Formebolona (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Formebolona" in Spanish language version.

refsWebsite

Global rank Spanish rank

7nih.gov

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6doi.org

2^nd place

3books.google.com

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7^th place

2semanticscholar.org

11^th place

79^th place

books.google.com

Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 471-. ISBN 978-3-88763-075-1.
J. Elks (14 de noviembre de 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 577-. ISBN 978-1-4757-2085-3.
I.K. Morton; Judith M. Hall (31 de octubre de 1999). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 125-. ISBN 978-0-7514-0499-9.

doi.org

dx.doi.org

Gelli D, Vignati E (1976). «Metabolic studies with formebolone (2-formyl-17 (alpha)-methyl-androsta-1,4-diene-11 (alpha), 17 (beta)-diol-3-one) in humans». J. Int. Med. Res. 4 (2): 96-105. PMID 799985. S2CID 86157607. doi:10.1177/030006057600400203.
Felippone F, Resnati G, Scolastico C, Tronconi G (1984). «Synthesis of 2-carboxy-11 beta, 17 beta-dihydroxy-17-methyl-1, 4-androstadien-3-one and related compounds». Steroids 43 (3): 271-82. PMID 6523544. S2CID 54289377. doi:10.1016/0039-128x(84)90045-x.
Dahlberg E, Snochowski M, Gustafsson JA (1981). «Regulation of the androgen and glucocorticoid receptors in rat and mouse skeletal muscle cytosol». Endocrinology 108 (4): 1431-40. PMID 6970661. doi:10.1210/endo-108-4-1431.
Souness GW, Latif SA, Laurenzo JL, Morris DJ (1995). «11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2), confer marked mineralocorticoid activity on corticosterone in the ADX rat». Endocrinology 136 (4): 1809-12. PMID 7895695. doi:10.1210/endo.136.4.7895695.
Souness GW, Morris DJ (1996). «11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase, possess hypertensinogenic activity in the rat». Hypertension 27 (3 Pt 1): 421-5. PMID 8698448. doi:10.1161/01.hyp.27.3.421.
Fürstenberger C, Vuorinen A, Da Cunha T, Kratschmar DV, Saugy M, Schuster D, Odermatt A (2012). «The anabolic androgenic steroid fluoxymesterone inhibits 11β-hydroxysteroid dehydrogenase 2-dependent glucocorticoid inactivation». Toxicol. Sci. 126 (2): 353-61. PMID 22273746. doi:10.1093/toxsci/kfs022.

nih.gov

ncbi.nlm.nih.gov

Gelli D, Vignati E (1976). «Metabolic studies with formebolone (2-formyl-17 (alpha)-methyl-androsta-1,4-diene-11 (alpha), 17 (beta)-diol-3-one) in humans». J. Int. Med. Res. 4 (2): 96-105. PMID 799985. S2CID 86157607. doi:10.1177/030006057600400203.
Cerutti S, Forlani A, Galimberti E (1976). «Anticatabolic action of formebolone in the castrated rat treated with dexamethasone». Arzneimittelforschung 26 (9): 1673-7. PMID 1036699.
Felippone F, Resnati G, Scolastico C, Tronconi G (1984). «Synthesis of 2-carboxy-11 beta, 17 beta-dihydroxy-17-methyl-1, 4-androstadien-3-one and related compounds». Steroids 43 (3): 271-82. PMID 6523544. S2CID 54289377. doi:10.1016/0039-128x(84)90045-x.
Dahlberg E, Snochowski M, Gustafsson JA (1981). «Regulation of the androgen and glucocorticoid receptors in rat and mouse skeletal muscle cytosol». Endocrinology 108 (4): 1431-40. PMID 6970661. doi:10.1210/endo-108-4-1431.
Souness GW, Latif SA, Laurenzo JL, Morris DJ (1995). «11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2), confer marked mineralocorticoid activity on corticosterone in the ADX rat». Endocrinology 136 (4): 1809-12. PMID 7895695. doi:10.1210/endo.136.4.7895695.
Souness GW, Morris DJ (1996). «11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase, possess hypertensinogenic activity in the rat». Hypertension 27 (3 Pt 1): 421-5. PMID 8698448. doi:10.1161/01.hyp.27.3.421.
Fürstenberger C, Vuorinen A, Da Cunha T, Kratschmar DV, Saugy M, Schuster D, Odermatt A (2012). «The anabolic androgenic steroid fluoxymesterone inhibits 11β-hydroxysteroid dehydrogenase 2-dependent glucocorticoid inactivation». Toxicol. Sci. 126 (2): 353-61. PMID 22273746. doi:10.1093/toxsci/kfs022.

semanticscholar.org

api.semanticscholar.org

Gelli D, Vignati E (1976). «Metabolic studies with formebolone (2-formyl-17 (alpha)-methyl-androsta-1,4-diene-11 (alpha), 17 (beta)-diol-3-one) in humans». J. Int. Med. Res. 4 (2): 96-105. PMID 799985. S2CID 86157607. doi:10.1177/030006057600400203.
Felippone F, Resnati G, Scolastico C, Tronconi G (1984). «Synthesis of 2-carboxy-11 beta, 17 beta-dihydroxy-17-methyl-1, 4-androstadien-3-one and related compounds». Steroids 43 (3): 271-82. PMID 6523544. S2CID 54289377. doi:10.1016/0039-128x(84)90045-x.