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Journal Abstract Search

251 related items for PubMed ID: 10915058

  • 1. Synthesis and antifungal activities of 5/6-arylamino-4,7-dioxobenzothiazoles.
    Ryu CK, Kang HY, Yi YJ, Shin KH, Lee BH.
    Bioorg Med Chem Lett; 2000 Jul 17; 10(14):1589-91. PubMed ID: 10915058
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  • 2. Synthesis and antifungal activity of 6-arylthio-/6-arylamino-4,7-dioxobenzothiazoles.
    Ryu CK, Choi KU, Shim JY, You HJ, Choi IH, Chae MJ.
    Bioorg Med Chem; 2003 Sep 01; 11(18):4003-8. PubMed ID: 12927862
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  • 3. Synthesis and antifungal activity of 2,5-disubstituted-6-arylamino-4,7-benzimidazolediones.
    -Ryu CK, Song EH, Shim JY, You HJ, Choi KU, Choi IH, Lee EY, Chae MJ.
    Bioorg Med Chem Lett; 2003 Jan 06; 13(1):17-20. PubMed ID: 12467608
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  • 4. Synthesis and antifungal activity of naphthalene-1,4-diones modified at positions 2, 3, and 5.
    Ryu CK, Chae MJ.
    Arch Pharm Res; 2005 Jul 06; 28(7):750-5. PubMed ID: 16114486
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  • 5. Synthesis and antifungal activity of 5,8-quinazolinedione derivatives modified at positions 6 and 7.
    Ryu CK, Shim JY, Yi YJ, Choi IH, Chae MJ, Han JY, Jung OJ.
    Arch Pharm Res; 2004 Oct 06; 27(10):990-6. PubMed ID: 15554252
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  • 6. Synthesis and antimicrobial evaluation of novel ethyl 2-(2-(4-substituted)acetamido)-4-subtituted-thiazole-5-carboxylate derivatives.
    Pawar CD, Sarkate AP, Karnik KS, Bahekar SS, Pansare DN, Shelke RN, Jawale CS, Shinde DB.
    Bioorg Med Chem Lett; 2016 Aug 01; 26(15):3525-8. PubMed ID: 27324976
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  • 11. Synthesis of potent and selective inhibitors of Candida albicans N-myristoyltransferase based on the benzothiazole structure.
    Yamazaki K, Kaneko Y, Suwa K, Ebara S, Nakazawa K, Yasuno K.
    Bioorg Med Chem; 2005 Apr 01; 13(7):2509-22. PubMed ID: 15755653
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  • 13. Synthesis and antifungal evaluation of 7-arylamino-5,8-dioxo-5,8-dihydroisoquinoline-4-carboxylates.
    Ryu CK, Song AL, Hong JA.
    Bioorg Med Chem Lett; 2013 Apr 01; 23(7):2065-8. PubMed ID: 23453842
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  • 14. Total synthesis and further scrutiny of the in vitro antifungal activity of 6-nonadecynoic acid.
    Carballeira NM, Sanabria D, Parang K.
    Arch Pharm (Weinheim); 2005 Sep 01; 338(9):441-3. PubMed ID: 16143955
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  • 17. Synthesis and cytotoxicity of novel (thiazol-2-yl)hydrazine derivatives as promising anti-Candida agents.
    Carradori S, Secci D, Bolasco A, Rivanera D, Mari E, Zicari A, Lotti LV, Bizzarri B.
    Eur J Med Chem; 2013 Jul 01; 65():102-11. PubMed ID: 23702472
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  • 18. Stereoselective synthesis and in vitro antifungal evaluation of (E)- and (Z)-imidazolylchromanone oxime ethers.
    Emami S, Falahati M, Banifatemi A, Moshiri K, Shafiee A.
    Arch Pharm (Weinheim); 2002 Jul 01; 335(7):318-24. PubMed ID: 12207281
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  • 19. Synthesis, antimicrobial and cytotoxicity study of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines.
    Verma V, Singh K, Kumar D, Klapötke TM, Stierstorfer J, Narasimhan B, Qazi AK, Hamid A, Jaglan S.
    Eur J Med Chem; 2012 Oct 01; 56():195-202. PubMed ID: 22982123
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  • 20. Synthesis and biological evaluation of novel 2,4-disubstituted-1,3-thiazoles as anti-Candida spp. agents.
    Chimenti F, Bizzarri B, Bolasco A, Secci D, Chimenti P, Granese A, Carradori S, D'Ascenzio M, Lilli D, Rivanera D.
    Eur J Med Chem; 2011 Jan 01; 46(1):378-82. PubMed ID: 21084135
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