跳转到内容

丁酸睾酮

维基百科,自由的百科全书
丁酸睾酮
臨床資料
给药途径Intramuscular injection
识别信息
  • [(8R,9S,10R,13S,14S,17S)-10,13-Dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] butanoate
CAS号3410-54-6
PubChem CID
ChemSpider
UNII
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.020.270 編輯維基數據鏈接
化学信息
化学式C23H34O3
摩尔质量358.52 g·mol−1
3D模型(JSmol英语JSmol
  • CCCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C
  • InChI=1S/C23H34O3/c1-4-5-21(25)26-20-9-8-18-17-7-6-15-14-16(24)10-12-22(15,2)19(17)11-13-23(18,20)3/h14,17-20H,4-13H2,1-3H3/t17-,18-,19-,20-,22-,23-/m0/s1
  • Key:OMPTUWYLCDEFSJ-WAUHAFJUSA-N

丁酸睾酮(英語:Testosterone butyrate 或 testosterone butanoate)是睾酮的17β羟基丁酸,是一种人工合成的雄激素酯,最早在1930年代合成[1][2][3][4]

参考文献

[编辑]
  1. ^ Yalkowsky SH, He Y, Jain P. Handbook of Aqueous Solubility Data Second. CRC Press. 19 April 2016: 1288–. ISBN 978-1-4398-0246-5. 
  2. ^ Dorfman RI, Shipley RA. Androgens: biochemistry, physiology, and clinical significance. Wiley. 1956: 119. 
  3. ^ Koch FC. Recent advances in the field of androgens.. Cold Spring Harbor Symposia on Quantitative Biology (Cold Spring Harbor Laboratory Press). January 1937, 5: 34–43. doi:10.1101/SQB.1937.005.01.004. 
  4. ^ Griffiths PJ, James KC, Rees M. Crystallographic data for some testosterone esters. Acta Crystallographica. 1965, 19 (1): 149–150. ISSN 0365-110X. doi:10.1107/S0365110X65002918. 

外部链接

[编辑]