메뉴 건너뛰기




Volumn 23, Issue 3, 2014, Pages 1612-1621

Synthesis, antimicrobial, and cytotoxicity studies of novel sulfur-linked quinoline-coumarin bisheterocycles

Author keywords

Antimicrobial activity; Coumarin; Cytotoxicity; Friedlander annulation; Quinoline

Indexed keywords


EID: 84893804430     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-013-0761-7     Document Type: Article
Times cited : (13)

References (15)
  • 1
    • 0035811449 scopus 로고    scopus 로고
    • Synthesis and antibacterial evaluation of certain quinolone derivatives
    • 1:CAS:528:DC%2BD3MXktFalsbg%3D 11428933 10.1021/jm0100335
    • Chen YL, Fang KC, Sheu JY, Hsu SL, Tzeng SS (2001) Synthesis and antibacterial evaluation of certain quinolone derivatives. J Med Chem 44:2374-2377
    • (2001) J Med Chem , vol.44 , pp. 2374-2377
    • Chen, Y.L.1    Fang, K.C.2    Sheu, J.Y.3    Hsu, S.L.4    Tzeng, S.S.5
  • 2
    • 39749084608 scopus 로고    scopus 로고
    • Structure-activity relationship of coumarin derivatives on xanthine oxidase-inhibiting and free radical-scavenging activities
    • 1:CAS:528:DC%2BD1cXislamtbk%3D 18201686 10.1016/j.bcp.2007.11.023
    • Lin HC, Tsai SH, Chen CS, Chang YC, Lee CM, Lai ZY, Lin CM (2008) Structure-activity relationship of coumarin derivatives on xanthine oxidase-inhibiting and free radical-scavenging activities. Biochem Pharmacol 75:1416-1425
    • (2008) Biochem Pharmacol , vol.75 , pp. 1416-1425
    • Lin, H.C.1    Tsai, S.H.2    Chen, C.S.3    Chang, Y.C.4    Lee, C.M.5    Lai, Z.Y.6    Lin, C.M.7
  • 3
    • 41749084640 scopus 로고    scopus 로고
    • Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide a analogues as anti-HIV-1 agents
    • 1:CAS:528:DC%2BD1cXitFeht7g%3D 18284187 10.1021/jm701405p
    • Ma T, Liu L, Xue H, Li L, Han C, Wang L, Chen Z, Liu G (2008) Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide a analogues as anti-HIV-1 agents. J Med Chem 51:1432-1446
    • (2008) J Med Chem , vol.51 , pp. 1432-1446
    • Ma, T.1    Liu, L.2    Xue, H.3    Li, L.4    Han, C.5    Wang, L.6    Chen, Z.7    Liu, G.8
  • 4
    • 0037971925 scopus 로고    scopus 로고
    • Novel coumarin derivatives of heterocyclic compounds as lipid-lowering agents
    • 1:CAS:528:DC%2BD3sXlt1WgsbY%3D 12852963 10.1016/S0960-894X(03)00490-6
    • Madhavan GR, Balraju V, Mallesham B, Chakrabarthi R, Lohray VB (2003) Novel coumarin derivatives of heterocyclic compounds as lipid-lowering agents. Bioorg Med Chem Lett 13:2547-2551
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 2547-2551
    • Madhavan, G.R.1    Balraju, V.2    Mallesham, B.3    Chakrabarthi, R.4    Lohray, V.B.5
  • 5
    • 0028217675 scopus 로고
    • Short synthesis of the dynemicin core structure: Unusual bridgehead enolate reactivity
    • 10.1039/c39940001543
    • Magnus P, Parry D, Illiadis T, Eisenbeis SA, Fairhuist RA (1994) Short synthesis of the dynemicin core structure: unusual bridgehead enolate reactivity. J Chem Soc Chem Commun 13:1543-1544
    • (1994) J Chem Soc Chem Commun , vol.13 , pp. 1543-1544
    • Magnus, P.1    Parry, D.2    Illiadis, T.3    Eisenbeis, S.A.4    Fairhuist, R.A.5
  • 6
    • 0030047733 scopus 로고    scopus 로고
    • Total synthesis of (-)-tetrahydropalmatine via chiral formamidine carbanions:unexpected behavior with certain ortho-substituted electrophiles
    • 1:CAS:528:DyaK28Xis1Krsw%3D%3D 11666977 10.1021/jo951611q
    • Matulenko MA, Meyers AI (1996) Total synthesis of (-)-tetrahydropalmatine via chiral formamidine carbanions:unexpected behavior with certain ortho-substituted electrophiles. J Org Chem 61:573-580
    • (1996) J Org Chem , vol.61 , pp. 573-580
    • Matulenko, M.A.1    Meyers, A.I.2
  • 8
    • 47749108003 scopus 로고    scopus 로고
    • Synthesis of a new class of bisheterocycles from phenacylsulfonylacetic acid methyl ester
