메뉴 건너뛰기




Volumn 22, Issue 2, 2013, Pages 758-767

Synthesis, characterization, anticancer, and antioxidant activity of some new thiazolidin-4-ones in MCF-7 cells

Author keywords

Antioxidant activity; Cytotoxicity; DNA fragmentation; Thiazolidin 4 one

Indexed keywords

2 [3 (4 CHLOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 (2 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 CHLOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 (4 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 CHLOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 (PHENOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 CHLOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 [(NAPHTHALEN 1 YLOXY)METHYL] 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 CHLOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 [(NAPHTHALEN 2 YLOXY)] 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 FLUOROPHENYL) 1H PYRAZOL 4 YL] 3 (3 MERCAPTO 5 (2 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 FLUOROPHENYL) 1H PYRAZOL 4 YL] 3 (3 MERCAPTO 5 (4 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 FLUOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 (PHENOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 FLUOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 [(NAPHTHALEN 1YLOXY)]METHYL] 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 2 [3 (4 FLUOROPHENYL) 1H PYRAZOL 4 YL] 3 [3 MERCAPTO 5 [(NAPHTHALEN 2 YLOXY)METHYL] 4H 1,2,4 TRIAZOL 4 YL]THIAZOLIDIN 4 ONE; 3 [3 MERCAPTO 5 (2 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL] 2 [3 (4 METHOXYPHENYL) 1H PYRAZOL 4 YL]THIAZOLIDIN 4 ONE; 3 [3 MERCAPTO 5 (4 TOLYLOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL] 2 [3 (4 METHOXYPHENYL) 1H PYRAZOL 4 YL]THIAZOLIDIN 4 ONE; 3 [3 MERCAPTO 5 (PHENOXYMETHYL) 4H 1,2,4 TRIAZOL 4 YL] 2 [3 (4 METHOXYPHENYL) 1H PYRAZOL 4 YL]THIAZOLIDIN 4 ONE; 3 [3 MERCAPTO 5 [(NAPHTHALEN 1 YLOXY)METHYL] 4H 1,2,4 TRIAZOL 4 YL] 2 [3 (4 METHOXYPHENYL) 1H PYRAZOL 4 YL]THIAZOLIDIN 4 ONE; 3 [3 MERCAPTO 5 [(NAPHTHALEN 2 YLOXY)METHYL] 4H 1,2,4 TRIAZOL 4 YL] 2 [3 (4 METHOXYPHENYL) 1H PYRAZOL 4 YL]THIAZOLIDIN 4 ONE; ANTINEOPLASTIC AGENT; ANTIOXIDANT; ASCORBIC ACID; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84873991174     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-012-0071-5     Document Type: Article
Times cited : (48)

References (31)
  • 1
    • 18244393983 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some 4-thiazolidinones
    • 1:CAS:528:DC%2BD2MXot12ksg%3D%3D
    • Amir M, Azam F (2004) Synthesis and biological evaluation of some 4-thiazolidinones. Indian J Heterocycl Chem 14:119-122
    • (2004) Indian J Heterocycl Chem , vol.14 , pp. 119-122
    • Amir, M.1    Azam, F.2
  • 2
    • 72149083045 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a novel series of pyrazole chalcones as anti-inflammatory, antioxidant and antimicrobial agents
    • 19896853 10.1016/j.bmc.2009.10.035 1:CAS:528:DC%2BD1MXhsVajsbnJ
    • Bandgar PB, Gawande SS, Bodade RG, Gawande NM, Khobragade CN (2009) Synthesis and biological evaluation of a novel series of pyrazole chalcones as anti-inflammatory, antioxidant and antimicrobial agents. Bioorg Med Chem 17:8168-8173
    • (2009) Bioorg Med Chem , vol.17 , pp. 8168-8173
    • Bandgar, P.B.1    Gawande, S.S.2    Bodade, R.G.3    Gawande, N.M.4    Khobragade, C.N.5
  • 3
    • 75149145989 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents
    • 20064725 10.1016/j.bmc.2009.11.066 1:CAS:528:DC%2BC3cXhtlGisbY%3D
