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Journal Abstract Search

409 related items for PubMed ID: 24789926

  • 1. Synthesis and antimicrobial evaluation of some new 1,2-bis-(2-(N-arylimino)-1,3-thiazolidin-3-yl)ethane derivatives.
    Dawood KM, Abu-Deif HK.
    Chem Pharm Bull (Tokyo); 2014; 62(5):439-45. PubMed ID: 24789926
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of some new 2-(3-pyridyl)-4,5-disubstituted thiazoles as potent antimicrobial agents.
    Bondock S, Naser T, Ammar YA.
    Eur J Med Chem; 2013 Apr; 62():270-9. PubMed ID: 23357308
    [Abstract] [Full Text] [Related]

  • 3. Structural modifications and antimicrobial activity of N-cycloalkenyl-2-acylalkylidene-2,3-dihydro-1,3-benzothiazoles.
    Latrofa A, Franco M, Lopedota A, Rosato A, Carone D, Vitali C.
    Farmaco; 2005 Apr; 60(4):291-7. PubMed ID: 15848203
    [Abstract] [Full Text] [Related]

  • 4. Antimicrobial Activity of New 2-Thioxo-benzo[g]quinazolin-4(3H)-one Derivatives.
    Al-Salahi R, Abuelizz HA, Dib RE, Marzouk M, Alshammari MB.
    Med Chem; 2016 Apr; 13(1):85-92. PubMed ID: 27306606
    [Abstract] [Full Text] [Related]

  • 5. Design and total synthesis of (-)-codonopsinine, (-)-codonopsine and codonopsinine analogues by O-(2-oxopyrrolidin-5-yl)trichloroacetimidate as amidoalkylating agent with improved antimicrobial activity via solid lipid nanoparticle formulations.
    El-Nezhawy AOH, Alrobaian M, Khames A, El-Badawy MF, Abdelwahab SF.
    Bioorg Med Chem; 2019 Apr 01; 27(7):1263-1273. PubMed ID: 30777662
    [Abstract] [Full Text] [Related]

  • 6. Synthesis of Mannich bases of some 2,5-disubstituted 4-thiazolidinones and evaluation of their antimicrobial activities.
    Kocabalkanli A, Ates O, Otük G.
    Arch Pharm (Weinheim); 2001 Feb 01; 334(2):35-9. PubMed ID: 11268772
    [Abstract] [Full Text] [Related]

  • 7. Hydrazonoyl bromide precursors as DHFR inhibitors for the synthesis of bis-thiazolyl pyrazole derivatives; antimicrobial activities, antibiofilm, and drug combination studies against MRSA.
    Ibrahim SA, Fayed EA, Rizk HF, Desouky SE, Ragab A.
    Bioorg Chem; 2021 Nov 01; 116():105339. PubMed ID: 34530234
    [Abstract] [Full Text] [Related]

  • 8. Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring.
    Bharti SK, Nath G, Tilak R, Singh SK.
    Eur J Med Chem; 2010 Feb 01; 45(2):651-60. PubMed ID: 19932927
    [Abstract] [Full Text] [Related]

  • 9. Design, synthesis and antimicrobial properties of novel 3,3a,4,5,6,7- hexahydroindazole and arylthiazolylpyrazoline derivatives.
    Bishnoi A, Singh S, Tiwari AK, Sethi A, Tripathi CM.
    Med Chem; 2013 Feb 01; 9(1):45-52. PubMed ID: 22779793
    [Abstract] [Full Text] [Related]

  • 10. Synthesis and in vitro antimicrobial activity of novel N-(6-chlorobenzo[d]thiazol-2-yl) hydrazine carboxamide derivatives of benzothiazole class.
    Gilani SJ, Khan SA, Siddiqui N, Verma SP, Mullick P, Alam O.
    J Enzyme Inhib Med Chem; 2011 Jun 01; 26(3):332-40. PubMed ID: 20807086
    [Abstract] [Full Text] [Related]

