메뉴 건너뛰기




Volumn 64, Issue , 2013, Pages 74-80

Synthesis, antifungal and cytotoxic activities of 2-aryl-3-((piperidin-1- yl)ethyl)thiazolidinones

Author keywords

Antifungal activity; Cytotoxicity; One pot reaction; Rhodotorula sp; Thiazolidinones

Indexed keywords

2 (2 CHLOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (2 FLUOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (2 METHOXYPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (2 NITROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (2,6 DICHLOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL] THIAZDOLIDIN 4 ONE; 2 (3 CHLOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (3 FLUOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (3 HYDROXYPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (3 METHOXYPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (3 NITROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (4 CHLOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (4 FLUOROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (4 HYDROXYPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (4 METHOXYPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 (4 NITROPHENYL) 3 [2 (PIPERIDIN 1 YL)ETHYL]THIAZOLIDIN 4 ONE; 2 ARYL 3 [(PIPERIDIN 1 YL)ETHYL]THIAZOLIDINONE DERIVATIVE; 3 [2 (PIPERIDIN 1 YL)ETHYL]2 4 TOLYLTHIAZOLIDIN 4 ONE; 4 THIAZOLIDINONE DERIVATIVE; ANTIFUNGAL AGENT; FLUCONAZOLE; HYDROGEN; UNCLASSIFIED DRUG;

EID: 84877028612     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.03.030     Document Type: Article
Times cited : (51)

