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Volumn 7, Issue 9, 2006, Pages 1356-1359

Design and synthesis of highly potent and selective pharmacological chaperones for the treatment of Gaucher's disease

Author keywords

Chemical chaperones; Drug design; Enzymes; Gaucher's disease; Iminosugar; Inhibitors

Indexed keywords

1 DEOXYNOJIRIMYCIN; 1,5 DIDEOXY 1,5 IMINO DEXTRO XYLITOL; ALPHA 1 C ALKYL 1 DEOXYNOJIRIMYCIN; ALPHA 1 C ALKYL 1 DEOXYNOJIRIMYCIN DERIVATIVE; ALPHA 1 C NONYL 1 DEOXYNOJIRIMYCIN; ALPHA GALACTOSIDASE; AMINOXYLOSE DERIVATIVE; CHAPERONE; ENZYME INHIBITOR; GLUCOSYLCERAMIDASE; GLYCOSIDASE; GLYCOSIDASE INHIBITOR; GLYCOSPHINGOLIPID; IMIGLUCERASE; IMINE; IMINOXYLITOL DERIVATIVE; MIGLUSTAT; N BUTYL DEOXYNOJIRIMYCIN 1; N NONYL 1 DEOXYNOJIRIMYCIN; RECOMBINANT ENZYME; UNCLASSIFIED DRUG; XYLITOL; XYLOSE;

EID: 33748556543     PISSN: 14394227     EISSN: 14397633     Source Type: Journal    
DOI: 10.1002/cbic.200600217     Document Type: Article
Times cited : (165)

References (33)
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    • note
    • DIX does not display any significant inhibitory activity against the following enzymes: yeast and rice a-glucosidases, almond β-glucosidases, human lysosomal α-glucosidase and rat intestinal isomaltase, sucrase and maltase.
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    • note
    • The low yields observed for the one-pot procedure to give 10 may be explained by the relative instability of the intermediate aldehyde or of the related cyclic hemiaminal under aqueous acidic conditions (see refs. [12a] and [15]). In sharp contrast to our findings in the sorbofuranose series, attempts to optimize the process have not been successful to date.
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    • note
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.