177 related articles for article (PubMed ID: 25658064)
1. 'Click chemistry' synthesis of 1-(α-D-mannopyranosyl)-1,2,3-triazoles for inhibition of α-mannosidases.
Poláková M; Stanton R; Wilson IB; Holková I; Šesták S; Machová E; Jandová Z; Kóňa J
Carbohydr Res; 2015 Apr; 406():34-40. PubMed ID: 25658064
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of modified D-mannose core derivatives and their impact on GH38 α-mannosidases.
Poláková M; Horák R; Šesták S; Holková I
Carbohydr Res; 2016 Jun; 428():62-71. PubMed ID: 27152630
[TBL] [Abstract][Full Text] [Related]
3. 1,4-Dideoxy-1,4-imino-D- and L-lyxitol-based inhibitors bind to Golgi α-mannosidase II in different protonation forms.
Kóňa J; Šesták S; Wilson IBH; Poláková M
Org Biomol Chem; 2022 Nov; 20(45):8932-8943. PubMed ID: 36322142
[TBL] [Abstract][Full Text] [Related]
4. Structure and kinetic investigation of Streptococcus pyogenes family GH38 alpha-mannosidase.
Suits MD; Zhu Y; Taylor EJ; Walton J; Zechel DL; Gilbert HJ; Davies GJ
PLoS One; 2010 Feb; 5(2):e9006. PubMed ID: 20140249
[TBL] [Abstract][Full Text] [Related]
5. N-Benzyl Substitution of Polyhydroxypyrrolidines: The Way to Selective Inhibitors of Golgi α-Mannosidase II.
Šesták S; Bella M; Klunda T; Gurská S; Džubák P; Wöls F; Wilson IBH; Sladek V; Hajdúch M; Poláková M; Kóňa J
ChemMedChem; 2018 Feb; 13(4):373-383. PubMed ID: 29323461
[TBL] [Abstract][Full Text] [Related]
6. α-D-mannose derivatives as models designed for selective inhibition of Golgi α-mannosidase II.
Poláková M; Šesták S; Lattová E; Petruš L; Mucha J; Tvaroška I; Kóňa J
Eur J Med Chem; 2011 Mar; 46(3):944-52. PubMed ID: 21295890
[TBL] [Abstract][Full Text] [Related]
7. Human lysosomal alpha-mannosidases exhibit different inhibition and metal binding properties.
Venkatesan M; Kuntz DA; Rose DR
Protein Sci; 2009 Nov; 18(11):2242-51. PubMed ID: 19722277
[TBL] [Abstract][Full Text] [Related]
8. Synthesis of N-benzyl substituted 1,4-imino-l-lyxitols with a basic functional group as selective inhibitors of Golgi α-mannosidase IIb.
Klunda T; Šesták S; Kóňa J; Poláková M
Bioorg Chem; 2019 Mar; 83():424-431. PubMed ID: 30428432
[TBL] [Abstract][Full Text] [Related]
9. Conformationally locked thiosugars as potent alpha-mannosidase inhibitors: synthesis, biochemical and docking studies.
Sivapriya K; Hariharaputran S; Suhas VL; Chandra N; Chandrasekaran S
Bioorg Med Chem; 2007 Sep; 15(17):5659-65. PubMed ID: 17574420
[TBL] [Abstract][Full Text] [Related]
10. D-mannonolactam amidrazone. A new mannosidase inhibitor that also inhibits the endoplasmic reticulum or cytoplasmic alpha-mannosidase.
Pan YT; Kaushal GP; Papandreou G; Ganem B; Elbein AD
J Biol Chem; 1992 Apr; 267(12):8313-8. PubMed ID: 1569086
[TBL] [Abstract][Full Text] [Related]
11. Insect midgut α-mannosidases from family 38 and 47 with emphasis on those of Tenebrio molitor.
Moreira NR; Cardoso C; Ribeiro AF; Ferreira C; Terra WR
Insect Biochem Mol Biol; 2015 Dec; 67():94-104. PubMed ID: 26187253
[TBL] [Abstract][Full Text] [Related]
12. Golgi α-mannosidase: opposing structures of
Drogalin A; Monteiro LS; Alves MJ; Castro TG
J Biomol Struct Dyn; 2024 Mar; 42(5):2714-2725. PubMed ID: 37158092
[TBL] [Abstract][Full Text] [Related]
13. Comparison of kifunensine and 1-deoxymannojirimycin binding to class I and II alpha-mannosidases demonstrates different saccharide distortions in inverting and retaining catalytic mechanisms.
Shah N; Kuntz DA; Rose DR
Biochemistry; 2003 Dec; 42(47):13812-6. PubMed ID: 14636047
[TBL] [Abstract][Full Text] [Related]
14. Mechanistic Insight into the Binding of Multivalent Pyrrolidines to α-Mannosidases.
Mirabella S; D'Adamio G; Matassini C; Goti A; Delgado S; Gimeno A; Robina I; Moreno-Vargas AJ; Šesták S; Jiménez-Barbero J; Cardona F
Chemistry; 2017 Oct; 23(58):14585-14596. PubMed ID: 28902965
[TBL] [Abstract][Full Text] [Related]
15. Marked differences in the swainsonine inhibition of rat liver lysosomal alpha-D-mannosidase, rat liver Golgi mannosidase II, and jack bean alpha-D-mannosidase.
Tulsiani DR; Broquist HP; Touster O
Arch Biochem Biophys; 1985 Jan; 236(1):427-34. PubMed ID: 3917650
[TBL] [Abstract][Full Text] [Related]
16. Synthesis and Preclinical Evaluation of Indole Triazole Conjugates as Microtubule Targeting Agents that are Effective against MCF-7 Breast Cancer Cell Lines.
Yele V; Pindiprolu SKSS; Sana S; Ramamurty DSVNM; Madasi JRK; Vadlamani S
Anticancer Agents Med Chem; 2021; 21(8):1047-1055. PubMed ID: 32981511
[TBL] [Abstract][Full Text] [Related]
17. The structure of bovine lysosomal alpha-mannosidase suggests a novel mechanism for low-pH activation.
Heikinheimo P; Helland R; Leiros HK; Leiros I; Karlsen S; Evjen G; Ravelli R; Schoehn G; Ruigrok R; Tollersrud OK; McSweeney S; Hough E
J Mol Biol; 2003 Mar; 327(3):631-44. PubMed ID: 12634058
[TBL] [Abstract][Full Text] [Related]
18. Conformational Analysis of the Mannosidase Inhibitor Kifunensine: A Quantum Mechanical and Structural Approach.
Males A; Raich L; Williams SJ; Rovira C; Davies GJ
Chembiochem; 2017 Aug; 18(15):1496-1501. PubMed ID: 28493500
[TBL] [Abstract][Full Text] [Related]
19. Identification of the active site nucleophile in jack bean alpha-mannosidase using 5-fluoro-beta-L-gulosyl fluoride.
Howard S; He S; Withers SG
J Biol Chem; 1998 Jan; 273(4):2067-72. PubMed ID: 9442045
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of 5-amino-5-deoxy-D-mannopyranose and 1,5-dideoxy-1,5-imino-D-mannitol, and inhibition of alpha- and beta-D-mannosidases.
Legler G; Jülich E
Carbohydr Res; 1984 May; 128(1):61-72. PubMed ID: 6234061
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
