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Volumn 63, Issue 9, 1998, Pages 464-469

Partial synthetic derivatization of canrenone and characterization of its impact on the inhibitory effect on Na+/K+-ATPase activity in human heart muscle

Author keywords

3 amino derivatives; 3 oxo 17 pregna 4,6 diene 21,17 carbolactone; 3 sulfonamido derivatives; Canrenone; Glycosidation; Hydrogenation; Na+ K+ ATPase inhibition; Reduction

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CANRENONE; CARDENOLIDE;

EID: 0031823875     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(98)00049-X     Document Type: Article
Times cited : (1)

References (30)
  • 2
    • 0027769225 scopus 로고
    • +-transporting ATPase as a step in the rational design of new inotropic steroids
    • +-transporting ATPase as a step in the rational design of new inotropic steroids. Prog Med Chem 30:135-202.
    • (1993) Prog Med Chem , vol.30 , pp. 135-202
    • Repke, K.R.H.1    Weiland, J.2    Megges, R.3    Schön, R.4
  • 3
    • 33847434364 scopus 로고    scopus 로고
    • Repke KRH, Schön R, Weiland J, Megges R, Nitz M, inventors. Neuartige Herzglykoside. DE Patent (DE-Offenlegungsschrift) 43 21 937. 1995
    • Repke KRH, Schön R, Weiland J, Megges R, Nitz M, inventors. Neuartige Herzglykoside. DE Patent (DE-Offenlegungsschrift) 43 21 937. 1995.
  • 4
    • 33748244021 scopus 로고
    • Digitalis research in Berlin-Buch: Retrospective and perspective views
    • Repke KRH, Megges R, Weiland J, Schön R (1995). Digitalis research in Berlin-Buch: Retrospective and perspective views. Angew Chem Int Ed Engl 34:282-294.
    • (1995) Angew Chem Int Ed Engl , vol.34 , pp. 282-294
    • Repke, K.R.H.1    Megges, R.2    Weiland, J.3    Schön, R.4
  • 6
    • 0015505031 scopus 로고
    • Direkte positiv-inotrope Herzwirkung von Aldactone (Spironolacton, Canrenoat-Kalium)
    • Schröder R, Ramdohr B, Hüttemann U, Schüren KP (1972). Direkte positiv-inotrope Herzwirkung von Aldactone (Spironolacton, Canrenoat-Kalium). Dtsch Med Wochenschr 97: 1535-1538.
    • (1972) Dtsch Med Wochenschr , vol.97 , pp. 1535-1538
    • Schröder, R.1    Ramdohr, B.2    Hüttemann, U.3    Schüren, K.P.4
  • 8
    • 0030587794 scopus 로고    scopus 로고
    • Effectiveness of spironolactone added to an angiotensin-converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure (The Randomized Aldactone Evaluation Study [RALES])
    • The RALES Investigators (1996). Effectiveness of spironolactone added to an angiotensin-converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure (The Randomized Aldactone Evaluation Study [RALES]). Am J Cardiol 78:902-907.
    • (1996) Am J Cardiol , vol.78 , pp. 902-907
  • 15
    • 0024430756 scopus 로고
    • 6,7-Dihydroxy-6,7-dihydrocanrenone isomers: Improved synthesis and proton NMR study
    • Tal DM (1989). 6,7-Dihydroxy-6,7-dihydrocanrenone isomers: Improved synthesis and proton NMR study. Steroids 54:113-122.
    • (1989) Steroids , vol.54 , pp. 113-122
    • Tal, D.M.1
  • 17
    • 33947292856 scopus 로고
    • Oxidations with silver carbonate/Celite. V. Oxidations of phenols and related compounds
    • Balogh V, Fétizon M, Golfier M (1971). Oxidations with silver carbonate/Celite. V. Oxidations of phenols and related compounds. J Org Chem 36:1339-1341.
