci. 1988, 29, 99-110.
    • (1988) Egyptian J. Pharm. Sci. , vol.29 , pp. 99-110
    • Safwat, H.M.1    Ragab, F.A.2    Eid, N.M.3    Abdel, G.M.4
  • 21
    • 33847751253 scopus 로고    scopus 로고
    • Synthesis of biologically active p-bis(amino-5-mercapto-1,2,4- triazol-3-yl)benzene and its Schiff base: a new class of bis-triazole
    • Mtrei, R.; Yadawe, M.; Patil, S.A. Synthesis of biologically active p-bis(amino-5-mercapto-1,2,4- triazol-3-yl)benzene and its Schiff base: a new class of bis-triazole. Orient. J. Chem. 1996, 12, 101-102.
    • (1996) Orient. J. Chem. , vol.12 , pp. 101-102
    • Mtrei, R.1    Yadawe, M.2    Patil, S.A.3
  • 22
    • 0000561873 scopus 로고    scopus 로고
    • The preparation, characterization, crystal structure and biological activities of some Cu(II) complexes of the 2-benzoyl pyridine Schiff bases of S-methyl-and S-benzyldithiocarbazate
    • Hossain, M.E.; Allam, M.N.; Begum, J.; Akbar, M.A.; Uddin, M.N.; Smith, F.E.; Hynes, R.C. The preparation, characterization, crystal structure and biological activities of some Cu(II) complexes of the 2-benzoyl pyridine Schiff bases of S-methyl-and S-benzyldithiocarbazate. Inorg. Chim. Acta. 1996, 249, 207-213.
    • (1996) Inorg. Chim. Acta. , vol.249 , pp. 207-213
    • Hossain, M.E.1    Allam, M.N.2    Begum, J.3    Akbar, M.A.4    Uddin, M.N.5    Smith, F.E.6    Hynes, R.C.7
  • 23
    • 0036324391 scopus 로고    scopus 로고
    • Analgesic activity of isatin derivatives
    • Khan, S.A.; Siddiqui, A.A.; Shibeer, B. Analgesic activity of isatin derivatives. Asian J. Chem. 2002, 14, 1117-1118.
    • (2002) Asian J. Chem. , vol.14 , pp. 1117-1118
    • Khan, S.A.1    Siddiqui, A.A.2    Shibeer, B.3
  • 24
    • 1942488330 scopus 로고    scopus 로고
    • Anticonvulsant activity of Schiff bases of isatin derivatives
    • Verma, M.; Pandeya, S.N.; Singh, K.N.; Stables, J.P. Anticonvulsant activity of Schiff bases of isatin derivatives. Acta Pharm. 2004, 54, 49-56.
    • (2004) Acta Pharm. , vol.54 , pp. 49-56
    • Verma, M.1    Pandeya, S.N.2    Singh, K.N.3    Stables, J.P.4
  • 25
    • 4544352331 scopus 로고    scopus 로고
    • Antibacterial Activities of some Amino acid-Schiff bases
    • Sari, N.; Arslan, S.; Logoglu, E.; Sakiyan, L. Antibacterial Activities of some Amino acid-Schiff bases. GUJ Sci. 2003, 16, 283-288.
    • (2003) GUJ Sci. , vol.16 , pp. 283-288
    • Sari, N.1    Arslan, S.2    Logoglu, E.3    Sakiyan, L.4
  • 27
    • 30344484827 scopus 로고    scopus 로고
    • Synthesis and fungicidal activity of new imidazoles from 2-(chloromethyl)-1 H -benzimidazole
    • Madkour, H.; Farag, A.; Ramses, S.; Ibrahiem, N. Synthesis and fungicidal activity of new imidazoles from 2-(chloromethyl)-1 H -benzimidazole. Phosphor. Sulfur Phosphorous Silicon 2006, 181, 255-265.
    • (2006) Phosphor. Sulfur Phosphorous Silicon , vol.181 , pp. 255-265
    • Madkour, H.1    Farag, A.2    Ramses, S.3    Ibrahiem, N.4
  • 28
  • 29
    • 33748282145 scopus 로고    scopus 로고
    • Synthesis and chemoprophylactic effect of novel coumarin derivatives
    • Nofal, Z.M.; El-Zahar, M.I.; Salem, M.A.I.; Madkour, H.M.F. Synthesis and chemoprophylactic effect of novel coumarin derivatives. Egypt J. Chem. 2005, 48, 587-604.
