Tham khảo Trestolone

  1. 1 2 3 4 5 6 7 8 9 J. Elks (14 tháng 11 năm 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. tr. 888–. ISBN 978-1-4757-2085-3.
  2. 1 2 3 4 https://adisinsight.springer.com/drugs/800016155
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 Nieschlag E, Kumar N, Sitruk-Ware R (2013). “7α-methyl-19-nortestosterone (MENTR): the population council's contribution to research on male contraception and treatment of hypogonadism”. Contraception. 87 (3): 288–95. doi:10.1016/j.contraception.2012.08.036. PMID 23063338.
  4. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Sundaram K, Kumar N, Bardin CW (tháng 4 năm 1993). “7 alpha-methyl-nortestosterone (MENT): the optimal androgen for male contraception”. Ann. Med. 25 (2): 199–205. doi:10.3109/07853899309164168. PMID 8489761.
  5. 1 2 3 4 5 6 7 Corona G, Rastrelli G, Vignozzi L, Maggi M (2012). “Emerging medication for the treatment of male hypogonadism”. Expert Opin Emerg Drugs. 17 (2): 239–59. doi:10.1517/14728214.2012.683411. PMID 22612692.
  6. 1 2 Lyster SC, Duncan GW (tháng 7 năm 1963). “Anabolic, androgenic and myotropic activities of derivatives of 7alpha-methyl-19-nortestosterone”. Acta Endocrinol. 43: 399–411. doi:10.1530/acta.0.0430399. PMID 13931986.
  7. 1 2 Ma JB, Li ZS (1990). “[Synthesis of 4-substituted 17 beta-hydroxy-7 alpha-methyl-4-estren-3-one and their 17-acetates as antifertility compounds]”. Yao Xue Xue Bao (bằng tiếng Trung Quốc). 25 (1): 18–23. PMID 2363352.Quản lý CS1: ngôn ngữ không rõ (liên kết)
  8. 1 2 3 Sundaram K, Kumar N, Bardin CW (1994). “7 alpha-Methyl-19-nortestosterone: an ideal androgen for replacement therapy”. Recent Prog. Horm. Res. 49: 373–6. PMID 8146434.
  9. 1 2 MENT – project information from the Population Council
  10. ↑ Anderson RA, Wallace AM, Sattar N, Kumar N, Sundaram K (tháng 6 năm 2003). “Evidence for tissue selectivity of the synthetic androgen 7 alpha-methyl-19-nortestosterone in hypogonadal men”. J. Clin. Endocrinol. Metab. 88 (6): 2784–93. doi:10.1210/jc.2002-021960. PMID 12788888.
  11. ↑ Attardi BJ, Hild SA, Koduri S, Pham T, Pessaint L, Engbring J, Till B, Gropp D, Semon A, Reel JR (tháng 10 năm 2010). “The potent synthetic androgens, dimethandrolone (7α,11β-dimethyl-19-nortestosterone) and 11β-methyl-19-nortestosterone, do not require 5α-reduction to exert their maximal androgenic effects”. The Journal of Steroid Biochemistry and Molecular Biology. 122 (4): 212–8. doi:10.1016/j.jsbmb.2010.06.009. PMC 2949447. PMID 20599615.
  12. 1 2 3 García-Becerra R, Ordaz-Rosado D, Noé G, Chávez B, Cooney AJ, Larrea F (2012). “Comparison of 7α-methyl-19-nortestosterone effectiveness alone or combined with progestins on androgen receptor mediated-transactivation”. Reproduction. 143 (2): 211–9. doi:10.1530/REP-11-0171. PMID 22065861.
  13. ↑ Attardi BJ, Pham TC, Radler LC, Burgenson J, Hild SA, Reel JR (tháng 6 năm 2008). “Dimethandrolone (7,11β-dimethyl-19-nortestosterone) and 11β-methyl-19-nortestosterone are not converted to aromatic A-ring products in the presence of recombinant human aromatase”. The Journal of Steroid Biochemistry and Molecular Biology. 110 (3–5): 214–22. doi:10.1016/j.jsbmb.2007.11.009. PMC 2575079. PMID 18555683.
  14. ↑ Ojasoo T, Delettré J, Mornon JP, Turpin-VanDycke C, Raynaud JP (1987). “Towards the mapping of the progesterone and androgen receptors”. J. Steroid Biochem. 27 (1–3): 255–69. doi:10.1016/0022-4731(87)90317-7. PMID 3695484.
  15. ↑ Delettré J, Mornon JP, Lepicard G, Ojasoo T, Raynaud JP (tháng 1 năm 1980). “Steroid flexibility and receptor specificity”. J. Steroid Biochem. 13 (1): 45–59. doi:10.1016/0022-4731(80)90112-0. PMID 7382482.
  16. ↑ Raynaud JP, Bouton MM, Moguilewsky M, Ojasoo T, Philibert D, Beck G, Labrie F, Mornon JP (tháng 1 năm 1980). “Steroid hormone receptors and pharmacology”. J. Steroid Biochem. 12: 143–57. doi:10.1016/0022-4731(80)90264-2. PMID 7421203.
  17. ↑ Ojasoo T, Raynaud JP, Doé JC (tháng 1 năm 1994). “Affiliations among steroid receptors as revealed by multivariate analysis of steroid binding data”. J. Steroid Biochem. Mol. Biol. 48 (1): 31–46. doi:10.1016/0960-0760(94)90248-8. PMID 8136304.
  18. ↑ Raynaud, J.P.; Ojasoo, T.; Bouton, M.M.; Philibert, D. (1979). “Receptor Binding as a Tool in the Development of New Bioactive Steroids”. Drug Design. tr. 169–214. doi:10.1016/B978-0-12-060308-4.50010-X. ISBN 9780120603084.
  19. 1 2 Attardi BJ, Hild SA, Reel JR (tháng 6 năm 2006). “Dimethandrolone undecanoate: a new potent orally active androgen with progestational activity”. Endocrinology. 147 (6): 3016–26. doi:10.1210/en.2005-1524. PMID 16497801. The pharmacokinetic properties of MENT make it unsuitable for once-daily oral treatment or long-term injection; thus, administration by sc implant or by patch or gel is required (27). MENT showed a more rapid metabolic clearance rate than T in men and monkeys, probably due in part to its failure to bind SHBG (28). In monkeys, MENT acetate in subdermal implants was 10 times as potent as T in suppression of gonadotropin secretion and anabolic effects, but was only twice as potent in stimulating prostate growth (29).
  20. ↑ Suvisaari J, Sundaram K, Noé G, Kumar N, Aguillaume C, Tsong YY, Lähteenmäki P, Bardin CW (tháng 5 năm 1997). “Pharmacokinetics and pharmacodynamics of 7alpha-methyl-19-nortestosterone after intramuscular administration in healthy men”. Hum. Reprod. 12 (5): 967–73. doi:10.1093/humrep/12.5.967. PMID 9194649.
  21. ↑ Kumar N, Didolkar AK, Ladd A, Thau R, Monder C, Bardin CW, Sundaram K (tháng 11 năm 1990). “Radioimmunoassay of 7 alpha-methyl-19-nortestosterone and investigation of its pharmacokinetics in animals”. J. Steroid Biochem. Mol. Biol. 37 (4): 587–91. doi:10.1016/0960-0760(90)90405-a. PMID 2278844.