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Volumn 11, Issue 5, 2003, Pages 663-673

Dantrolene analogues revisited: General synthesis and specific functions capable of discriminating two kinds of Ca2+ release from sarcoplasmic reticulum of mouse skeletal muscle

Author keywords

[No Author keywords available]

Indexed keywords

1 [(5 PHENYLFURFURYLIDENE)AMINO]IMIDAZOLIDINE 2 4 DIONE; 1 [[5 (1 NAPHTHYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (2 METHOXYPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (2 NITROPHENYL) 2 THENYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (2 NITROPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDENE 2,4 DIONE; 1 [[5 (2,3,4,5,6 PENTAFLUOROPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (2,6 DINITROPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (3 METHOXYPHENYL)FUFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (3 NITROPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 CYANOPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 FLUOROPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 HYDROXYPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 METHOXYPHENYL)FUFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 METHYLPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2 4 DIONE; 1 [[5 (4 NITROPHENYL) 2 THENYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 PHENYLPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 TRIFLUOROMETHANESUFONYLPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; 1 [[5 (4 TRIFLUOROMETHYLPHENYL)FURFURYLIDENE]AMINO]IMIDAZOLIDINE 2,4 DIONE; CALCIUM ION; DANTROLENE; GIF 0166; GIF 0185; GIF 0248; IMIDAZOLIDINE DERIVATIVE; SAPONIN; UNCLASSIFIED DRUG;

EID: 0037355263     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00600-4     Document Type: Article
Times cited : (63)

References (50)
  • 1
    • 0003968950 scopus 로고
    • R.M. Simmons. New York: Cambridge University Press
    • Simmons R.M. Muscular Contraction. 1992;Cambridge University Press, New York.
    • (1992) Muscular Contraction
  • 27
    • 4243737730 scopus 로고
    • (a) Akashi, H.; Oda, R. J. Chem. Soc. Japan 1950, 53, 81; Chem. Abstr. 1953, 47, 2164e.
    • (1953) Chem. Abstr. , vol.47
  • 30
    • 84981850322 scopus 로고
    • The low reproducibility for preparation of 5-phenyl-2-furaldehyde was reported: We also failed to prepare methoxy- or methyl-substituted dantrolene congeners by this method
    • The low reproducibility for preparation of 5-phenyl-2-furaldehyde was reported: Davis C.S., Lougheed G.S. J. Heterocycl. Chem. 4:1967;153. We also failed to prepare methoxy- or methyl-substituted dantrolene congeners by this method.
    • (1967) J. Heterocycl. Chem. , vol.4 , pp. 153
    • Davis, C.S.1    Lougheed, G.S.2
  • 32
    • 0033603416 scopus 로고    scopus 로고
    • (a) Other methods for the synthesis of 5-aryl-2-furaldehyde: Stille reaction using 7a protected with ethylene acetal: Balachari, D.; Quinn. L.; O'Doherty, G.A. Tetrahedron Lett. 1999, 40, 4769.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 4769
    • Balachari, D.1    Quinn, L.2    O'Doherty, G.A.3
  • 40
    • 0034662175 scopus 로고    scopus 로고
    • 3SnCl, -20°C to room temperature, 17 h, 91%. See also: Han, Y.; Roy, A.; Giroux, A. Tetrahedron Lett. 2000, 41, 5447.
  • 44
    • 0000299606 scopus 로고    scopus 로고
    • For inversed cross-coupling by the Suzuki reaction, namely, the combination of aryl boronic acids and 5-bromo-2-furaldehyde, see: Our method is favorable in terms of the ready availability of aryl substrates
    • For inversed cross-coupling by the Suzuki reaction, namely, the combination of aryl boronic acids and 5-bromo-2-furaldehyde, see: Bussolari J.C., Rehborn D.C. Org. Lett. 1:1999;965. Our method is favorable in terms of the ready availability of aryl substrates.
    • (1999) Org. Lett. , vol.1 , pp. 965
    • Bussolari, J.C.1    Rehborn, D.C.2
  • 50
    • 0012870381 scopus 로고    scopus 로고
    • For the inhibitory effect of 4-iodo congener of dantrolene (GIF-0146) on twitch contraction (35.6%), see ref 13.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.