A highly lipophilic form of aldosterone. isolation and characterization of an aldosterone dimer

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A highly lipophilic form of aldosterone obtained both from incubations of 18-hydroxycorticosterone with quartered rat adrenals and by treatment of aldosterone with acid, was identified as an aldosterone dimer based on its 1H, 13C NMR and mass spectra. © 1985.

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Detalles Bibliográficos
Autor principal: Cozza, E.N
Otros Autores: Lantos, C.P, Burton, G.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1985
Acceso en línea:Registro en Scopus
DOI
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
Biblioteca Central Dr. Luis F. Leloir (FCEN) de Universidad de Buenos Aires
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024 7 |2 cas  |a aldosterone, 52-39-1, 6251-69-0; Aldosterone, 52-39-1 
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100 1 |a Cozza, E.N. 
245 1 2 |a A highly lipophilic form of aldosterone. isolation and characterization of an aldosterone dimer 
260 |c 1985 
270 1 0 |m Burton, G.; Departamento de Química Orgáinica and UMYMFOR (CONICET-FCEN), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. 2, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Cozza, Burton, Ceballos, Lantos, Harnik, Scott, Eighteen-deoxyaldosterone and other less polar forms of 18-hydroxycorticosterone as aldosterone precursors in rat adrenals (1985) J. steroid Biochem., 22, pp. 665-672 
504 |a Bush, Methods of paper chromatography of steroids applicable to the study of steroids in mammalian blood and tissues (1952) Biochem. J., 50, pp. 370-378 
504 |a Bush, Willoughby, The excretion of allotetrahydrocortisol in human urine (1957) Biochem. J., 67, pp. 689-700 
504 |a Neher, (1964) Steroid Chromatography, p. 97. , Elsevier, Amsterdam 
504 |a Kliman, Peterson, Double isotope derivative assay of aldosterone in biological extracts (1960) J. biol. Chem., 235, pp. 1639-1648 
504 |a Aragonés, Gros, Lantos, Locascio, Less polar forms and derivatives of 18-hydroxycorticosterone (1978) J. steroid Biochem., 9, pp. 175-180 
504 |a Hampel, Peng, Pearlman, Pearlman, Acylation of [3H]corticosterone by acini from mammary gland of lactating rats (1978) J. biol. Chem., 253, pp. 8545-8553 
504 |a Mellon-Nussbaum, Ponticorvo, Lieberman, Characterization of the lipoidal derivatives of pregnenolone prepared by incubation of the steroid with adrenal mitochondria (1979) J. biol. Chem., 254, pp. 12500-12505 
504 |a Hochberg, Bandy, Ponticorvo, Lieberman, Detection in bovine adrenal cortex of a lipoidal substance that yields pregnenolone upon treatment with alkali (1977) Proc. natn. Acad. Sci. U.S.A., 74, pp. 941-945 
504 |a Mellon-Nussbaum, Hochberg, Biosynthesis of lipoidal derivatives of pregnenolone and dehydroisoandrosterone by the adrenal (1980) J. biol. Chem., 255, pp. 5566-5572 
504 |a Genard, Carbon-13 magnetic resonance spectra of aldosterone 18-hydroxycorticosterone and 18-hydroxyprogesterone (1978) Organic Magnetic Resonance, 11, pp. 478-480 
504 |a De Vries, De Jong, Chromatographie separation and mass spectrometric behaviour of two isomers of aldosterone (1980) J. steroid Biochem., 13, pp. 387-394 
504 |a Damasco, Lantos, The existence of two interconvertible forms of 18-hydroxycorticosterone: is one of them the active precursor of aldosterone? (1975) J. steroid Biochem., 6, pp. 69-74 
504 |a Harnik, Kashman, Morris, Synthesis of 3ga, 5α-tetrahydroaldosterone (1984) J. steroid Biochem., 20, pp. 1313-1320 
504 |a Lichtwald, Bauer, Soltek, Vecsei, Long known aldosterone derivative. A physiological product? (1984) Seventh International Congress oj Endocrinology, , Excerpta Medica, July 1–7 (1984), Quebec, Canada, Elsevier Science Publishers, Amsterdam, Communication No. 1412 
520 3 |a A highly lipophilic form of aldosterone obtained both from incubations of 18-hydroxycorticosterone with quartered rat adrenals and by treatment of aldosterone with acid, was identified as an aldosterone dimer based on its 1H, 13C NMR and mass spectra. © 1985.  |l eng 
593 |a Laboratorio de Esteroides, Departamento de Quimica Biológica, PRHOM (CONICET) Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria, Pab. 2, 1428 Buenos Aires, Argentina 
593 |a Departamento de Química Orgáinica and UMYMFOR (CONICET-FCEN), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. 2, 1428 Buenos Aires, Argentina 
690 1 0 |a ALDOSTERONE 
690 1 0 |a ADRENAL GLAND 
690 1 0 |a ANIMAL CELL 
690 1 0 |a DIMERIZATION 
690 1 0 |a ENDOCRINE SYSTEM 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RAT 
690 1 0 |a ALDOSTERONE 
690 1 0 |a ANIMAL 
690 1 0 |a CHROMATOGRAPHY, HIGH PRESSURE LIQUID 
690 1 0 |a MAGNETIC RESONANCE SPECTROSCOPY 
690 1 0 |a MALE 
690 1 0 |a RATS 
690 1 0 |a SPECTRUM ANALYSIS, MASS 
700 1 |a Lantos, C.P. 
700 1 |a Burton, G. 
773 0 |d 1985  |g v. 23  |h pp. 511-516  |k n. 4  |p J. Steroid Biochem.  |x 00224731  |t Journal of Steroid Biochemistry 
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856 4 0 |u https://doi.org/10.1016/0022-4731(85)90200-6  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00224731_v23_n4_p511_Cozza  |y Handle 
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999 |c 73077 

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