丁酸睾酮

丁酸睾酮
臨床資料
给药途径	Intramuscular injection
识别信息
	IUPAC命名法 [(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	102409;
ChemSpider	92494;
UNII	9RD3X2793Y;
CompTox Dashboard（英语：CompTox Chemicals Dashboard） (EPA)	DTXSID40955646 ;
ECHA InfoCard	100.020.270
化学信息
化学式	C23H34O3
摩尔质量	358.52 g·mol−1
3D模型（JSmol（英语：JSmol））	交互式图像;
	SMILES 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 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羟基的丁酸酯，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

^ Yalkowsky SH, He Y, Jain P. Handbook of Aqueous Solubility Data Second. CRC Press. 19 April 2016: 1288–. ISBN 978-1-4398-0246-5.
^ Dorfman RI, Shipley RA. Androgens: biochemistry, physiology, and clinical significance. Wiley. 1956: 119.
^ 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.
^ 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.