메뉴 건너뛰기




Volumn 45, Issue 5, 2010, Pages 1880-1897

Evaluation of 2-thioxo-2,3,5,6,7,8-hexahydropyrimido[4,5-d]pyrimidin-4(1H)-one analogues as GAA activators

Author keywords

Acid alpha glucosidase; Activation of GAA; Lysosomal storage disorder; Pompe disease

Indexed keywords

1 (3,4 DIMETHOXYPHENETHYL) 2 THIOXO 2,3 DIHYDROPTERIDIN 4(1H) ONE; 1 (3,4 DIMETHOXYPHENETHYL) 5,7 DIMETHYL 2 THIOXO 2,3 DIHYDROPYRIDO [2,3 D]PYRIMIDIN 4(1H) ONE; 1 (3,4 DIMETHOXYPHENETHYL) 6 PROPYL 2 THIOXO 2,3,5,6,7,8 HEXAHYDROPYRIMIDO[4,5-D]PYRIMIDIN 4(1H) ONE; 1 (3,4 DIMETHOXYPHENETHYL) 6 PROPYL 5,6,7,8 TETRAHYDROPYRIMIDO [4,5 D]PYRIMIDINE 2,4(1H,3 ) DIONE; 1 (3,4 DIMETHOXYPHENETHYL)UREA; 2 THIOXO 2,3 DIHYDROPYRIMIDIN 4(1H) ONE DERIVATIVE; 2 THIOXO 2,3,5,6,7,8 HEXAHYDROPYRIMIDO[4,5 D]PYRIMIDIN 4(1H) ONE; 3 (3,4 DIMETHOXYPHENETHYL) 2 THIOXO 2,3 DIHYDRO 1H PURIN 6(9H) ONE; 5 CHLORO 8 (PHENYLETHYNYL)PYRIDO[4,3 D]PYRIMIDINE; 5 CHLORO 8 [(3,4 DIMETHOXYPHENYL)ETHYNYL]PYRIDO[4,3 D]PYRIMIDINE; 5 CHLORO 8 IODOPYRIDO[4,3 D]PYRIMIDINE; 5,6 DIAMINO 1 (3,4 DIMETHOXYPHENETHYL) 2 THIOXO 2,3 DIHYDROPYRIMIDIN 4(1H) ONE; 6 AMINO 1 (3,4 DIMETHOXYPHENETHYL) 5 NITROSO 2 THIOXO 2, 3 DIHYDROPYRIMIDIN 4(1H) ONE; 6 AMINO 1 (3,4 DIMETHOXYPHENETHYL)PYRIMIDINE 2,4(1H,3H) DIONE; 8 (3,4 DIMETHOXYPHENETHYL)PYRIDO[4,3 D]PYRIMIDIN 5(6H) ONE; 8 (PHENYLETHYL)PYRIDO[4,3 D]PYRIMIDIN 5(6H) ONE; 8 (PHENYLETHYNYL)PYRIDO[4,3 D]PYRIMIDIN 5(6H) ONE; 8 [(3,4 DIMETHOXYPHENYL)ETHYNYL]PYRIDO[4,3 D]PYRIMIDIN 5(6H) ONE; 8 IODOPYRIDO[4,3 D]PYRIMIDIN 5 (6H) ONE; ALPHA GLUCOSIDASE; ALPHA GLUCOSIDASE INHIBITOR; CHAPERONE; ENZYME ACTIVATOR; MUTANT PROTEIN; PYRIDO[4,3 D]PYRIMIDIN 5(6H) ONE; UNCLASSIFIED DRUG;

EID: 77949654790     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2010.01.027     Document Type: Article
Times cited : (24)

References (29)
  • 1
    • 0000995321 scopus 로고    scopus 로고
    • Glycogen storage disease type II: acid α- glucosidase (acid maltase) deficiency
    • Scriver C.R., Beaudet A.L., Sly W.S., and Valle D. (Eds), McGraw-Hill, New York
    • Hirschhorn R., and Reuser A.J.J. Glycogen storage disease type II: acid α- glucosidase (acid maltase) deficiency. In: Scriver C.R., Beaudet A.L., Sly W.S., and Valle D. (Eds). The Metabolic and Molecular Bases of Inherited Disease (2001), McGraw-Hill, New York 3389-3420
    • (2001) The Metabolic and Molecular Bases of Inherited Disease , pp. 3389-3420
    • Hirschhorn, R.1    Reuser, A.J.J.2
  • 3
    • 77949659105 scopus 로고    scopus 로고
    • http://www.myozyme.com/
  • 4
    • 77949656762 scopus 로고    scopus 로고
    • http://www.rxlist.com/myozyme-drug.htm
  • 6
    • 77949659180 scopus 로고    scopus 로고
    • http://www.hgmd.cf.ac.uk
  • 15
    • 77949655966 scopus 로고    scopus 로고
    • V.U. Ahmad, M.I. Choudhary, N. Khan, S.N. Khan. US 2008/0274987.
    • V.U. Ahmad, M.I. Choudhary, N. Khan, S.N. Khan. US 2008/0274987.
  • 23
    • 77949653601 scopus 로고    scopus 로고
    • D. Pivonka, A.K. Tiden, J. Viklund. WO 2007/120097.
    • D. Pivonka, A.K. Tiden, J. Viklund. WO 2007/120097.
  • 24
    • 77949656938 scopus 로고
    • 1
    • M.C. Venuti. 1, 1982, pp. 61-63.
    • (1982) , pp. 61-63
    • Venuti, M.C.1
  • 27
    • 77949659791 scopus 로고    scopus 로고
    • O. Plettenburg, A. Hofmeister, D. Kadereit, J. Brendel, M. Lohn. WO 2007/012422.
    • O. Plettenburg, A. Hofmeister, D. Kadereit, J. Brendel, M. Lohn. WO 2007/012422.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.