    • 1:CAS:528:DC%2BD1cXoslymt74%3D 10.1002/jhet.5570450430
    • Padmavathi V, Mohan AVN, Mahesh K (2008) Synthesis of a new class of bisheterocycles from phenacylsulfonylacetic acid methyl ester. J Heterocycl Chem 45:1131-1138
    • (2008) J Heterocycl Chem , vol.45 , pp. 1131-1138
    • Padmavathi, V.1    Mohan, A.V.N.2    Mahesh, K.3
  • 9
    • 0032900708 scopus 로고    scopus 로고
    • A cycloaddition approach toward the synthesis of substituted indolines and tetrahydroquinolines
    • 1:CAS:528:DyaK1MXivFyltbw%3D 11674487 10.1021/jo982453g
    • Padwa A, Brodney MA, Liu B, Satake K, Wu T (1999) A cycloaddition approach toward the synthesis of substituted indolines and tetrahydroquinolines. J Org Chem 64:3595-3607
    • (1999) J Org Chem , vol.64 , pp. 3595-3607
    • Padwa, A.1    Brodney, M.A.2    Liu, B.3    Satake, K.4    Wu, T.5
  • 10
    • 84856641119 scopus 로고    scopus 로고
    • Camphorsulfonic acid catalysed facile tandem double Friedlander annulation protocol for the synthesis of phenoxy linked bisquinoline derivatives and discovery of antitubercular agents
    • 1:CAS:528:DC%2BC38XitVWrt7Y%3D 22277278 10.1016/j.bmcl.2011.12.119
    • Paul N, Murugavel M, Muthusubramanian S, Sriram D (2012) Camphorsulfonic acid catalysed facile tandem double Friedlander annulation protocol for the synthesis of phenoxy linked bisquinoline derivatives and discovery of antitubercular agents. Bioorg Med Chem Lett 22:1643-1648
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 1643-1648
    • Paul, N.1    Murugavel, M.2    Muthusubramanian, S.3    Sriram, D.4
  • 11
    • 77958067742 scopus 로고    scopus 로고
    • Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives
    • 1:CAS:528:DC%2BC3cXhtlSms7bJ 20932744 10.1016/j.bmcl.2010.09.055
    • Sashidhara KV, Kumar A, Kumar M, Srivastava A, Puri A (2010) Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives. Bioorg Med Chem Lett 20:6504-6507
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 6504-6507
    • Sashidhara, K.V.1    Kumar, A.2    Kumar, M.3    Srivastava, A.4    Puri, A.5
  • 12
    • 33846458645 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives
    • 1:CAS:528:DC%2BD28XhtlKjsrvL 17228883 10.1021/jm061002i
    • Solomon VR, Haq W, Srivastava K, Puri SK, Katti SB (2007) Synthesis and antimalarial activity of side chain modified 4-aminoquinoline derivatives. J Med Chem 50:394-398
    • (2007) J Med Chem , vol.50 , pp. 394-398
    • Solomon, V.R.1    Haq, W.2    Srivastava, K.3    Puri, S.K.4    Katti, S.B.5
  • 13
    • 70349270651 scopus 로고    scopus 로고
    • Practical synthesis of maleimides and coumarin-linked probes for protein and anti body labelling via reduction of native disulfides
    • 1:CAS:528:DC%2BD1MXpsl2itrw%3D 19675893 10.1039/b904060a
    • Song HY, Ngai MH, Song ZY, MacAry PA, Hobley J, Lear MJ (2009) Practical synthesis of maleimides and coumarin-linked probes for protein and anti body labelling via reduction of native disulfides. Org Biomol Chem 7:3400-3406
    • (2009) Org Biomol Chem , vol.7 , pp. 3400-3406
    • Song, H.Y.1    Ngai, M.H.2    Song, Z.Y.3    Macary, P.A.4    Hobley, J.5    Lear, M.J.6
  • 15
    • 27944434132 scopus 로고    scopus 로고
    • Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin-resveratrol hybrids
    • 1:CAS:528:DC%2BD2MXht1Git7bN 16275073 10.1016/j.bmcl.2005.10.013
    • Vilar S, Quezada E, Santana L, Uriarte E, Yanez M, Fraiz N, Alcalde C, Cano E, Orallo F (2006) Design, synthesis, and vasorelaxant and platelet antiaggregatory activities of coumarin-resveratrol hybrids. Bioorg Med Chem Lett 16:257-261
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 257-261
    • Vilar, S.1    Quezada, E.2    Santana, L.3    Uriarte, E.4    Yanez, M.5    Fraiz, N.6    Alcalde, C.7    Cano, E.8    Orallo, F.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.