메뉴 건너뛰기




Volumn 2, Issue 7, 2007, Pages 992-994

Aminocyclitols as pharmacological chaperones for glucocerebrosidase, a defective enzyme in Gaucher disease

Author keywords

Chaperones; Cyclitols; Gaucher; Glucocerebrosidase; Glycolipids

Indexed keywords

CHAPERONE; CYCLITOL; GLUCOSYLCERAMIDASE; UNCLASSIFIED DRUG;

EID: 34548540634     PISSN: 18607179     EISSN: 18607187     Source Type: Journal    
DOI: 10.1002/cmdc.200700061     Document Type: Article
Times cited : (28)

References (30)
  • 13
    • 33747405125 scopus 로고    scopus 로고
    • Isofagomine derivatives: a H. H. Chang, N. Asano, S. Ishii, Y. Ichikawa, J. Q. Fan, FEBS J. 2006, 273, 4082-4092;
    • Isofagomine derivatives: a) H. H. Chang, N. Asano, S. Ishii, Y. Ichikawa, J. Q. Fan, FEBS J. 2006, 273, 4082-4092;
  • 16
    • 28044449165 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 7450-7453;
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 7450-7453
  • 18
    • 24644490499 scopus 로고    scopus 로고
    • Deoxynojirimycin derivatives: d P. Alfonso, S. Pampin, J. Estrada, J. C. Rodriguez-Rey, P. Giraldo, J. Sancho, M. Pocovi, Blood Cells Mol. Dis. 2005, 35, 268-276;
    • Deoxynojirimycin derivatives: d) P. Alfonso, S. Pampin, J. Estrada, J. C. Rodriguez-Rey, P. Giraldo, J. Sancho, M. Pocovi, Blood Cells Mol. Dis. 2005, 35, 268-276;
  • 20
    • 33748556543 scopus 로고    scopus 로고
    • see ref. [20]. Iminoxilitol derivatives: g P. Compain, O. R. Martin, C. Boucheron, G. Godin, L. Yu, K. Ikeda, N. Asano, ChemBioChem 2006, 7, 1356-1359.
    • f) see ref. [20]. Iminoxilitol derivatives: g) P. Compain, O. R. Martin, C. Boucheron, G. Godin, L. Yu, K. Ikeda, N. Asano, ChemBioChem 2006, 7, 1356-1359.
  • 21
    • 3242762183 scopus 로고    scopus 로고
    • Aminocyclitol derivatives: h H. Lin, Y. Sugimoto, Y. Ohsaki, H. Ninomiya, A. Oka, M. Taniguchi, H. Ida, Y. Eto, S. Ogawa, Y. Matsuzaki, M. Sawa, T. Inoue, K. Higaki, E. Nanba, K. Ohno, Y. Suzuki, Biochim. Biophys. Acta Mol. Basis Dis. 2004, 1689, 219-228.
    • Aminocyclitol derivatives: h) H. Lin, Y. Sugimoto, Y. Ohsaki, H. Ninomiya, A. Oka, M. Taniguchi, H. Ida, Y. Eto, S. Ogawa, Y. Matsuzaki, M. Sawa, T. Inoue, K. Higaki, E. Nanba, K. Ohno, Y. Suzuki, Biochim. Biophys. Acta Mol. Basis Dis. 2004, 1689, 219-228.
  • 25
    • 0023289451 scopus 로고    scopus 로고
    • Estimation of lipophilicity has been carried out according to Crippen's and Viswanadhan's fragmentation methods A. K. Ghose, G. M. Gripen, J. Chem. Inf. Comput. Sci. 1987, 27, 21
    • Estimation of lipophilicity has been carried out according to Crippen's and Viswanadhan's fragmentation methods (A. K. Ghose, G. M. Gripen, J. Chem. Inf. Comput. Sci. 1987, 27, 21
  • 26
    • 0024716284 scopus 로고
    • 163, respectively) using the integrated module provided by the Chem-Draw Ultra 9.0 package Cambridgesoft
    • and V. N. Viswanadhan, A. K. Ghose, G. R. Revankar, R. K. Robins, J. Chem. Inf. Comput. Sci. 1989, 29, 163, respectively) using the integrated module provided by the Chem-Draw Ultra 9.0 package (Cambridgesoft, 2004).
    • (1989) J. Chem. Inf. Comput. Sci , vol.29
    • Viswanadhan, V.N.1    Ghose, A.K.2    Revankar, G.R.3    Robins, R.K.4
  • 27
    • 8844262688 scopus 로고    scopus 로고
    • A similar correlation between chain length and GlucCerase inhibition has also been observed in isofagomine derivatives (ref [13c, and iminoxilitol derivatives (ref [13g, Likewise, this general trend has been observed in deoxynojirimycin derivatives on various glycosidases G. Godin, P. Compain, O. R. Martin, K. Ikeda, L. Yu, N. Asano, Bioorg. Med. Chem. Lett. 2004, 14, 5991-5995
    • A similar correlation between chain length and GlucCerase inhibition has also been observed in isofagomine derivatives (ref [13c]) and iminoxilitol derivatives (ref [13g]). Likewise, this general trend has been observed in deoxynojirimycin derivatives on various glycosidases (G. Godin, P. Compain, O. R. Martin, K. Ikeda, L. Yu, N. Asano, Bioorg. Med. Chem. Lett. 2004, 14, 5991-5995).
  • 28
    • 54849433969 scopus 로고    scopus 로고
    • i=2 nM, ref. [13g]). This last compound has been reported to double the residual activity in fibroblasts from Gaucher patients (ref. [13g]) at a concentration sensibly lower than that required for NNDNJ for a similar effect (ref. [14]).
    • i=2 nM, ref. [13g]). This last compound has been reported to double the residual activity in fibroblasts from Gaucher patients (ref. [13g]) at a concentration sensibly lower than that required for NNDNJ for a similar effect (ref. [14]).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.