These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
156 related articles for article (PubMed ID: 20022500)
1. Synthesis and antituberculosis activity of novel mefloquine-isoxazole carboxylic esters as prodrugs. Mao J; Yuan H; Wang Y; Wan B; Pak D; He R; Franzblau SG Bioorg Med Chem Lett; 2010 Feb; 20(3):1263-8. PubMed ID: 20022500 [TBL] [Abstract][Full Text] [Related]
2. From serendipity to rational antituberculosis drug discovery of mefloquine-isoxazole carboxylic acid esters. Mao J; Yuan H; Wang Y; Wan B; Pieroni M; Huang Q; van Breemen RB; Kozikowski AP; Franzblau SG J Med Chem; 2009 Nov; 52(22):6966-78. PubMed ID: 19863050 [TBL] [Abstract][Full Text] [Related]
3. Rational design of 5-phenyl-3-isoxazolecarboxylic acid ethyl esters as growth inhibitors of Mycobacterium tuberculosis. a potent and selective series for further drug development. Lilienkampf A; Pieroni M; Wan B; Wang Y; Franzblau SG; Kozikowski AP J Med Chem; 2010 Jan; 53(2):678-88. PubMed ID: 20000577 [TBL] [Abstract][Full Text] [Related]
4. Design, synthesis, and pharmacological evaluation of mefloquine-based ligands as novel antituberculosis agents. Mao J; Wang Y; Wan B; Kozikowski AP; Franzblau SG ChemMedChem; 2007 Nov; 2(11):1624-30. PubMed ID: 17680579 [TBL] [Abstract][Full Text] [Related]
5. Antitubercular activities of novel benzothiazolo naphthyridone carboxylic acid derivatives endowed with high activity toward multi-drug resistant tuberculosis. Dinakaran M; Senthilkumar P; Yogeeswari P; Sriram D Biomed Pharmacother; 2009 Jan; 63(1):11-8. PubMed ID: 18078735 [TBL] [Abstract][Full Text] [Related]
6. Structure-activity relationships for a series of quinoline-based compounds active against replicating and nonreplicating Mycobacterium tuberculosis. Lilienkampf A; Mao J; Wan B; Wang Y; Franzblau SG; Kozikowski AP J Med Chem; 2009 Apr; 52(7):2109-18. PubMed ID: 19271749 [TBL] [Abstract][Full Text] [Related]
7. Synthesis, biological evaluation, and structure-activity relationships for 5-[(E)-2-arylethenyl]-3-isoxazolecarboxylic acid alkyl ester derivatives as valuable antitubercular chemotypes. Pieroni M; Lilienkampf A; Wan B; Wang Y; Franzblau SG; Kozikowski AP J Med Chem; 2009 Oct; 52(20):6287-96. PubMed ID: 19757815 [TBL] [Abstract][Full Text] [Related]
8. A prodrug approach for improving antituberculosis activity of potent Mycobacterium tuberculosis type II dehydroquinase inhibitors. Tizón L; Otero JM; Prazeres VF; Llamas-Saiz AL; Fox GC; van Raaij MJ; Lamb H; Hawkins AR; Ainsa JA; Castedo L; González-Bello C J Med Chem; 2011 Sep; 54(17):6063-84. PubMed ID: 21780742 [TBL] [Abstract][Full Text] [Related]
9. Synthesis and antituberculosis activity of a novel series of optically active 6-nitro-2,3-dihydroimidazo[2,1-b]oxazoles. Sasaki H; Haraguchi Y; Itotani M; Kuroda H; Hashizume H; Tomishige T; Kawasaki M; Matsumoto M; Komatsu M; Tsubouchi H J Med Chem; 2006 Dec; 49(26):7854-60. PubMed ID: 17181168 [TBL] [Abstract][Full Text] [Related]
