11β-羟基睾酮

11β-羟基睾酮
	IUPAC名; 11β,17β-dihydroxyandrost-4-ene-3-one
识别
CAS号	1816-85-9
PubChem	114920
ChemSpider	102866
SMILES	C1C2=CC(CC[C@@]2([C@]3([C@H](C[C@]4([C@]([C@@]3(C1)[H])(CC[C@@H]4O)[H])C)O)[H])C)=O;
InChI	InChI=1S/C19H28O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h9,13-17,21-22H,3-8,10H2,1-2H3/t13-,14-,15-,16-,17+,18-,19-/m0/s1;
ChEBI	81481
KEGG	C18075
性质
化学式	C19H28O3
摩尔质量	304.42 g·mol−1
危险性
	GHS危险性符号;
GHS提示词	Danger
H-术语	H351, H360
P-术语	P201, P202, P281, P308+313, P405, P501
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

11β-羟基睾酮是一种内源性类固醇，是睾酮的代谢产物之一，由类固醇11β羟化酶（CYP11B1）转化睾酮而来[1][2][3]。

参见

Storbeck KH, Mostaghel EA. . Advances in Experimental Medicine and Biology. 2019, 1210: 239–277. ISBN 978-3-030-32655-5. PMID 31900912. doi:10.1007/978-3-030-32656-2_11. CYP11B1 and 2 have also been shown to 11β-hydroxylate T, yielding 11β-hydroxytestosterone (11OHT), though the levels produced by the adrenal are low due to the limited availability of adrenal derived T
Stárka L, Dušková M, Vítků J. . Physiological Research. September 2020, 69 (Suppl 2): S187–S192. PMID 33094617. doi:10.33549/physiolres.934516 .
Van Rooyen, D.; Gent, R.; Barnard, L.; Swart, A. C. . The Journal of Steroid Biochemistry and Molecular Biology. 2018, 178: 203–212. PMID 29277707. S2CID 3700135. doi:10.1016/j.jsbmb.2017.12.014.

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