186 related articles for article (PubMed ID: 19663423)
1. Total synthesis and structural revision of TMG-chitotriomycin, a specific inhibitor of insect and fungal beta-N-acetylglucosaminidases.
Yang Y; Li Y; Yu B
J Am Chem Soc; 2009 Sep; 131(34):12076-7. PubMed ID: 19663423
[TBL] [Abstract][Full Text] [Related]
2. Synthesis, evaluation, and mechanism of N,N,N-trimethyl-D-glucosamine-(1→4)-chitooligosaccharides as selective inhibitors of glycosyl hydrolase family 20 β-N-acetyl-D-hexosaminidases.
Yang Y; Liu T; Yang Y; Wu Q; Yang Q; Yu B
Chembiochem; 2011 Feb; 12(3):457-67. PubMed ID: 21290547
[TBL] [Abstract][Full Text] [Related]
3. Kinetic and thermodynamic insights into the inhibitory mechanism of TMG-chitotriomycin on Vibrio campbellii GH20 exo-β-N-acetylglucosaminidase.
Morimoto Y; Takahashi S; Isoda Y; Nokami T; Fukamizo T; Suginta W; Ohnuma T
Carbohydr Res; 2021 Jan; 499():108201. PubMed ID: 33243428
[TBL] [Abstract][Full Text] [Related]
4. TMG-chitotriomycin, an enzyme inhibitor specific for insect and fungal beta-N-acetylglucosaminidases, produced by actinomycete Streptomyces anulatus NBRC 13369.
Usuki H; Nitoda T; Ichikawa M; Yamaji N; Iwashita T; Komura H; Kanzaki H
J Am Chem Soc; 2008 Mar; 130(12):4146-52. PubMed ID: 18307344
[TBL] [Abstract][Full Text] [Related]
5. A straightforward access to TMG-chitooligomycins and their evaluation as β-N-acetylhexosaminidase inhibitors.
Halila S; Samain E; Vorgias CE; Armand S
Carbohydr Res; 2013 Mar; 368():52-6. PubMed ID: 23333949
[TBL] [Abstract][Full Text] [Related]
6. MS/MS fragmentation-guided search of TMG-chitooligomycins and their structure-activity relationship in specific β-N-acetylglucosaminidase inhibition.
Usuki H; Yamamoto Y; Kumagai Y; Nitoda T; Kanzaki H; Hatanaka T
Org Biomol Chem; 2011 Apr; 9(8):2943-51. PubMed ID: 21373681
[TBL] [Abstract][Full Text] [Related]
7. TMG-chitotriomycin as a probe for the prediction of substrate specificity of β-N-acetylhexosaminidases.
Shiota H; Kanzaki H; Hatanaka T; Nitoda T
Carbohydr Res; 2013 Jun; 375():29-34. PubMed ID: 23685037
[TBL] [Abstract][Full Text] [Related]
8. Automated electrochemical assembly of the protected potential TMG-chitotriomycin precursor based on rational optimization of the carbohydrate building block.
Nokami T; Isoda Y; Sasaki N; Takaiso A; Hayase S; Itoh T; Hayashi R; Shimizu A; Yoshida J
Org Lett; 2015 Mar; 17(6):1525-8. PubMed ID: 25756520
[TBL] [Abstract][Full Text] [Related]
9. From chitin to bioactive chitooligosaccharides and conjugates: access to lipochitooligosaccharides and the TMG-chitotriomycin.
Despras G; Alix A; Urban D; Vauzeilles B; Beau JM
Angew Chem Int Ed Engl; 2014 Oct; 53(44):11912-6. PubMed ID: 25212734
[TBL] [Abstract][Full Text] [Related]
10. Pochonicine, a polyhydroxylated pyrrolizidine alkaloid from fungus Pochonia suchlasporia var. suchlasporia TAMA 87 as a potent beta-N-acetylglucosaminidase inhibitor.
Usuki H; Toyo-oka M; Kanzaki H; Okuda T; Nitoda T
Bioorg Med Chem; 2009 Oct; 17(20):7248-53. PubMed ID: 19775896
[TBL] [Abstract][Full Text] [Related]
11. Efficient synthesis of the glucosidase inhibitor blintol, the selenium analogue of the naturally occurring glycosidase inhibitor salacinol.
Liu H; Pinto BM
J Org Chem; 2005 Jan; 70(2):753-5. PubMed ID: 15651838
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of all-cis 2,5-imino-2,5-dideoxy-fucitol and its evaluation as a potent fucosidase and galactosidase inhibitor.
Ak A; Prudent S; LeNouën D; Defoin A; Tarnus C
Bioorg Med Chem Lett; 2010 Dec; 20(24):7410-3. PubMed ID: 21050758
[TBL] [Abstract][Full Text] [Related]
13. Synthesis and biological evaluation of deoxy salacinols, the role of polar substituents in the side chain on the alpha-glucosidase inhibitory activity.
Muraoka O; Yoshikai K; Takahashi H; Minematsu T; Lu G; Tanabe G; Wang T; Matsuda H; Yoshikawa M
Bioorg Med Chem; 2006 Jan; 14(2):500-9. PubMed ID: 16198577
[TBL] [Abstract][Full Text] [Related]
14. alpha-Glucopyranoimidazolines as intermediate analogue inhibitors of family 20 beta-N-acetylglucosaminidases.
Kato M; Uno T; Hiratake J; Sakata K
Bioorg Med Chem; 2005 Mar; 13(5):1563-71. PubMed ID: 15698773
[TBL] [Abstract][Full Text] [Related]
15. Computational Study for the Unbinding Routes of β-
Hu S; Zhao X; Zhang L
Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30917577
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol.
Bhat RG; Kumar NS; Pinto BM
Carbohydr Res; 2007 Sep; 342(12-13):1934-42. PubMed ID: 17572396
[TBL] [Abstract][Full Text] [Related]
17. Iminoalditol-amino acid hybrids: synthesis and evaluation as glycosidase inhibitors.
Steiner AJ; Stütz AE; Tarling CA; Withers SG; Wrodnigg TM
Carbohydr Res; 2007 Sep; 342(12-13):1850-8. PubMed ID: 17442281
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes.
Choubdar N; Bhat RG; Stubbs KA; Yuzwa S; Pinto BM
Carbohydr Res; 2008 Jul; 343(10-11):1766-77. PubMed ID: 18358456
[TBL] [Abstract][Full Text] [Related]
19. Synthesis of a salacinol analogue and its alpha-glucosidase inhibitory activity.
Shao Y; Osamu M; Kazuya Y; Yoshiharu M; Eriko Y; Toshie M; Genzoh T; Hisashi M; Masayuki Y; You QD
Yao Xue Xue Bao; 2006 Jul; 41(7):647-53. PubMed ID: 17007358
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of D-lyxitol and D-ribitol analogues of the naturally occurring glycosidase inhibitor salacinol.
Kumar NS; Pinto BM
Carbohydr Res; 2005 Dec; 340(17):2612-9. PubMed ID: 16198322
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]