10. Synthesis, anti-HIV and antitubercular activities of lamivudine prodrugs. Sriram D; Yogeeswari P; Gopal G Eur J Med Chem; 2005 Dec; 40(12):1373-6. PubMed ID: 16129516 [TBL] [Abstract][Full Text] [Related]
11. Isoxazole analogs of curcuminoids with highly potent multidrug-resistant antimycobacterial activity. Changtam C; Hongmanee P; Suksamrarn A Eur J Med Chem; 2010 Oct; 45(10):4446-57. PubMed ID: 20691508 [TBL] [Abstract][Full Text] [Related]
12. Lipophilic pyrazinoic acid amide and ester prodrugs stability, activation and activity against M. tuberculosis. Simões MF; Valente E; Gómez MJ; Anes E; Constantino L Eur J Pharm Sci; 2009 Jun; 37(3-4):257-63. PubMed ID: 19491013 [TBL] [Abstract][Full Text] [Related]
13. Searching for new cures for tuberculosis: design, synthesis, and biological evaluation of 2-methylbenzothiazoles. Huang Q; Mao J; Wan B; Wang Y; Brun R; Franzblau SG; Kozikowski AP J Med Chem; 2009 Nov; 52(21):6757-67. PubMed ID: 19817445 [TBL] [Abstract][Full Text] [Related]
14. Synthesis and Antibacterial Activity of Mefloquine-Based Analogs Against Sensitive and Resistant Mycobacterium tuberculosis Strains. da Silva Araújo A; Moraes AM; Lourenço MCS; Pessoa CO; da Silva ET; de Souza MVN Curr Top Med Chem; 2019; 19(9):683-689. PubMed ID: 30836914 [TBL] [Abstract][Full Text] [Related]
15. Synthesis of novel [1,2]-diamines with antituberculosis activity. Meng Q; Luo H; Chen Y; Wang T; Yao Q Bioorg Med Chem Lett; 2009 Sep; 19(18):5372-5. PubMed ID: 19682895 [TBL] [Abstract][Full Text] [Related]
16. Derivatives of 3-isoxazolecarboxylic acid esters: a potent and selective compound class against replicating and nonreplicating Mycobacterium tuberculosis. Lilienkampf A; Pieroni M; Franzblau SG; Bishai WR; Kozikowski AP Curr Top Med Chem; 2012; 12(7):729-34. PubMed ID: 22283815 [TBL] [Abstract][Full Text] [Related]
17. Synthesis and antitubercular activity of new mefloquine-oxazolidine derivatives. Gonçalves RS; Kaiser CR; Lourenço MC; de Souza MV; Wardell JL; Wardell SM; da Silva AD Eur J Med Chem; 2010 Dec; 45(12):6095-100. PubMed ID: 20932608 [TBL] [Abstract][Full Text] [Related]
18. Antimycobacterial activity of pyrazinoate prodrugs in replicating and non-replicating Mycobacterium tuberculosis. Segretti ND; Simões CK; Corrêa MF; Felli VMA; Miyata M; Cho SH; Franzblau SG; Fernandes JPDS Tuberculosis (Edinb); 2016 Jul; 99():11-16. PubMed ID: 27449999 [TBL] [Abstract][Full Text] [Related]
19. Synthesis and in vitro antitubercular activity of some 1-[(4-sub)phenyl]-3-(4-{1-[(pyridine-4-carbonyl)hydrazono]ethyl}phenyl)thiourea. Sriram D; Yogeeswari P; Madhu K Bioorg Med Chem Lett; 2006 Feb; 16(4):876-8. PubMed ID: 16303302 [TBL] [Abstract][Full Text] [Related]
20. Synthesis of isonicotinic acid N'-arylidene-N-[2-oxo-2-(4-aryl-piperazin-1-yl)-ethyl]-hydrazides as antituberculosis agents. Sinha N; Jain S; Tilekar A; Upadhayaya RS; Kishore N; Jana GH; Arora SK Bioorg Med Chem Lett; 2005 Mar; 15(6):1573-6. PubMed ID: 15745799 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]