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Journal Abstract Search

219 related items for PubMed ID: 12641321

  • 1.
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  • 2. Relationships between the chemical structure of antimycobacterial substances and their activity against atypical strains. Part 14: 3-Aryl-6,8-dihalogeno-2H-1,3-benzoxazine-2,4(3H)-diones.
    Waisser K, Hladuvková J, Gregor J, Rada T, Kubicová L, Klimesová V, Kaustová J.
    Arch Pharm (Weinheim); 1998 Jan; 331(1):3-6. PubMed ID: 9507695
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  • 3. New groups of antimycobacterial agents: 6-chloro-3-phenyl-4-thioxo-2H-1,3-benzoxazine-2(3H)-ones and 6-chloro-3-phenyl-2H-1,3-benzoxazine-2,4(3H)-dithiones.
    Waisser K, Gregor J, Kubicová L, Klimesová V, Kunes J, Machácek M, Kaustová J.
    Eur J Med Chem; 2000 Jan; 35(7-8):733-41. PubMed ID: 10960190
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  • 4. Influence of the replacement of the oxo function with the thioxo group on the antimycobacterial activity of 3-aryl-6,8-dichloro-2H-1,3-benzoxazine-2,4(3H)-diones and 3-arylquinazoline-2,4(1H,3H)-diones.
    Waisser K, Gregor J, Dostál H, Kunes J, Kubicová L, Klimesová V, Kaustová J.
    Farmaco; 2001 Oct; 56(10):803-7. PubMed ID: 11718275
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  • 5. [Antimicrobial salicylanilides and 3-phenyl-2H-1,3-benzoxazine-2,4(3H)-diones].
    Waisser K, Gregor J, Holý P, Kubicová L, Klimesová V, Kaustová J.
    Ceska Slov Farm; 2001 May; 50(3):148-52. PubMed ID: 11394023
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  • 6. 3-Benzyl-2H-1,3-benzoxazine-2,4(3H)-diones, a new group of antimycobacterial compounds against potentially pathogenic strains.
    Waisser K, Perina M, Kunes J, Klimesová V, Kaustová J.
    Farmaco; 2003 Nov; 58(11):1137-49. PubMed ID: 14572865
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  • 10. Highly active potential antituberculotics: 3-(4-alkylphenyl)-4-thioxo-2H-1,3-benzoxazine-2(3H)-ones and 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-dihiones substituted in ring-B by halogen.
    Waisser K, Matyk J, Kunes J, Dolezal R, Kaustová J, Dahse HM.
    Arch Pharm (Weinheim); 2008 Dec; 341(12):800-3. PubMed ID: 19006090
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  • 11. Highly active antimycobacterial derivatives of benzoxazine.
    Petrlíková E, Waisser K, Divišová H, Husáková P, Vrabcová P, Kuneš J, Kolář K, Stolaříková J.
    Bioorg Med Chem; 2010 Dec 01; 18(23):8178-87. PubMed ID: 21044844
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  • 12. A note to the biological activity of benzoxazine derivatives containing the thioxo group.
    Waisser K, Petrlíková E, Perina M, Klimesová V, Kunes J, Palát K, Kaustová J, Dahse HM, Möllmann U.
    Eur J Med Chem; 2010 Jul 01; 45(7):2719-25. PubMed ID: 20226572
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  • 15. Antimycobacterial activity of 5-arylidene derivatives of hydantoin.
    Kieć-Kononowicz K, Szymańska E.
    Farmaco; 2002 Nov 01; 57(11):909-16. PubMed ID: 12484539
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  • 16. Synthesis and antimycobacterial activity of pyridylmethylsulfanyl and naphthylmethylsulfanyl derivatives of benzazoles, 1, 2, 4-triazole, and pyridine-2-carbothioamide/-2-carbonitrile.
    Zahajská L, Klimesová V, Kocí J, Waisser K, Kaustová J.
    Arch Pharm (Weinheim); 2004 Oct 01; 337(10):549-55. PubMed ID: 15476287
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  • 17. Synthesis of some 2,6-bis(alkylthio)-4-pyridine carboxamides and carboxthioamides and their antimycobacterial and antialgal activity.
    Miletín M, Hartl J, Odlerová Z, Machácek M.
    Pharmazie; 1997 Jul 01; 52(7):558-60. PubMed ID: 9266594
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  • 19. Similarity approach to QSAR. Application to antimycobacterial benzoxazines.
    Gallegos A, Carbó-Dorca R, Ponec R, Waisser K.
    Int J Pharm; 2004 Jan 09; 269(1):51-60. PubMed ID: 14698576
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  • 20. Antimycobacterial N-pyridinylsalicylamides, isosters of salicylamides.
    Waisser K, Drazková K, Kunes J, Klimesová V, Kaustová J.
    Farmaco; 2004 Aug 09; 59(8):615-25. PubMed ID: 15262531
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