    • (2005) Egypt J. Chem. , vol.48 , pp. 587-604
    • Nofal, Z.M.1    El-Zahar, M.I.2    Salem, M.A.I.3    Madkour, H.M.F.4
  • 30
    • 0035970504 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of new 4H-pyrano [3,2-h]quinolines and fused derivatives
    • Madkour, H.M.F.; Mahmoud, M.R.; Sakr, A.M.; Habashy, M.M. Synthesis and antibacterial activity of new 4H-pyrano [3,2-h]quinolines and fused derivatives. Sci. Pharm. 2001, 69, 33-52.
    • (2001) Sci. Pharm. , vol.69 , pp. 33-52
    • Madkour, H.M.F.1    Mahmoud, M.R.2    Sakr, A.M.3    Habashy, M.M.4
  • 31
    • 0035541917 scopus 로고    scopus 로고
    • A facile one-pot synthesis and antibacterial activity of aziridines and thiazines from 1,3-diarylprop-2-enones
    • Madkour, H.M.F.; Salem, M.A.I.; Soliman, E.A.; Mahmoud, N.F.H. A facile one-pot synthesis and antibacterial activity of aziridines and thiazines from 1,3-diarylprop-2-enones. Phosphor. Sulfur Phosphorous Silicon 2001, 170, 15-28.
    • (2001) Phosphor. Sulfur Phosphorous Silicon , vol.170 , pp. 15-28
    • Madkour, H.M.F.1    Salem, M.A.I.2    Soliman, E.A.3    Mahmoud, N.F.H.4
  • 32
    • 0034193695 scopus 로고    scopus 로고
    • Synthesis of bactericides via carbon nucleophilic addition on 1,3-diarylprop-2-enones as michael acceptors
    • Salem, M.A.I.; Madkour, H.M.F.; Soliman, E.A.; Mahmoud, N.F.H. Synthesis of bactericides via carbon nucleophilic addition on 1,3-diarylprop-2-enones as michael acceptors. Heterocycles 2000, 53, 1129-1143.
    • (2000) Heterocycles , vol.53 , pp. 1129-1143
    • Salem, M.A.I.1    Madkour, H.M.F.2    Soliman, E.A.3    Mahmoud, N.F.H.4
  • 33
    • 0029783353 scopus 로고    scopus 로고
    • Reactions of 3-3-chlorophenyl-1-4-(3,4- methylenedioxybenzylidene) aminophenylprop-2-enone with some nucleophiles
    • Mahmoud, M.R.; Madkour, H.M.F. Reactions of 3-3-chlorophenyl-1-4-(3,4- methylenedioxybenzylidene)aminophenylprop-2-enone with some nucleophiles. Synth. Commun. 1996, 26, 3799-3808.
    • (1996) Synth. Commun. , vol.26 , pp. 3799-3808
    • Mahmoud, M.R.1    Madkour, H.M.F.2
  • 34
    • 33747856086 scopus 로고    scopus 로고
    • Kinetics and mechanism of the Pudovik reaction in the azomethine series: III. Acid-catalyzed hydrophosphorylation of imines
    • Sobanov, A.A.; Zolotukhin, A.V.; Galkina, I.V.; Galkin, V.I.; Cherkasov, R.A. Kinetics and mechanism of the Pudovik reaction in the azomethine series: III. Acid-catalyzed hydrophosphorylation of imines. Russ. J. Gen. Chem. 2006, 76, 421-429.
    • (2006) Russ. J. Gen. Chem. , vol.76 , pp. 421-429
    • Sobanov, A.A.1    Zolotukhin, A.V.2    Galkina, I.V.3    Galkin, V.I.4    Cherkasov, R.A.5
  • 35
    • 33645768328 scopus 로고    scopus 로고
    • Substituent cross-interaction effects on the electronic character of the C=N bridging group in substituted benzylidene anilines - Models for molecular cores of mesogenic compounds. A 13C-NMR study and comparison with theoretical results
    • Neuvonen, H.; Neuvonen, K.; Fülöp, F. Substituent cross-interaction effects on the electronic character of the C=N bridging group in substituted benzylidene anilines - Models for molecular cores of mesogenic compounds. A 13C-NMR study and comparison with theoretical results. J. Org. Chem. 2006, 71, 3141-3148.
