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: 29525348)
21. Discovery of mixed type thymidine phosphorylase inhibitors endowed with antiangiogenic properties: synthesis, pharmacological evaluation and molecular docking study of 2-thioxo-pyrazolo[1,5-a][1,3,5]triazin-4-ones. Part II. Bera H; Ojha Pk; Tan BJ; Sun L; Dolzhenko AV; Chui WK; Chiu GN Eur J Med Chem; 2014 May; 78():294-303. PubMed ID: 24686016 [TBL] [Abstract][Full Text] [Related]
22. A structure-activity relationship study of 1,2,4-triazolo[1,5-a][1,3,5]triazin-5,7-dione and its 5-thioxo analogues on anti-thymidine phosphorylase and associated anti-angiogenic activities. Bera H; Tan BJ; Sun L; Dolzhenko AV; Chui WK; Chiu GN Eur J Med Chem; 2013 Sep; 67():325-34. PubMed ID: 23871912 [TBL] [Abstract][Full Text] [Related]
23. Design, synthesis, modelling studies and biological evaluation of 1,3,4-oxadiazole derivatives as potent anticancer agents targeting thymidine phosphorylase enzyme. Bajaj S; Kumar MS; Tinwala H; Yc M Bioorg Chem; 2021 Jun; 111():104873. PubMed ID: 33845381 [TBL] [Abstract][Full Text] [Related]
24. Synthesis, thymidine phosphorylase inhibitory and computational study of novel 1,3,4-oxadiazole-2-thione derivatives as potential anticancer agents. Bajaj S; Roy PP; Singh J Comput Biol Chem; 2018 Oct; 76():151-160. PubMed ID: 30015176 [TBL] [Abstract][Full Text] [Related]
25. Synthesis and biological evaluation of indole derivatives as α-amylase inhibitor. Imran S; Taha M; Selvaraj M; Ismail NH; Chigurupati S; Mohammad JI Bioorg Chem; 2017 Aug; 73():121-127. PubMed ID: 28648924 [TBL] [Abstract][Full Text] [Related]
26. Schiff bases of 3-formylchromone as thymidine phosphorylase inhibitors. Khan KM; Ambreen N; Hussain S; Perveen S; Choudhary MI Bioorg Med Chem; 2009 Apr; 17(8):2983-8. PubMed ID: 19329330 [TBL] [Abstract][Full Text] [Related]
27. Facile benzothiazole-triazole based thiazole derivatives as novel thymidine phosphorylase and α-glucosidase inhibitors: Experimental and computational approaches. Khan S; Hussain R; Khan Y; Iqbal T; Ullah F; Felemban S; Khowdiary MM Enzyme Microb Technol; 2024 Sep; 179():110470. PubMed ID: 38917733 [TBL] [Abstract][Full Text] [Related]
28. Synthesis and biological evaluation of novel oxadiazole derivatives: a new class of thymidine phosphorylase inhibitors as potential anti-tumor agents. Shahzad SA; Yar M; Bajda M; Jadoon B; Khan ZA; Naqvi SA; Shaikh AJ; Hayat K; Mahmmod A; Mahmood N; Filipek S Bioorg Med Chem; 2014 Feb; 22(3):1008-15. PubMed ID: 24411198 [TBL] [Abstract][Full Text] [Related]
29. Synthesis and evaluation of 6-methylene-bridged uracil derivatives. Part 2: optimization of inhibitors of human thymidine phosphorylase and their selectivity with uridine phosphorylase. Yano S; Kazuno H; Sato T; Suzuki N; Emura T; Wierzba K; Yamashita J; Tada Y; Yamada Y; Fukushima M; Asao T Bioorg Med Chem; 2004 Jul; 12(13):3443-50. PubMed ID: 15186830 [TBL] [Abstract][Full Text] [Related]
30. Natural compounds as angiogenic enzyme thymidine phosphorylase inhibitors: In vitro biochemical inhibition, mechanistic, and in silico modeling studies. Javaid S; Shaikh M; Fatima N; Choudhary MI PLoS One; 2019; 14(11):e0225056. PubMed ID: 31743355 [TBL] [Abstract][Full Text] [Related]
31. Synthesis and evaluation of multisubstrate bicyclic pyrimidine nucleoside inhibitors of human thymidine phosphorylase. Allan AL; Gladstone PL; Price ML; Hopkins SA; Juarez JC; Doñate F; Ternansky RJ; Shaw DE; Ganem B; Li Y; Wang W; Ealick S J Med Chem; 2006 Dec; 49(26):7807-15. PubMed ID: 17181163 [TBL] [Abstract][Full Text] [Related]
32. Rational design of bis-indolylmethane-oxadiazole hybrids as inhibitors of thymidine phosphorylase. Taha M; Rashid U; Imran S; Ali M Bioorg Med Chem; 2018 Jul; 26(12):3654-3663. PubMed ID: 29853339 [TBL] [Abstract][Full Text] [Related]
33. Design and synthesis of novel 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase. Nencka R; Votruba I; Hrebabecký H; Tloust'ová E; Horská K; Masojídková M; Holý A Bioorg Med Chem Lett; 2006 Mar; 16(5):1335-7. PubMed ID: 16337119 [TBL] [Abstract][Full Text] [Related]
34. Thymidine phosphorylase and prostrate cancer cell proliferation inhibitory activities of synthetic 4-hydroxybenzohydrazides: In vitro, kinetic, and in silico studies. Javaid S; Saad SM; Zafar H; Malik R; Khan KM; Choudhary MI; Rahman AU PLoS One; 2020; 15(1):e0227549. PubMed ID: 31986186 [TBL] [Abstract][Full Text] [Related]
36. Design, synthesis and enzymatic evaluation of 6-bridged imidazolyluracil derivatives as inhibitors of human thymidine phosphorylase. McNally VA; Rajabi M; Gbaj A; Stratford IJ; Edwards PN; Douglas KT; Bryce RA; Jaffar M; Freeman S J Pharm Pharmacol; 2007 Apr; 59(4):537-47. PubMed ID: 17430637 [TBL] [Abstract][Full Text] [Related]
37. Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies. Taha M; Ismail NH; Imran S; Wadood A; Rahim F; Khan KM; Riaz M Bioorg Chem; 2016 Jun; 66():80-7. PubMed ID: 27038849 [TBL] [Abstract][Full Text] [Related]
38. Fragment-based approach to the design of 5-chlorouracil-linked-pyrazolo[1,5-a][1,3,5]triazines as thymidine phosphorylase inhibitors. Sun L; Li J; Bera H; Dolzhenko AV; Chiu GN; Chui WK Eur J Med Chem; 2013; 70():400-10. PubMed ID: 24177367 [TBL] [Abstract][Full Text] [Related]
39. Synthesis and evaluation of 6-methylene-bridged uracil derivatives. Part 1: discovery of novel orally active inhibitors of human thymidine phosphorylase. Yano S; Kazuno H; Suzuki N; Emura T; Wierzba K; Yamashita J; Tada Y; Yamada Y; Fukushima M; Asao T Bioorg Med Chem; 2004 Jul; 12(13):3431-41. PubMed ID: 15186829 [TBL] [Abstract][Full Text] [Related]
40. Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives. Taha M; Tariq Javid M; Imran S; Selvaraj M; Chigurupati S; Ullah H; Rahim F; Khan F; Islam Mohammad J; Mohammed Khan K Bioorg Chem; 2017 Oct; 74():179-186. PubMed ID: 28826047 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]