    • Bandgar PB, Gawande SS, Bodade RG, Totre JV, Khobragade CN (2010) Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents. Bioorg Med Chem 18:1364-1370
    • (2010) Bioorg Med Chem , vol.18 , pp. 1364-1370
    • Bandgar, P.B.1    Gawande, S.S.2    Bodade, R.G.3    Totre, J.V.4    Khobragade, C.N.5
  • 4
    • 18844443185 scopus 로고    scopus 로고
    • Aromatase inhibitors in the treatment of breast cancer
    • 10.1210/er.2004-0015
    • Brueggemeier RW, John CH, Edgar SD (2004) Aromatase inhibitors in the treatment of breast cancer. Endocrine Rev 26:331-345
    • (2004) Endocrine Rev , vol.26 , pp. 331-345
    • Brueggemeier, R.W.1    John, C.H.2    Edgar, S.D.3
  • 5
    • 84866391524 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial activity of novel ethyl 1-(N-substituted)-5-phenyl-1H-pyrazole-4-carboxylate derivatives
    • doi: 10.1007/s00044-011-9796-9
    • Chandrakantha B, Isloor AM, Shetty P, Isloor S, Malladi S, Fun HK (2011) Synthesis, characterization and antimicrobial activity of novel ethyl 1-(N-substituted)-5-phenyl-1H-pyrazole-4-carboxylate derivatives. Med Chem Res. doi: 10.1007/s00044-011-9796-9
    • (2011) Med Chem Res
    • Chandrakantha, B.1    Isloor, A.M.2    Shetty, P.3    Isloor, S.4    Malladi, S.5    Fun, H.K.6
  • 6
    • 4444270755 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of some new 1-(5-phenylamino-[1,3, 4]thiadiazol-2-yl)methyl-5-oxo-[1,2,4]triazole and 1-(4-phenyl-5-thioxo-[1,2,4] triazole-3-yl)methyl-5-oxo[1,2,4]triazole derivatives
    • 15337292 10.1016/j.ejmech.2004.06.007 1:CAS:528:DC%2BD2cXntVOhuro%3D
    • Demirbas N, Karaoglu SA, Demirbas A, Sanack K (2004) Synthesis and antimicrobial activities of some new 1-(5-phenylamino-[1,3,4]thiadiazol-2-yl) methyl-5-oxo-[1,2,4]triazole and 1-(4-phenyl-5-thioxo-[1,2,4] triazole-3-yl)methyl-5-oxo[1,2,4]triazole derivatives. Eur J Med Chem 39:793-804
    • (2004) Eur J Med Chem , vol.39 , pp. 793-804
    • Demirbas, N.1    Karaoglu, S.A.2    Demirbas, A.3    Sanack, K.4
  • 7
    • 24644484422 scopus 로고    scopus 로고
    • AK-2123 (Sanazol) as a radiation sensitizer in the treatment of stage III cancer cervix: Initial results of an IAEA multicentre randomized trial
    • 17998631 10.4103/0973-1482.16705 1:CAS:528:DC%2BD28XivV2rsLw%3D
    • Dobrowsky W, Huigol NG, Jayatilake RS, Kizilbash NI, Okkan S, Kagiya TV, Tatsuzaki H (2005) AK-2123 (Sanazol) as a radiation sensitizer in the treatment of stage III cancer cervix: initial results of an IAEA multicentre randomized trial. J Cancer Res Ther 1:75-78
    • (2005) J Cancer Res Ther , vol.1 , pp. 75-78
    • Dobrowsky, W.1    Huigol, N.G.2    Jayatilake, R.S.3    Kizilbash, N.I.4    Okkan, S.5    Kagiya, T.V.6    Tatsuzaki, H.7
  • 8
    • 67649909614 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of substituted triazolo[4,3-a]pyrimidin- 6-sulfonamide with an incorporated thiazolidinone moiety
    • 19540114 10.1016/j.bmcl.2009.05.126 1:CAS:528:DC%2BD1MXosVGmtrk%3D
    • Hafez HN, El-Gazzar ABA (2009) Synthesis and antitumor activity of substituted triazolo[4,3-a]pyrimidin-6-sulfonamide with an incorporated thiazolidinone moiety. Bioorg Med Chem Lett 19:4143-4147
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 4143-4147
    • Hafez, H.N.1    El-Gazzar, A.B.A.2
  • 9
    • 0036592243 scopus 로고    scopus 로고
    • New bis-aminomercaptotriazoles and bis-triazolothiadiazoles as possible anticancer agents
    • 12204477 10.1016/S0223-5234(02)01358-2
    • Holla BS, Poojary KN, Rao BS, Shivananda MK (2002) New bis-aminomercaptotriazoles and bis-triazolothiadiazoles as possible anticancer agents. Eur J Med Chem 37:511-517
