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Journal Abstract Search

321 related items for PubMed ID: 25827525

  • 1. Synthesis and biological evaluation of 2-arylbenzimidazoles targeting Leishmania donovani.
    Keurulainen L, Siiskonen A, Nasereddin A, Kopelyanskiy D, Sacerdoti-Sierra N, Leino TO, Tammela P, Yli-Kauhaluoma J, Jaffe CL, Kiuru P.
    Bioorg Med Chem Lett; 2015 May 01; 25(9):1933-7. PubMed ID: 25827525
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  • 2. Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents.
    Marrapu VK, Mittal M, Shivahare R, Gupta S, Bhandari K.
    Eur J Med Chem; 2011 May 01; 46(5):1694-700. PubMed ID: 21385661
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  • 3. Design, synthesis and biological evaluation of aryl pyrimidine derivatives as potential leishmanicidal agents.
    Suryawanshi SN, Kumar S, Shivahare R, Pandey S, Tiwari A, Gupta S.
    Bioorg Med Chem Lett; 2013 Sep 15; 23(18):5235-8. PubMed ID: 23910597
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  • 4. Synthesis, antileishmanial and antitrypanosomal activities of N-substituted tetrahydro-β-carbolines.
    Manda S, Khan SI, Jain SK, Mohammed S, Tekwani BL, Khan IA, Vishwakarma RA, Bharate SB.
    Bioorg Med Chem Lett; 2014 Aug 01; 24(15):3247-50. PubMed ID: 24980054
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  • 6. Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines.
    Sunduru N, Nishi, Palne S, Chauhan PM, Gupta S.
    Eur J Med Chem; 2009 Jun 01; 44(6):2473-81. PubMed ID: 19217698
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  • 8. Arylanthranilodinitriles: a new biaryl class of antileishmanial agents.
    Singh FV, Vatsyayan R, Roy U, Goel A.
    Bioorg Med Chem Lett; 2006 May 15; 16(10):2734-7. PubMed ID: 16503140
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  • 9. Synthesis and biological evaluation of 2,3-dihydroimidazo[1,2-a]benzimidazole derivatives against Leishmania donovani and Trypanosoma cruzi.
    Oh S, Kim S, Kong S, Yang G, Lee N, Han D, Goo J, Siqueira-Neto JL, Freitas-Junior LH, Song R.
    Eur J Med Chem; 2014 Sep 12; 84():395-403. PubMed ID: 25036797
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  • 10. Synthesis of chromenochalcones and evaluation of their in vitro antileishmanial activity.
    Narender T, Khaliq T, Shweta, Nishi, Goyal N, Gupta S.
    Bioorg Med Chem; 2005 Dec 01; 13(23):6543-50. PubMed ID: 16185885
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  • 11. Synthesis and antiprotozoal activity of original porphyrin precursors and derivatives.
    Abada Z, Cojean S, Pomel S, Ferrié L, Akagah B, Lormier AT, Loiseau PM, Figadère B.
    Eur J Med Chem; 2013 Sep 01; 67():158-65. PubMed ID: 23851117
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  • 12. Antileishmanial ferrocenylquinoline derivatives: Synthesis and biological evaluation against Leishmania donovani.
    Yousuf M, Mukherjee D, Dey S, Pal C, Adhikari S.
    Eur J Med Chem; 2016 Nov 29; 124():468-479. PubMed ID: 27598235
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  • 14. Syntheses of new substituted triazino tetrahydroisoquinolines and beta-carbolines as novel antileishmanial agents.
    Kumar A, Katiyar SB, Gupta S, Chauhan PM.
    Eur J Med Chem; 2006 Jan 29; 41(1):106-13. PubMed ID: 16356594
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  • 16. Design and synthesis of novel substituted quinazoline derivatives as antileishmanial agents.
    Agarwal KC, Sharma V, Shakya N, Gupta S.
    Bioorg Med Chem Lett; 2009 Sep 15; 19(18):5474-7. PubMed ID: 19692240
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  • 18. Synthesis and in vitro antileishmanial activity of 5-substituted-2'-deoxyuridine derivatives.
    Peyron C, Benhida R, Bories C, Loiseau PM.
    Bioorg Chem; 2005 Dec 15; 33(6):439-47. PubMed ID: 16168460
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  • 19. Looking for new antileishmanial derivatives in 8-nitroquinolin-2(1H)-one series.
    Kieffer C, Cohen A, Verhaeghe P, Hutter S, Castera-Ducros C, Laget M, Remusat V, M'Rabet MK, Rault S, Rathelot P, Azas N, Vanelle P.
    Eur J Med Chem; 2015 Mar 06; 92():282-94. PubMed ID: 25559208
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  • 20. Eugenol derived immunomodulatory molecules against visceral leishmaniasis.
    Charan Raja MR, Velappan AB, Chellappan D, Debnath J, Kar Mahapatra S.
    Eur J Med Chem; 2017 Oct 20; 139():503-518. PubMed ID: 28826085
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