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Volumn 78, Issue 3, 2011, Pages 464-470

Design, Synthesis, and Evaluation of Thiazolidinone Derivatives as Antimicrobial and Anti-viral Agents

Author keywords

Anti viral; Antibacterial; Antifungal; Schiff's reaction; Thiazolidinones

Indexed keywords

2 (2 CHLOROPHENYL) 3 (4 SULPHONAMIDOPHENYL)THIAZOLIDIN 4 ONE; 2 (2,5 DIMETHOXYPHENYL) 3 (PYRIDIN 2 YL)THIAZOLIDIN 4 ONE; 2 (2,5 DIMETHOXYPHENYL) 3 PHENETHYLTHIAZOLIDIN 4 ONE; 2 (2,6 DICHLOROPHENYL) 3 (4,6 DIMETHYLPYRIDIN 2 YL)THIAZOLIDIN 4 ONE; 2 (2,6 DICHLOROPHENYL) 3 PHENETHYLTHIAZOLIDIN 4 ONE; 2 (2,6 DIMETHOXYPHENYL) 3 (6 METHYLPYRIDIN 2 YL)THIAZOLIDIN 4 ONE; 2 (4 METHOXYPHENYL) 3 (4 SULPHONAMIDOPHENYL)THIAZOLIDIN 4 ONE; 3 (4 CHLOROPHENYL) 2 (4 NITROPHENYL)THIAZOLIDIN 4 ONE; 3 (5 CHLOROPYRIDIN 2 YL) 2 (PYRIDINE 2 YL)THIAZOLIDIN 4 ONE; 3 (6 METHYLPYRIDIN 2 YL) 2 (PYRIDINE 2 YL)THIAZOLIDIN 4 ONE; ALDEHYDE; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTIVIRUS AGENT; AROMATIC AMINE; BENZENE; CIPROFLOXACIN; FLUCONAZOLE; GANCICLOVIR; NEVIRAPINE; RIBAVIRIN; THIAZOLIDIN 4 ONE DERIVATIVE; THIOGLYCOLIC ACID; TOLUENE; UNCLASSIFIED DRUG; ZIDOVUDINE;

EID: 80051590689     PISSN: 17470277     EISSN: 17470285     Source Type: Journal    
DOI: 10.1111/j.1747-0285.2011.01149.x     Document Type: Article
Times cited : (42)