References (36)
  • 2
    • 84857055939 scopus 로고    scopus 로고
    • Fungemia due to Rhodotorula mucilaginosa after allogeneic hematopoietic stem cell transplantation
    • T. Mori, Y. Nakamura, J. Kato, K. Sugita, M. Murata, K. Kamei, and S. Okamoto Fungemia due to Rhodotorula mucilaginosa after allogeneic hematopoietic stem cell transplantation Transpl. Infect. Dis. 14 2012 91 94
    • (2012) Transpl. Infect. Dis. , vol.14 , pp. 91-94
    • Mori, T.1    Nakamura, Y.2    Kato, J.3    Sugita, K.4    Murata, M.5    Kamei, K.6    Okamoto, S.7
  • 5
    • 84859402328 scopus 로고    scopus 로고
    • Azole-resistant Candida spp. - Emerging pathogens?
    • S. Tobudic, C. Kratzer, and E. Presterl Azole-resistant Candida spp. - emerging pathogens? Mycoses 55 2012 24 32
    • (2012) Mycoses , vol.55 , pp. 24-32
    • Tobudic, S.1    Kratzer, C.2    Presterl, E.3
  • 6
    • 23244447394 scopus 로고    scopus 로고
    • Emerging fungal diseases
    • DOI 10.1086/432060
    • M. Nucci, and K.A. Marr Emerging fungal diseases Clin. Infect. Dis. 41 2005 521 526 (Pubitemid 41099648)
    • (2005) Clinical Infectious Diseases , vol.41 , Issue.4 , pp. 521-526
    • Nucci, M.1    Marr, K.A.2
  • 7
    • 84055199809 scopus 로고    scopus 로고
    • Antifungal drug resistance: Mechanisms, epidemiology and consequences for treatment
    • M.A. Pfaller Antifungal drug resistance: mechanisms, epidemiology and consequences for treatment Am. J. Med. 125 2012 S3 S13
    • (2012) Am. J. Med. , vol.125
    • Pfaller, M.A.1
  • 8
    • 33750701101 scopus 로고    scopus 로고
    • Epidemiology and outcome of Rhodotorula fungemia in a tertiary care hospital
    • L.W. Lunardi, V.R. Aquino, R.A. Zimerman, and L.Z. Goldani Epidemiology and outcome of Rhodotorula fungemia in a tertiary care hospital Clin. Infect. Dis. 43 2006 e60 63
    • (2006) Clin. Infect. Dis. , vol.43 , pp. 60-63
    • Lunardi, L.W.1    Aquino, V.R.2    Zimerman, R.A.3    Goldani, L.Z.4
  • 10
    • 79958022139 scopus 로고    scopus 로고
    • Advances in synthetic approach to and antifungal activity of triazoles
    • K. Shalini, N. Kumar, S. Drabu, and P.K. Sharma Advances in synthetic approach to and antifungal activity of triazoles Beilstein J. Org. Chem. 7 2011 668 677
    • (2011) Beilstein J. Org. Chem. , vol.7 , pp. 668-677
    • Shalini, K.1    Kumar, N.2    Drabu, S.3    Sharma, P.K.4
  • 11
    • 84887825103 scopus 로고    scopus 로고
    • Design, synthesis and antimicrobial evaluation of novel 2-aryl-thiazolidin-4-one derivatives
    • D. Prasad, A. Kumar, P.K. Shukla, and M. Nath Design, synthesis and antimicrobial evaluation of novel 2-aryl-thiazolidin-4-one derivatives Org. Med. Chem. Lett. 1 2011 4/1 4/7
    • (2011) Org. Med. Chem. Lett. , vol.1
    • Prasad, D.1    Kumar, A.2    Shukla, P.K.3    Nath, M.4
  • 12
    • 84861188772 scopus 로고    scopus 로고
    • Recent developments and biological activities of thiazolidinone derivatives: A review
    • A.K. Jain, A. Vaidya, V. Ravichandran, S.K. Kashaw, and R.K. Agrawal Recent developments and biological activities of thiazolidinone derivatives: a review Bioorg. Med. Chem. 20 2012 3378 3395
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 3378-3395
    • Jain, A.K.1    Vaidya, A.2    Ravichandran, V.3    Kashaw, S.K.4    Agrawal, R.K.5
  • 13
    • 43049161063 scopus 로고    scopus 로고
    • Thiazolidinone - A biologically active scaffold
    • A. Verma, and S.K. Saraf Thiazolidinone - a biologically active scaffold Eur. J. Med. Chem. 43 2008 897 905
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 897-905
    • Verma, A.1    Saraf, S.K.2
  • 15
    • 84856011929 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some thiazolidinones as antimicrobial agents
    • D. Patel, P. Kumari, and N. Patel Synthesis and biological evaluation of some thiazolidinones as antimicrobial agents Eur. J. Med. Chem. 48 2012 354 362
    • (2012) Eur. J. Med. Chem. , vol.48 , pp. 354-362
    • Patel, D.1    Kumari, P.2    Patel, N.3
  • 16
    • 80053206950 scopus 로고    scopus 로고
    • Design, synthesis and HIV-RT inhibitory activity of novel thiazolidin-4-one derivatives
    • H. Chen, Z. Guo, Q. Yin, X. Duan, Y. Gu, and X. Li Design, synthesis and HIV-RT inhibitory activity of novel thiazolidin-4-one derivatives Front. Chem. Sci. Eng. 5 2011 231 237
    • (2011) Front. Chem. Sci. Eng. , vol.5 , pp. 231-237
    • Chen, H.1    Guo, Z.2    Yin, Q.3    Duan, X.4    Gu, Y.5    Li, X.6
  • 17
    • 79958296582 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of novel 4-thiazolidinones containing indolin-2-one moiety as potential antitumor agent
    • S. Wang, Y. Zhao, G. Zhang, Y. Lv, N. Zhang, and P. Gong Design, synthesis and biological evaluation of novel 4-thiazolidinones containing indolin-2-one moiety as potential antitumor agent Eur. J. Med. Chem. 46 2011 3509 3518
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 3509-3518
    • Wang, S.1    Zhao, Y.2    Zhang, G.3    Lv, Y.4    Zhang, N.5    Gong, P.6
  • 18
    • 84863189600 scopus 로고    scopus 로고
    • Synthesis, antioxidant and antimicrobial evaluation of thiazolidinone, azetidinone encompassing indolylthienopyrimidines