    • (2002) Eur J Med Chem , vol.37 , pp. 511-517
    • Holla, B.S.1    Poojary, K.N.2    Rao, B.S.3    Shivananda, M.K.4
  • 10
    • 67349255332 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 3,6-disubstituted [1,2,4] triazolo[3,4-b][1,3,4]thiadiazole derivatives as a novel class of potential anti-tumor agents
    • 19203813 10.1016/j.ejmech.2009.01.003 1:CAS:528:DC%2BD1MXltl2lt78%3D
    • Ibrahim DA (2009) Synthesis and biological evaluation of 3,6-disubstituted [1,2,4] triazolo[3,4-b][1,3,4]thiadiazole derivatives as a novel class of potential anti-tumor agents. Eur J Med Chem 44:2776-2781
    • (2009) Eur J Med Chem , vol.44 , pp. 2776-2781
    • Ibrahim, D.A.1
  • 11
    • 67650429659 scopus 로고    scopus 로고
    • Regioselective reaction: Synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles
    • 19464087 10.1016/j.ejmech.2009.04.038 1:CAS:528:DC%2BD1MXoslGhsLk%3D
    • Isloor AM, Kalluraya B, Shetty P (2009) Regioselective reaction: synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles. Eur J Med Chem 44:3784-3787
    • (2009) Eur J Med Chem , vol.44 , pp. 3784-3787
    • Isloor, A.M.1    Kalluraya, B.2    Shetty, P.3
  • 13
    • 0036137529 scopus 로고    scopus 로고
    • Doxorubicin-induced apoptosis and chemosensitivity in hepatoma cell lines
    • 11855756 10.1007/s00280-001-0376-4 1:CAS:528:DC%2BD3MXptFCksr4%3D
    • Lee T, Lau T, Ng I (2002) Doxorubicin-induced apoptosis and chemosensitivity in hepatoma cell lines. Cancer Chemother Pharmacol 49:78-86
    • (2002) Cancer Chemother Pharmacol , vol.49 , pp. 78-86
    • Lee, T.1    Lau, T.2    Ng, I.3
  • 14
    • 84878986364 scopus 로고    scopus 로고
    • Synthesis, characterization and ntibacterial activity of some new pyrazole based Schiff bases
    • doi: 10.1016/j.arabjc.2011.10.009
    • Malladi S, Isloor AM, Isloor S, Akhila DS (2011a) Synthesis, characterization and ntibacterial activity of some new pyrazole based Schiff bases. Arabian J Chem. doi: 10.1016/j.arabjc.2011.10.009
    • (2011) Arabian J Chem
    • Malladi, S.1    Isloor, A.M.2    Isloor, S.3    Akhila, D.S.4
  • 15
    • 84866416420 scopus 로고    scopus 로고
    • Synthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety
    • doi: 10.1007/s00044-011-9865-0
    • Malladi S, Isloor AM, Shetty P, Fun HK, Telkar S, Mahmood R, Isloor N (2011b) Synthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety. Med Chem Res. doi: 10.1007/s00044-011-9865-0
    • (2011) Med Chem Res
    • Malladi, S.1    Isloor, A.M.2    Shetty, P.3    Fun, H.K.4    Telkar, S.5    Mahmood, R.6    Isloor, N.7
  • 16
    • 34249660531 scopus 로고    scopus 로고
    • Studies on synthesis and pharmacological activities of 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and their dihydro analogues
    • 17331622 10.1016/j.ejmech.2006.12.010 1:CAS:528:DC%2BD2sXmtVahsb4%3D
    • Mathew V, Keshavayya J, Vaidya VP, Giles D (2007) Studies on synthesis and pharmacological activities of 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4- thiadiazoles and their dihydro analogues. Eur J Med Chem 42:823-840
    • (2007) Eur J Med Chem , vol.42 , pp. 823-840
    • Mathew, V.1    Keshavayya, J.2    Vaidya, V.P.3    Giles, D.4
  • 17
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxic assays
    • 10.1016/0022-1759(83)90303-4 1:STN:280:DyaL2c%2FovFSmtw%3D%3D
    • Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxic assays. Immunol Methods 65:55-63
    • (1983) Immunol Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 18