References (18)
  • 2
    • 0041831030 scopus 로고    scopus 로고
    • Novel inhibitors of an emerging target in Mycobacterium tuberculosis, substituted thiazolidinones as inhibitors of dTDP-rhamnose synthesis
    • Babaoglu K., Page M.A., Jones V.C., McNeil M.R., Dong C., Naismith J.H., Lee R.E. (2003) Novel inhibitors of an emerging target in Mycobacterium tuberculosis, substituted thiazolidinones as inhibitors of dTDP-rhamnose synthesis. Bioorg Med Chem Lett;13:3227-3230.
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 3227-3230
    • Babaoglu, K.1    Page, M.A.2    Jones, V.C.3    McNeil, M.R.4    Dong, C.5    Naismith, J.H.6    Lee, R.E.7
  • 3
    • 0023779475 scopus 로고
    • Compounds with potential antitumor activity. VI--2-Alkyl-3-[2-(1,3,4-thiadiazolyl)]-4-thiazolidinones
    • Grasso S., Chimirri A., Monforte P., Fenech G., Zappala M., Monforte A.M. (1988) Compounds with potential antitumor activity. VI--2-Alkyl-3-[2-(1, 3, 4-thiadiazolyl)]-4-thiazolidinones. Farmaco;43:851-856.
    • (1988) Farmaco , vol.43 , pp. 851-856
    • Grasso, S.1    Chimirri, A.2    Monforte, P.3    Fenech, G.4    Zappala, M.5    Monforte, A.M.6
  • 6
    • 0025915144 scopus 로고
    • Synthesis, anticonvulsant properties of 3-(1,3,4-thiadiazol-2-yl)thiazolidin-4-ones
    • Chimirri A., Grasso S., Monforte A.M., Zappala M., De Sarro A., De Sarro G.B. (1991) Synthesis, anticonvulsant properties of 3-(1, 3, 4-thiadiazol-2-yl)thiazolidin-4-ones. Farmaco;46:935-943.
    • (1991) Farmaco , vol.46 , pp. 935-943
    • Chimirri, A.1    Grasso, S.2    Monforte, A.M.3    Zappala, M.4    De Sarro, A.5    De Sarro, G.B.6
  • 9
    • 0025812546 scopus 로고
    • Anti-HIV agents Synthesis II., in vitro anti-HIV activity of novel 1H,3H-thiazolo[3,4-a]benzimidazoles
    • Chimirri A., Grasso S., Monforte A.M., Zappala M. (1991) Anti-HIV agents Synthesis II., in vitro anti-HIV activity of novel 1H, 3H-thiazolo[3, 4-a]benzimidazoles. Farmaco;46:925-933.
    • (1991) Farmaco , vol.46 , pp. 925-933
    • Chimirri, A.1    Grasso, S.2    Monforte, A.M.3    Zappala, M.4
  • 13
    • 33847781693 scopus 로고    scopus 로고
    • Design, synthesis, evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents
    • Rawal R.K., Tripathi R., Katti S.B., Pannecouque C., De Clercq E. (2007) Design, synthesis, evaluation of 2-aryl-3-heteroaryl-1, 3-thiazolidin-4-ones as anti-HIV agents. Bioorg Med Chem;4:1725-1731.
    • (2007) Bioorg Med Chem , vol.4 , pp. 1725-1731
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 14
    • 34250186053 scopus 로고    scopus 로고
    • Synthesis, anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones
    • Balzarini J., Orzeszko B., Maurin J.K., Orzeszko A. (2007) Synthesis, anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones. Eur J Med Chem;42:993-1003.
    • (2007) Eur J Med Chem , vol.42 , pp. 993-1003
    • Balzarini, J.1    Orzeszko, B.2    Maurin, J.K.3    Orzeszko, A.4
  • 15
    • 57949109639 scopus 로고    scopus 로고
    • Synthesis, anti-HIV studies of 2-, 3-adamantyl-substituted thiazolidin-4-ones
    • Balzarini J., Orzeszko B., Maurin J.K., Orzeszko A. (2009) Synthesis, anti-HIV studies of 2-, 3-adamantyl-substituted thiazolidin-4-ones. Eur J Med Chem;44:303-311.
    • (2009) Eur J Med Chem , vol.44 , pp. 303-311
    • Balzarini, J.1    Orzeszko, B.2    Maurin, J.K.3    Orzeszko, A.4
  • 16
    • 0018346786 scopus 로고
    • Reaction of 1-formyladamantane with heterocyclic compounds. Mass spectra, antibacterial, antifungal activity
    • Fenech G., Monforte P., Chimirri A., Grasso S. (1979) Reaction of 1-formyladamantane with heterocyclic compounds. Mass spectra, antibacterial, antifungal activity. J Heterocycl Chem;16:347-351.
    • (1979) J Heterocycl Chem , vol.16 , pp. 347-351
    • Fenech, G.1    Monforte, P.2    Chimirri, A.3    Grasso, S.4
  • 18
    • 60849112247 scopus 로고    scopus 로고
    • Predicting anti-HIV activity of 1,3,4-thiazolidinone derivatives: 3QSAR D approach
    • Ravichandran V., Prashanthakumar B.R., Sankar S., Agrawal R.K. (2009) Predicting anti-HIV activity of 1, 3, 4-thiazolidinone derivatives: 3QSAR D approach. Eur J Med Chem;44:1180-1187.
    • (2009) Eur J Med Chem , vol.44 , pp. 1180-1187
    • Ravichandran, V.1    Prashanthakumar, B.R.2    Sankar, S.3    Agrawal, R.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.