108 related articles for article (PubMed ID: 25462623)
1. Synthesis and biological evaluation of 5'-glycyl derivatives of uridine as inhibitors of 1,4-β-galactosyltransferase.
Paszkowska J; Kral K; Bieg T; Żaba K; Węgrzyk K; Jaśkowiak N; Molinaro A; Silipo A; Wandzik I
Bioorg Chem; 2015 Feb; 58():18-25. PubMed ID: 25462623
[TBL] [Abstract][Full Text] [Related]
2. Uncharged nucleoside inhibitors of β-1,4-galactosyltransferase with activity in cells.
Jiang J; Kanabar V; Padilla B; Man F; Pitchford SC; Page CP; Wagner GK
Chem Commun (Camb); 2016 Mar; 52(20):3955-8. PubMed ID: 26882174
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and Preliminary Evaluation of Biological Activity of Glycoconjugates Analogues of Acyclic Uridine Derivatives.
Komor R; Pastuch-Gawolek G; Krol E; Szeja W
Molecules; 2018 Aug; 23(8):. PubMed ID: 30104510
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of 2-deoxy-hexopyranosyl derivatives of uridine as donor substrate analogues for glycosyltransferases.
Wandzik I; Bieg T; Czaplicka M
Bioorg Chem; 2009 Dec; 37(6):211-6. PubMed ID: 19765794
[TBL] [Abstract][Full Text] [Related]
5. Synthesis and preliminary biological assay of uridine glycoconjugate derivatives containing amide and/or 1,2,3-triazole linkers.
Pastuch-Gawolek G; Plesniak M; Komor R; Byczek-Wyrostek A; Erfurt K; Szeja W
Bioorg Chem; 2017 Jun; 72():80-88. PubMed ID: 28384485
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and preliminary biological evaluations of 5'-substituted derivatives of uridine as glycosyltransferase inhibitors.
Paszkowska J; Kral K; Bieg T; Nawrot U; Szeja W; Wandzik I
Molecules; 2013 Jul; 18(7):8018-27. PubMed ID: 23884133
[TBL] [Abstract][Full Text] [Related]
7. Concise syntheses of selective inhibitors against α-1,3-galactosyltransferase.
Zhang GL; Zhang LH; Ye XS
Org Biomol Chem; 2010 Nov; 8(22):5062-8. PubMed ID: 20820649
[TBL] [Abstract][Full Text] [Related]
8. Glycoconjugates, products of uridine derivatives phosphitylation and oxidation as glycosyltransferases potential inhibitors.
Grec M; Swierk P; Pastuch G; Szeja W
Acta Pol Pharm; 2010; 67(6):652-63. PubMed ID: 21229882
[TBL] [Abstract][Full Text] [Related]
9. A new concept for glycosyltransferase inhibitors: nonionic mimics of the nucleotide donor of the human blood group B galactosyltransferase.
Schaefer K; Albers J; Sindhuwinata N; Peters T; Meyer B
Chembiochem; 2012 Feb; 13(3):443-50. PubMed ID: 22223604
[TBL] [Abstract][Full Text] [Related]
10. Rational design, synthesis, and characterization of novel inhibitors for human beta1,4-galactosyltransferase.
Takaya K; Nagahori N; Kurogochi M; Furuike T; Miura N; Monde K; Lee YC; Nishimura S
J Med Chem; 2005 Sep; 48(19):6054-65. PubMed ID: 16162007
[TBL] [Abstract][Full Text] [Related]
11. A nonionic inhibitor with high specificity for the UDP-Gal donor binding site of human blood group B galactosyltransferase: design, synthesis, and characterization.
Schaefer K; Sindhuwinata N; Hackl T; Kötzler MP; Niemeyer FC; Palcic MM; Peters T; Meyer B
J Med Chem; 2013 Mar; 56(5):2150-4. PubMed ID: 23406460
[TBL] [Abstract][Full Text] [Related]
12. Structure-activity relationships of orotidine-5'-monophosphate decarboxylase inhibitors as anticancer agents.
Bello AM; Konforte D; Poduch E; Furlonger C; Wei L; Liu Y; Lewis M; Pai EF; Paige CJ; Kotra LP
J Med Chem; 2009 Mar; 52(6):1648-58. PubMed ID: 19260677
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of isoxazolidine-containing uridine derivatives as caprazamycin analogues.
Yamaguchi M; Matsuda A; Ichikawa S
Org Biomol Chem; 2015 Jan; 13(4):1187-97. PubMed ID: 25428330
[TBL] [Abstract][Full Text] [Related]
14. Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors.
Goeminne A; McNaughton M; Bal G; Surpateanu G; Van Der Veken P; De Prol S; Versées W; Steyaert J; Haemers A; Augustyns K
Eur J Med Chem; 2008 Feb; 43(2):315-26. PubMed ID: 17582660
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases.
Vassiliou S; Grabowiecka A; Kosikowska P; Yiotakis A; Kafarski P; Berlicki Ł
J Med Chem; 2008 Sep; 51(18):5736-44. PubMed ID: 18717581
[TBL] [Abstract][Full Text] [Related]
16. Exploring new inhibitors of Plasmodium falciparum purine nucleoside phosphorylase.
Cui H; Ruda GF; Carrero-Lérida J; Ruiz-Pérez LM; Gilbert IH; González-Pacanowska D
Eur J Med Chem; 2010 Nov; 45(11):5140-9. PubMed ID: 20817362
[TBL] [Abstract][Full Text] [Related]
17. Piperidines: a new class of urease inhibitors.
Khan KM; Saify ZS; Arif Lodhi M; Butt N; Perveen S; Maharvi GM; Choudhary MI; Atta-Ur-Rahman
Nat Prod Res; 2006 May; 20(6):523-30. PubMed ID: 16835082
[TBL] [Abstract][Full Text] [Related]
18. Facile Solid-Phase Synthesis and Assessment of Nucleoside Analogs as Inhibitors of Bacterial UDP-Sugar Processing Enzymes.
Madec AGE; Schocker NS; Sanchini S; Myratgeldiyev G; Das D; Imperiali B
ACS Chem Biol; 2018 Sep; 13(9):2542-2550. PubMed ID: 30080379
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of fucosylated uridine conjugates as potential glycosyltransferase inhibitors.
Komor K; Szeja W; Komor R; Pastuch-Gawołek G; Thiem J
Acta Pol Pharm; 2014; 71(6):1083-9. PubMed ID: 25745784
[No Abstract] [Full Text] [Related]
20. Synthesis of uridine-5-propylamine derivatives and their use in affinity chromatography of N-acetylglucosaminyltransferases I and II.
Reck F
Carbohydr Res; 1995 Oct; 276(2):321-35. PubMed ID: 8542604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]