    • 62549153106 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles
    • 19036476 10.1016/j.ejmech.2008.10.012 1:CAS:528:DC%2BD1MXjsl2gsrY%3D
    • Padmavathi V, Reddy GS, Padmaja A, Kondaiah P, Ali-Shazia (2009) Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles. Eur J Med Chem 44:2106-2112
    • (2009) Eur J Med Chem , vol.44 , pp. 2106-2112
    • Padmavathi, V.1    Reddy, G.S.2    Padmaja, A.3    Kondaiah, P.4    Ali-Shazia5
  • 19
    • 70450224258 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of some novel bis-1,2,4-triazolo[3, 4-b]-1,3,4-thiadiazoles and bis-4-thiazolidinone derivatives from terephthalic dihydrazide
    • 19683841 10.1016/j.ejmech.2009.07.023 1:CAS:528:DC%2BD1MXhsVCksb7I
    • Palekar VS, Damle AJ, Shukla SR (2009) Synthesis and antibacterial activity of some novel bis-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and bis-4-thiazolidinone derivatives from terephthalic dihydrazide. Eur J Med Chem 44:5112-5116
    • (2009) Eur J Med Chem , vol.44 , pp. 5112-5116
    • Palekar, V.S.1    Damle, A.J.2    Shukla, S.R.3
  • 20
    • 38349038425 scopus 로고    scopus 로고
    • Westernizing women's risks? Breast cancer in lower-income countries
    • 18199859 10.1056/NEJMp0708307 1:CAS:528:DC%2BD1cXms1Ogug%3D%3D
    • Porter P (2008) Westernizing women's risks? Breast cancer in lower-income countries. N Engl J Med 358:213-216
    • (2008) N Engl J Med , vol.358 , pp. 213-216
    • Porter, P.1
  • 21
    • 43049122412 scopus 로고    scopus 로고
    • Synthesis of 2-[3′(2′-chloroquinolinyl)-3-carbethoxymethyl]- 4-thiazolidinones
    • 1:CAS:528:DC%2BD1cXitFajs78%3D
    • Selvi G, Rajendran SP (2007) Synthesis of 2-[3′(2′- chloroquinolinyl)-3-carbethoxymethyl]-4-thiazolidinones. Indian J Het Chem 17:201-202
    • (2007) Indian J Het Chem , vol.17 , pp. 201-202
    • Selvi, G.1    Rajendran, S.P.2
  • 22
    • 34548627498 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant screening of 2-(substituted aryl)-3-(4H-1,2,4-triazol-4-yl)-1,3-thiazolidinon-4-ones
    • Siddiqui N, Deepanjali, Md Arshad F, Rana A (2007) Synthesis and anticonvulsant screening of 2-(substituted aryl)-3-(4H-1,2,4-triazol-4-yl)-1,3- thiazolidinon-4-ones. Indian J Het Chem 16:403-404
    • (2007) Indian J Het Chem , vol.16 , pp. 403-404
    • Siddiqui, N.1    Deepanjali2    Md Arshad, F.3    Rana, A.4
  • 23
    • 0034693836 scopus 로고    scopus 로고
    • Microgels for estimation of DNA strand breaks, DNA protein cross links and apoptosis
    • 11113471 10.1016/S0027-5107(00)00075-0 1:CAS:528:DC%2BD3cXoslGhtrY%3D
    • Singh NP (2000) Microgels for estimation of DNA strand breaks, DNA protein cross links and apoptosis. Mutation Res 455:111-127
    • (2000) Mutation Res , vol.455 , pp. 111-127
    • Singh, N.P.1
  • 24
    • 0029935490 scopus 로고    scopus 로고
    • Free radical scavenging activity of curcuminoids
    • 1:CAS:528:DyaK28XhvFOqsbg%3D
    • Sreejayan N, Rao MN (1996) Free radical scavenging activity of curcuminoids. Drug Res 46:169-171
    • (1996) Drug Res , vol.46 , pp. 169-171
    • Sreejayan, N.1    Rao, M.N.2
  • 25
    • 85027926561 scopus 로고    scopus 로고
    • Synthesis, characterization and in vitro cytotoxic properties of some new Schiff and Mannich bases in Hep G2 cells
    • 10.1007/s00044-010-9433-z 1:CAS:528:DC%2BC3cXht1WgtrjE
    • Sunil D, Isloor AM, Shetty P, Chandrakantha B, Satyamoorthy K (2011) Synthesis, characterization and in vitro cytotoxic properties of some new Schiff and Mannich bases in Hep G2 cells. Med Chem Res 20:1024-1032
