BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 33396536)

  • 1. Antibacterial Activity of Fluorobenzoylthiosemicarbazides and Their Cyclic Analogues with 1,2,4-Triazole Scaffold.
    Kosikowska U; Wujec M; Trotsko N; Płonka W; Paneth P; Paneth A
    Molecules; 2020 Dec; 26(1):. PubMed ID: 33396536
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and antimicrobial activity of thiosemicarbazides, s-triazoles and their Mannich bases bearing 3-chlorophenyl moiety.
    Plech T; Wujec M; Siwek A; Kosikowska U; Malm A
    Eur J Med Chem; 2011 Jan; 46(1):241-8. PubMed ID: 21130541
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New thiophene-1,2,4-triazole-5(3)-ones: highly bioactive thiosemicarbazides, structures of Schiff bases and triazole-thiols.
    Ünver Y; Sancak K; Çelik F; Birinci E; Küçük M; Soylu S; Burnaz NA
    Eur J Med Chem; 2014 Sep; 84():639-50. PubMed ID: 25063946
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis of 1,2,3-triazole linked 4(3H)-Quinazolinones as potent antibacterial agents against multidrug-resistant Staphylococcus aureus.
    Gatadi S; Gour J; Shukla M; Kaul G; Das S; Dasgupta A; Malasala S; Borra RS; Madhavi YV; Chopra S; Nanduri S
    Eur J Med Chem; 2018 Sep; 157():1056-1067. PubMed ID: 30176536
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 1-(2-Hydroxybenzoyl)-thiosemicarbazides are promising antimicrobial agents targeting d-alanine-d-alanine ligase in bacterio.
    Ameryckx A; Thabault L; Pochet L; Leimanis S; Poupaert JH; Wouters J; Joris B; Van Bambeke F; Frédérick R
    Eur J Med Chem; 2018 Nov; 159():324-338. PubMed ID: 30300845
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synergistic Effects of Thiosemicarbazides with Clinical Drugs against
    Chudzik-Rząd B; Malm A; Trotsko N; Wujec M; Plech T; Paneth A
    Molecules; 2020 May; 25(10):. PubMed ID: 32422899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis and structure-activity relationship studies of 4-arylthiosemicarbazides as topoisomerase IV inhibitors with Gram-positive antibacterial activity. Search for molecular basis of antibacterial activity of thiosemicarbazides.
    Siwek A; Stączek P; Stefańska J
    Eur J Med Chem; 2011 Nov; 46(11):5717-26. PubMed ID: 21978836
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The relationship between structure and in vitro antibacterial activity of selected isoflavones and their metabolites with special focus on antistaphylococcal effect of demethyltexasin.
    Hummelova J; Rondevaldova J; Balastikova A; Lapcik O; Kokoska L
    Lett Appl Microbiol; 2015 Mar; 60(3):242-7. PubMed ID: 25421722
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis and in Vitro Antibacterial Evaluation of Novel 4-Substituted 1-Menthyl-1,2,3-triazoles.
    Khaligh P; Salehi P; Bararjanian M; Aliahmadi A; Khavasi HR; Nejad-Ebrahimi S
    Chem Pharm Bull (Tokyo); 2016; 64(11):1589-1596. PubMed ID: 27803470
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structure-activity relationships of some 4-quinazolylthiosemicarbazides and their triazolo derivatives.
    Jantová S; Hudecová D; Spirková K; Stankovský S
    Folia Microbiol (Praha); 1994; 39(6):471-4. PubMed ID: 8549994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Antibacterial Activity of 1,2,3-triazole- and 1,2,4-Triazole-containing Hybrids against
    Li J; Zhang J
    Curr Top Med Chem; 2022; 22(1):41-63. PubMed ID: 34766892
    [No Abstract]   [Full Text] [Related]  

  • 12. Design, synthesis and biological evaluation of 4-benzoyl-1-dichlorobenzoylthiosemicarbazides as potent Gram-positive antibacterial agents.
    Paneth A; Plech T; Kaproń B; Hagel D; Kosikowska U; Kuśmierz E; Dzitko K; Paneth P
    J Enzyme Inhib Med Chem; 2016; 31(3):434-40. PubMed ID: 25897586
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Design, synthesis and antibacterial activities of 5-(pyrazin-2-yl)-4H-1,2,4-triazole-3-thiol derivatives containing Schiff base formation as FabH inhibitory.
    Zhang F; Wen Q; Wang SF; Shahla Karim B; Yang YS; Liu JJ; Zhang WM; Zhu HL
    Bioorg Med Chem Lett; 2014 Jan; 24(1):90-5. PubMed ID: 24332628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A New 1,2,3-Triazole Scaffold with Improved Potency against
    Stachura DL; Nguyen S; Polyak SW; Jovcevski B; Bruning JB; Abell AD
    ACS Infect Dis; 2022 Dec; 8(12):2579-2585. PubMed ID: 36399035
    [No Abstract]   [Full Text] [Related]  

  • 15. Thiosemicarbazide Derivatives Decrease the ATPase Activity of
    Kowalczyk A; Paneth A; Trojanowski D; Paneth P; Zakrzewska-Czerwińska J; Stączek P
    Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33918623
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Efficient synthesis and antimicrobial activity of some novel S-β-d-glucosides of 5-aryl-1,2,4-triazole-3-thiones derivatives.
    Ji D; Lu J; Lu B; Xin C; Mu J; Li J; Peng C; Bao X
    Bioorg Med Chem Lett; 2013 Apr; 23(7):1997-2000. PubMed ID: 23466234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cleistochlamys kirkii chemical constituents: Antibacterial activity and synergistic effects against resistant Staphylococcus aureus strains.
    Pereira F; Madureira AM; Sancha S; Mulhovo S; Luo X; Duarte A; Ferreira MJ
    J Ethnopharmacol; 2016 Feb; 178():180-7. PubMed ID: 26674158
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Design, synthesis and antibacterial evaluation of novel 15-membered 11a-azahomoclarithromycin derivatives with the 1, 2, 3-triazole side chain.
    Qin Y; Teng Y; Ma R; Bi F; Liu Z; Zhang P; Ma S
    Eur J Med Chem; 2019 Oct; 180():321-339. PubMed ID: 31323617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Design, synthesis, biological activities and DFT calculation of novel 1,2,4-triazole Schiff base derivatives.
    Jin RY; Zeng CY; Liang XH; Sun XH; Liu YF; Wang YY; Zhou S
    Bioorg Chem; 2018 Oct; 80():253-260. PubMed ID: 29966871
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA).
    Xu Z
    Eur J Med Chem; 2020 Nov; 206():112686. PubMed ID: 32795773
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.