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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

228 related items for PubMed ID: 15018918

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  • 2. Antimycobacterial compounds. Optimization of the BM 212 structure, the lead compound for a new pyrrole derivative class.
    Biava M, Porretta GC, Poce G, Deidda D, Pompei R, Tafi A, Manetti F.
    Bioorg Med Chem; 2005 Feb 15; 13(4):1221-30. PubMed ID: 15670931
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  • 4. 1,5-Diphenylpyrrole derivatives as antimycobacterial agents. Probing the influence on antimycobacterial activity of lipophilic substituents at the phenyl rings.
    Biava M, Porretta GC, Poce G, De Logu A, Saddi M, Meleddu R, Manetti F, De Rossi E, Botta M.
    J Med Chem; 2008 Jun 26; 51(12):3644-8. PubMed ID: 18494459
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  • 5. Importance of the thiomorpholine introduction in new pyrrole derivatives as antimycobacterial agents analogues of BM 212.
    Biava M, Cesare Porretta G, Deidda D, Pompei R, Tafi A, Manetti F.
    Bioorg Med Chem; 2003 Feb 20; 11(4):515-20. PubMed ID: 12538016
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  • 6. Antimycobacterial agents. Novel diarylpyrrole derivatives of BM212 endowed with high activity toward Mycobacterium tuberculosis and low cytotoxicity.
    Biava M, Porretta GC, Poce G, Supino S, Deidda D, Pompei R, Molicotti P, Manetti F, Botta M.
    J Med Chem; 2006 Aug 10; 49(16):4946-52. PubMed ID: 16884306
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  • 7. New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold.
    Biava M, Porretta GC, Manetti F.
    Mini Rev Med Chem; 2007 Jan 10; 7(1):65-78. PubMed ID: 17266639
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  • 10. Design and Synthesis of 1-((1,5-Bis(4-chlorophenyl)-2-methyl-1H-pyrrol-3-yl)methyl)-4-methylpiperazine (BM212) and N-Adamantan-2-yl-N'-((E)-3,7-dimethylocta-2,6-dienyl)ethane-1,2-diamine (SQ109) Pyrrole Hybrid Derivatives: Discovery of Potent Antitubercular Agents Effective against Multidrug-Resistant Mycobacteria.
    Bhakta S, Scalacci N, Maitra A, Brown AK, Dasugari S, Evangelopoulos D, McHugh TD, Mortazavi PN, Twist A, Petricci E, Manetti F, Castagnolo D.
    J Med Chem; 2016 Mar 24; 59(6):2780-93. PubMed ID: 26907951
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  • 11. Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity.
    Wavhale RD, Martis EAF, Ambre PK, Wan B, Franzblau SG, Iyer KR, Raikuvar K, Macegoniuk K, Berlicki Ł, Nandan SR, Coutinho EC.
    Bioorg Med Chem; 2017 Sep 01; 25(17):4835-4844. PubMed ID: 28778369
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  • 12. Synthesis and antimicrobial activity of some pyrrole derivatives. V: 5-Aryl-3-ethoxycarbonyl-2-(4-substituted piperazino)pyrrole derivatives.
    Cocco MT, Onnis V, Schivo ML, De Logu A.
    Farmaco; 1992 Nov 01; 47(11):1395-405. PubMed ID: 1492903
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  • 13. Synthesis and antimicrobial activity of some pyrrole derivatives. III--2-(4-arylpiperazino)-3-ethoxycarbonyl-5-aryl-pyrrole derivatives.
    Cocco MT, Congiu C, Maccioni A, Schivo ML, De Logu A, Palmieri G.
    Farmaco Sci; 1988 Dec 01; 43(12):951-60. PubMed ID: 3248594
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  • 14. In vitro and ex vivo activity of new derivatives of acetohydroxyacid synthase inhibitors against Mycobacterium tuberculosis and non-tuberculous mycobacteria.
    Sohn H, Lee KS, Ko YK, Ryu JW, Woo JC, Koo DW, Shin SJ, Ahn SJ, Shin AR, Song CH, Jo EK, Park JK, Kim HJ.
    Int J Antimicrob Agents; 2008 Jun 01; 31(6):567-71. PubMed ID: 18337064
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  • 15. Design and synthesis of novel carbazole tethered pyrrole derivatives as potent inhibitors of Mycobacterium tuberculosis.
    Surineni G, Yogeeswari P, Sriram D, Kantevari S.
    Bioorg Med Chem Lett; 2015 Feb 01; 25(3):485-91. PubMed ID: 25559743
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  • 16. Developing pyrrole-derived antimycobacterial agents: a rational lead optimization approach.
    Biava M, Porretta GC, Poce G, Battilocchio C, Alfonso S, de Logu A, Manetti F, Botta M.
    ChemMedChem; 2011 Apr 04; 6(4):593-9. PubMed ID: 21341373
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  • 19. 2(3H)-furanones and 2(3H)-pyrrolones: synthesis and antimycobacterial evaluation.
    Husain A, Alam MM, Hasan SM, Yar MS.
    Acta Pol Pharm; 2009 Apr 04; 66(2):173-80. PubMed ID: 19719052
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