    • A.R. Saundane, M. Yarlakatti, P. Walmik, and V. Katkarf Synthesis, antioxidant and antimicrobial evaluation of thiazolidinone, azetidinone encompassing indolylthienopyrimidines J. Chem. Sci. 124 2012 469 481
    • (2012) J. Chem. Sci. , vol.124 , pp. 469-481
    • Saundane, A.R.1    Yarlakatti, M.2    Walmik, P.3    Katkarf, V.4
  • 19
    • 84866122547 scopus 로고    scopus 로고
    • Synthesis of 2-(aryl)-5-(arylidene)-4-thiazolidinone derivatives with potential analgesic and anti-inflammatory activity
    • A. Deep, S. Jain, P.C. Sharma, P. Phogat, and M. Malhotra Synthesis of 2-(aryl)-5-(arylidene)-4-thiazolidinone derivatives with potential analgesic and anti-inflammatory activity Med. Chem. Res. 21 2012 1652 1659
    • (2012) Med. Chem. Res. , vol.21 , pp. 1652-1659
    • Deep, A.1    Jain, S.2    Sharma, P.C.3    Phogat, P.4    Malhotra, M.5
  • 20
    • 84873995625 scopus 로고    scopus 로고
    • Synthesis and in vitro antimicrobial and anti-tubercular evaluation of some quinoline-based azitidinone and thiazolidinone analogues
    • B.M. Mistry, and S. Jauhari Synthesis and in vitro antimicrobial and anti-tubercular evaluation of some quinoline-based azitidinone and thiazolidinone analogues Med. Chem. Res. 22 2013 635 646
    • (2013) Med. Chem. Res. , vol.22 , pp. 635-646
    • Mistry, B.M.1    Jauhari, S.2
  • 21
    • 70449625291 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of novel N-alkyl/aryl substituted thiazolidinone arecoline analogues as muscarinic receptor 1 agonist in Alzheimer's dementia models
    • C.T. Sadashiva, J.N. Narenda Sharath Chandra, C.V. Kavitha, A. Thimmegowd, M.N. Subhash, and K.S. Rangappa Synthesis and pharmacological evaluation of novel N-alkyl/aryl substituted thiazolidinone arecoline analogues as muscarinic receptor 1 agonist in Alzheimer's dementia models Eur. J. Med. Chem. 44 2009 4848 4854
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 4848-4854
    • Sadashiva, C.T.1    Narenda Sharath Chandra, J.N.2    Kavitha, C.V.3    Thimmegowd, A.4    Subhash, M.N.5    Rangappa, K.S.6
  • 22
    • 32844468798 scopus 로고    scopus 로고
    • Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3H-indole-3,2′-thiazolidine]- 3′(1,2,4-triazol-3-yl)-2,4′(1H)-dione
    • DOI 10.1016/j.bmc.2005.11.025, PII S0968089605010904
    • A. Dandia, R. Singh, S. Khaturia, C. Merienne, G. Morgant, and A. Loupy Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro[indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3H-indole-3,2'-thiazolidine]-3'(1,2,4- triazol-3-yl)-2,4'(1H)-dione Bioorg. Med. Chem. 14 2006 2409 2417 (Pubitemid 43254748)
    • (2006) Bioorganic and Medicinal Chemistry , vol.14 , Issue.7 , pp. 2409-2417
    • Dandia, A.1    Singh, R.2    Khaturia, S.3    Merienne, C.4    Morgant, G.5    Loupy, A.6
  • 29
    • 50249160114 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of 1,3-thiazolidin-4-ones and 2-aryl-1,3-oxathiolan-5-ones
    • W. Cunico, W.T. Vellasco Junior, M. Moreth, and C.R.B. Gomes Microwave-assisted synthesis of 1,3-thiazolidin-4-ones and 2-aryl-1,3- oxathiolan-5-ones Lett. Org. Chem. 5 2008 349 352
    • (2008) Lett. Org. Chem. , vol.5 , pp. 349-352
    • Cunico, W.1    Vellasco Junior, W.T.2    Moreth, M.3    Gomes, C.R.B.4
  • 32
    • 33744971362 scopus 로고    scopus 로고
    • Synthesis, stereochemistry, and antimicrobial evaluation of substituted piperidin-4-one oxime ethers
    • C. Ramalingan, Y.T. Park, and S. Kabilan Synthesis, stereochemistry, and antimicrobial evaluation of substituted piperidin-4-one oxime ethers Eur. J. Med. Chem. 41 2006 683 696
    • (2006) Eur. J. Med. Chem. , vol.41 , pp. 683-696
    • Ramalingan, C.1    Park, Y.T.2    Kabilan, S.3
  • 33
    • 78149280918 scopus 로고    scopus 로고
    • Synthesis, antimicrobial evaluation and QSAR studies of novel piperidin-4-yl-5-spiro-thiadiazoline derivatives
    • S. Umamatheswari, B. Balaji, M. Ramanathan, and S. Kabilan Synthesis, antimicrobial evaluation and QSAR studies of novel piperidin-4-yl-5-spiro- thiadiazoline derivatives Bioorg. Med. Chem. Lett. 20 2010 6909 6914
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 6909-6914
    • Umamatheswari, S.1    Balaji, B.2    Ramanathan, M.3    Kabilan, S.4
  • 34
    • 80755143184 scopus 로고    scopus 로고
    • Antimicrobial activity and SAR study of some novel thiosemicarbazide derivatives bearing piperidine moiety
    • A. Siwek, and J. Stefanska Antimicrobial activity and SAR study of some novel thiosemicarbazide derivatives bearing piperidine moiety Med. Chem. 7 2011 690 696
    • (2011) Med. Chem. , vol.7 , pp. 690-696
    • Siwek, A.1    Stefanska, J.2
  • 36
    • 0022391554 scopus 로고
    • A simple quantitative procedure using monolayer cultures for cytotoxicity assays (HTD/NR-90)
    • DOI 10.1007/BF01666038
    • E. Borenfreund, and J.A. Puerner A simple quantitative procedure using monolayer culture for toxicity assays J. Tissue Cult. Methods 9 1985 7 9 (Pubitemid 15235618)
    • (1985) Journal of Tissue Culture Methods , vol.9 , Issue.1 , pp. 7-9
    • Borenfreund, E.1    Puerner, J.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.