    • (2006) J. Org. Chem. , vol.71 , pp. 3141-3148
    • Neuvonen, H.1    Neuvonen, K.2    Fülöp, F.3
  • 36
    • 0041669297 scopus 로고    scopus 로고
    • Molecular structure of di-aryl-aldimines by multinuclear magnetic resonance and X-ray diffraction
    • Montalvo-González, R.; Ariza-Castolo, A.; Molecular structure of di-aryl-aldimines by multinuclear magnetic resonance and X-ray diffraction. J. Mol. Struct. 2003, 655, 375-389.
    • (2003) J. Mol. Struct. , vol.655 , pp. 375-389
    • Montalvo-González, R.1    Ariza-Castolo, A.2
  • 37
    • 77649197844 scopus 로고    scopus 로고
    • Synthesis of some 2-(R, R')-3-(p-nitro phenyl)-thiazolidinone as potent antifungal agents
    • Subudhi, B.B.; Satpathy, S.; Bhatta, D.; Pradhan, D. Synthesis of some 2-(R, R')-3-(p-nitro phenyl)-thiazolidinone as potent antifungal agents. J. Teach. Res. Chem. 2005, 12, 42-45.
    • (2005) J. Teach. Res. Chem. , vol.12 , pp. 42-45
    • Subudhi, B.B.1    Satpathy, S.2    Bhatta, D.3    Pradhan, D.4
  • 38
    • 0012407318 scopus 로고
    • Cycloaddition reactions of meso-ionic oxazolone with cinnamaldehyde anils
    • Sain, B.; Thyagarajan, G.; Sandhu, J.S. Cycloaddition reactions of meso-ionic oxazolone with cinnamaldehyde anils. Can. J. Chem. 1980, 58, 2034-2037.
    • (1980) Can. J. Chem. , vol.58 , pp. 2034-2037
    • Sain, B.1    Thyagarajan, G.2    Sandhu, J.S.3
  • 39
    • 49149085008 scopus 로고
    • Synthesis of antimicrobial heteroaryl-substituted-1,2,3-triazolines via the reaction of diazomethane with anils and mixed azines of thiophenealdehyde and/or isatin
    • Youssef, M.S.K. Synthesis of antimicrobial heteroaryl-substituted-1,2,3- triazolines via the reaction of diazomethane with anils and mixed azines of thiophenealdehyde and/or isatin. J. Chem. Technol. Biotechnol. 1981, 31, 363-367.
    • (1981) J. Chem. Technol. Biotechnol. , vol.31 , pp. 363-367
    • Youssef, M.S.K.1
  • 41
    • 0029395050 scopus 로고
    • Atta-Ur-Rahman. Antifungal steroidal lactones from Withania coagulance
    • Choudhary, M.I.; Dur-e-Shahwar Parveen, Z.; Jabbar, A.; Ali, I.; Atta-Ur-Rahman. Antifungal steroidal lactones from Withania coagulance. Phytochemistry 1995, 40, 1243-1246.
    • (1995) Phytochemistry , vol.40 , pp. 1243-1246
    • Choudhary, M.I.1    Dur-e-Shahwar Parveen, Z.2    Jabbar, A.3    Ali, I.4
  • 42
    • 68949168376 scopus 로고    scopus 로고
    • Antifungal activities of aglaia roxburghiana (W & A)
    • Janaki, S.; Vijayasekaram, V. Antifungal activities of aglaia roxburghiana (W & A). Biomedicine. 1998, 18, 86-89.
    • (1998) Biomedicine , vol.18 , pp. 86-89
    • Janaki, S.1    Vijayasekaram, V.2
  • 44
    • 0347724110 scopus 로고    scopus 로고
    • In vitro antimicrobial activity of propolis and synergism between propolis and antimicrobial drugs
    • Stepanovic, S.; Antic, N.; Dakic, I.; Švabic-Vlahovic, M. In vitro antimicrobial activity of propolis and synergism between propolis and antimicrobial drugs. Microbiol. Res. 2003, 158, 353-357.
    • (2003) Microbiol. Res. , vol.158 , pp. 353-357
    • Stepanovic, S.1    Antic, N.2    Dakic, I.3    Švabic-Vlahovic, M.4


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