  • 11. Synthesis and biological evaluation of some 2,4,5-trisubstituted thiazole derivatives as potential antimicrobial and anticancer agents.
    Al-Saadi MS, Faidallah HM, Rostom SA.
    Arch Pharm (Weinheim); 2008 Jul 01; 341(7):424-34. PubMed ID: 18574850
    [Abstract] [Full Text] [Related]

  • 12. Regioselective synthesis and antimicrobial activities of some novel aryloxyacetic acid derivatives.
    Abdel-Wahab BF, Khidre RE, Awad GE.
    Eur J Med Chem; 2012 Apr 01; 50():55-62. PubMed ID: 22373733
    [Abstract] [Full Text] [Related]

  • 13. Synthesis, antimicrobial activity and acid dissociation constants of methyl 5,5-diphenyl-1-(thiazol-2-yl)pyrrolidine-2-carboxylate derivatives.
    Nural Y, Gemili M, Ulger M, Sari H, De Coen LM, Sahin E.
    Bioorg Med Chem Lett; 2018 Mar 01; 28(5):942-946. PubMed ID: 29433925
    [Abstract] [Full Text] [Related]

  • 14. Design, synthesis and antimicrobial evaluation of novel 1,3-oxazolidin-2- one derivatives.
    Chandna N, Kapoor JK, Goyal V, Aggarwal NK, Kumari KM, Vijjulatha M.
    Curr Top Med Chem; 2013 Aug 01; 13(16):2062-75. PubMed ID: 23895090
    [Abstract] [Full Text] [Related]

  • 15. Antimicrobial study of newly synthesized 6-substituted indolo[1,2-c]quinazolines.
    Rohini R, Muralidhar Reddy P, Shanker K, Hu A, Ravinder V.
    Eur J Med Chem; 2010 Mar 01; 45(3):1200-5. PubMed ID: 20005020
    [Abstract] [Full Text] [Related]

  • 16. Novel indole-thiazolidinone conjugates: Design, synthesis and whole-cell phenotypic evaluation as a novel class of antimicrobial agents.
    Abo-Ashour MF, Eldehna WM, George RF, Abdel-Aziz MM, Elaasser MM, Abdel Gawad NM, Gupta A, Bhakta S, Abou-Seri SM.
    Eur J Med Chem; 2018 Dec 05; 160():49-60. PubMed ID: 30317025
    [Abstract] [Full Text] [Related]

  • 17. Design and synthesis of spiro[indole-thiazolidine]spiro[indole-pyrans] as antimicrobial agents.
    Sakhuja R, Panda SS, Khanna L, Khurana S, Jain SC.
    Bioorg Med Chem Lett; 2011 Sep 15; 21(18):5465-9. PubMed ID: 21782421
    [Abstract] [Full Text] [Related]

  • 18. Studies on heterocyclic compounds: spiro [indole-3,2'-thiazolidine] derivatives. II. Antimicrobial activity of halogenated 3'-phenylspiro 3H-indole-3,2'-thiazolidine -2,4 (1H)-diones.
    Piscopo E, Diurno MV, Mazzoni O, Ciaccio AM, Veneruso G.
    Boll Soc Ital Biol Sper; 1990 Dec 15; 66(12):1187-91. PubMed ID: 2100531
    [Abstract] [Full Text] [Related]

  • 19. Studies on heterocyclic compounds: spiro [indole-3,2'-thiazolidine] derivatives. Antimicrobial activity of monohalogenated 3'-phenylspiro 3H-indole-3,2'-thiazolidine-2,4' (1H)-diones.
    Piscopo E, Diurno MV, Mazzoni O, Ciaccio AM.
    Boll Soc Ital Biol Sper; 1990 Dec 15; 66(12):1181-6. PubMed ID: 2100530
    [Abstract] [Full Text] [Related]

  • 20. Synthesis and biological evaluation of a new series of N-acyldiamines as potential antibacterial and antifungal agents.
    Ferreira BDS, de Almeida AM, Nascimento TC, de Castro PP, Silva VL, Diniz CG, Le Hyaric M.
    Bioorg Med Chem Lett; 2014 Oct 01; 24(19):4626-4629. PubMed ID: 25219900
    [Abstract] [Full Text] [Related]

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