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Volumn 15, Issue 30, 2009, Pages 7310-7328

Dihydroxyacetone phosphate aldolase catalyzed synthesis of structurally diverse polyhydroxylated pyrrolidine derivatives and evaluation of their glycosidase inhibitory properties

Author keywords

Aldol reaction; Amino aldehydes; Cyclitols; Enzyme catalysis; Glycosidase inhibitors

Indexed keywords

ALDOL REACTION; AMINO ALDEHYDES; CYCLITOLS; ENZYME CATALYSIS; GLYCOSIDASE INHIBITORS;

EID: 67651067950     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200900838     Document Type: Article
Times cited : (56)

References (80)
  • 4
    • 33748191656 scopus 로고    scopus 로고
    • A. Varki, Cell 2006, 126, 841-845.
    • (2006) Cell , vol.126 , pp. 841-845
    • Varki, A.1
  • 13
    • 0033559148 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 750-770.
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 750-770
  • 29
    • 0142119368 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 4661 - 4664.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 4661-4664
  • 45
    • 67651026260 scopus 로고    scopus 로고
    • A full study on the inhibition activity against α-L-fucosidase from bovine kidney of 5 and 6 and its diasteromerically related pyrrolidine isomers will be published elsewhere.
    • A full study on the inhibition activity against α-L-fucosidase from bovine kidney of 5 and 6 and its diasteromerically related pyrrolidine isomers will be published elsewhere.
  • 46
    • 67651013877 scopus 로고    scopus 로고
    • In our hands, the inhibitory activity of 5 was higher than the value previously reported by Wang el al.[48
    • [48]
  • 51
    • 67651045007 scopus 로고    scopus 로고
    • In a control experiment the known α-L-fucosidase inhibitor, 1-deoxy-1-fuconojirimycin, was assayed giving a value of Ki= 4.9 nM in good agreement with that reported in the literature.[45
    • [45]
  • 69
    • 67651045006 scopus 로고    scopus 로고
    • Although the bound conformation of mannostatin A in structure 2F70 shows the thiomethyl group oriented away from the hydrophobic pocket constituted by residues F206, W415, and Y727 and towards the hydrophilic environment, a recent paper[62] from the group that originally deposited the structure points out that this was actually due to an experimental artifact and that a later structural determination under different conditions showed that the actual orientation of the thiomethyl group is towards the above mentioned hydrophobic pocket
    • [62] from the group that originally deposited the structure points out that this was actually due to an experimental artifact and that a later structural determination under different conditions showed that the actual orientation of the thiomethyl group is towards the above mentioned hydrophobic pocket.
  • 80
    • 65249157397 scopus 로고    scopus 로고
    • P. Labute, Proteins 2009, 75, 187-205.
    • (2009) Proteins , vol.75 , pp. 187-205
    • Labute, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.