    • (2011) Med Chem Res , vol.20 , pp. 1024-1032
    • Sunil, D.1    Isloor, A.M.2    Shetty, P.3    Chandrakantha, B.4    Satyamoorthy, K.5
  • 26
    • 33646138015 scopus 로고    scopus 로고
    • Synthesis of pharmaceutically important condensed heterocyclic 4,6-disubstituted-1,2,4-triazolo-1,3,4-thiadiazole derivatives as antimicrobials
    • 16529848 10.1016/j.ejmech.2005.12.009 1:CAS:528:DC%2BD28Xkt1yjsbY%3D
    • Swamy SN, Basappa, Priya BS, Prabhuswamy B, Doreswamy BH, Prasad JS, Rangappa KS (2006) Synthesis of pharmaceutically important condensed heterocyclic 4,6-disubstituted-1,2,4-triazolo-1,3,4-thiadiazole derivatives as antimicrobials. Eur J Med Chem 41:531-538
    • (2006) Eur J Med Chem , vol.41 , pp. 531-538
    • Swamy, S.N.1    Basappa2    Priya, B.S.3    Prabhuswamy, B.4    Doreswamy, B.H.5    Prasad, J.S.6    Rangappa, K.S.7
  • 27
    • 54249121686 scopus 로고    scopus 로고
    • In vitro antioxidant activity of Enicostemmaaxillare
    • 10.1248/jhs.54.524 1:CAS:528:DC%2BD1cXht1Shu7nM
    • Vaijanathappa J, Badami S, Bhojraj S (2008) In vitro antioxidant activity of Enicostemmaaxillare. J Health Sci 54:524-528
    • (2008) J Health Sci , vol.54 , pp. 524-528
    • Vaijanathappa, J.1    Badami, S.2    Bhojraj, S.3
  • 28
    • 77957854410 scopus 로고    scopus 로고
    • Synthesis, characterization and anti-microbial studies of some novel 2,4-disubstituted thiazoles
    • 20716467 10.1016/j.ejmech.2010.07.048 1:CAS:528:DC%2BC3cXht1Krt7%2FP
    • Vijesh AM, Isloor AM, Prabhu V, Ahmad S, Malladi S (2010) Synthesis, characterization and anti-microbial studies of some novel 2,4-disubstituted thiazoles. Eur J Med Chem 45:5460-5464
    • (2010) Eur J Med Chem , vol.45 , pp. 5460-5464
    • Vijesh, A.M.1    Isloor, A.M.2    Prabhu, V.3    Ahmad, S.4    Malladi, S.5
  • 29
    • 79958258686 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial studies of some new pyrazole incorporated imidazole derivatives
    • 21620535 10.1016/j.ejmech.2011.05.005 1:CAS:528:DC%2BC3MXnsVeqsrg%3D
    • Vijesh AM, Isloor AM, Telkar S, Peethambar SK, Rai S, Isloor N (2011a) Synthesis, characterization and antimicrobial studies of some new pyrazole incorporated imidazole derivatives. Eur J Med Chem 46:3531-3536
    • (2011) Eur J Med Chem , vol.46 , pp. 3531-3536
    • Vijesh, A.M.1    Isloor, A.M.2    Telkar, S.3    Peethambar, S.K.4    Rai, S.5    Isloor, N.6
  • 30
    • 80054941845 scopus 로고    scopus 로고
    • Hantzsch reaction: Synthesis and characterization of some new 1,4-dihydropyridine derivatives as potent antimicrobial and antioxidant agents
    • 21968373 10.1016/j.ejmech.2011.09.026 1:CAS:528:DC%2BC3MXhtlKkurzF
    • Vijesh AM, Isloor AM, Peethambar SK, Shivananda KN, Arulmoli T, Isloor NA (2011b) Hantzsch reaction: synthesis and characterization of some new 1,4-dihydropyridine derivatives as potent antimicrobial and antioxidant agents. Eur J Med Chem 46:5591-5597
    • (2011) Eur J Med Chem , vol.46 , pp. 5591-5597
    • Vijesh, A.M.1    Isloor, A.M.2    Peethambar, S.K.3    Shivananda, K.N.4    Arulmoli, T.5    Isloor, N.A.6
  • 31
    • 57249116162 scopus 로고    scopus 로고
    • Chemistry and biological activities of 1,3-thiazolidin-4-ones
    • 10.2174/157019308786242232
    • Wilson C, Gomes CRB, Vellasco WT (2008) Chemistry and biological activities of 1,3-thiazolidin-4-ones. Mini-Rev Org Chem 5:336-344
    • (2008) Mini-Rev Org Chem , vol.5 , pp. 336-344
    • Wilson, C.1    Gomes, C.R.B.2    Vellasco, W.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.