    • (1971) J Org Chem , vol.36 , pp. 1339-1341
    • Balogh, V.1    Fétizon, M.2    Golfier, M.3
  • 18
    • 0000608011 scopus 로고
    • The reaction of tribenzoyl-α-L-rhamnopyranosyl bromide with methanol. Various benzoylated derivatives of L-rhamnose
    • Ness RK, Fletcher HG Jr, Hudson CS (1951). The reaction of tribenzoyl-α-L-rhamnopyranosyl bromide with methanol. Various benzoylated derivatives of L-rhamnose. J Am Chem Soc 73:296-300.
    • (1951) J Am Chem Soc , vol.73 , pp. 296-300
    • Ness, R.K.1    Fletcher Jr., H.G.2    Hudson, C.S.3
  • 19
    • 84981454923 scopus 로고
    • Protonenresonanzspektroskopie und Steroidstruktur. II. Die Lage der C-18- Und C-19- Methylsignale in Abhängigkeit von den Substituenten am Steroidgerüst
    • Zürcher RF (1963). Protonenresonanzspektroskopie und Steroidstruktur. II. Die Lage der C-18- und C-19- Methylsignale in Abhängigkeit von den Substituenten am Steroidgerüst. Helv Chim Acta 46:2054-2088.
    • (1963) Helv Chim Acta , vol.46 , pp. 2054-2088
    • Zürcher, R.F.1
  • 20
    • 33646279994 scopus 로고
    • The application of the method of molecular rotation differences to steroids. X. "β-Dihydroergosterol."
    • Barton DHR, Cox JD, Holness NJ (1949). The application of the method of molecular rotation differences to steroids. X. "β-Dihydroergosterol." J Chem Soc :1771-1779.
    • (1949) J Chem Soc , pp. 1771-1779
    • Barton, D.H.R.1    Cox, J.D.2    Holness, N.J.3
  • 21
    • 0004208435 scopus 로고
    • Reinhold, New York, and Chapman & Hall, London
    • Fieser LF, Fieser M (1959). Steroids. Reinhold, New York, and Chapman & Hall, London.
    • (1959) Steroids
    • Fieser, L.F.1    Fieser, M.2
  • 23
    • 37049175864 scopus 로고
    • Steroids. XIII. the conversion of ergosterol into progesterone
    • Johnson F, Newbold GT, Spring FS (1954). Steroids. XIII. The conversion of ergosterol into progesterone. J Chem Soc :1302-1306.
    • (1954) J Chem Soc , pp. 1302-1306
    • Johnson, F.1    Newbold, G.T.2    Spring, F.S.3
  • 24
    • 37049145008 scopus 로고
    • The synthesis of progesterone and related compounds
    • Daglish AF, Green J, Poole VD (1954). The synthesis of progesterone and related compounds. J Chem Soc :2627-2633.
    • (1954) J Chem Soc , pp. 2627-2633
    • Daglish, A.F.1    Green, J.2    Poole, V.D.3
  • 26
    • 0019844789 scopus 로고
    • Cardenolide analogues. 11. Improved method for the use of Fétizon's reagent in the synthesis of cardiac glycosides
    • Brown L, Boutagy J, Thomas R (1981). Cardenolide analogues. 11. Improved method for the use of Fétizon's reagent in the synthesis of cardiac glycosides. Arzneim-Forsch/Drug Res 31:1059-1064.
    • (1981) Arzneim-Forsch/Drug Res , vol.31 , pp. 1059-1064
    • Brown, L.1    Boutagy, J.2    Thomas, R.3
  • 27
    • 33847442309 scopus 로고    scopus 로고
    • Siemann HJ, Langbein G, Richter M, Chemnitius K, Hübler D, Heinze A, inventors. Verfahren zur Herstellung von Steroidamiden. DD Patent 296 502. 1991
    • Siemann HJ, Langbein G, Richter M, Chemnitius K, Hübler D, Heinze A, inventors. Verfahren zur Herstellung von Steroidamiden. DD Patent 296 502. 1991.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.