3α-Androstandiol

3α-Androstandiol
Nazivi
	IUPAC naziv (3R,5S,8R,9S,10S,13S,14S,17S)-10,13-dimetil-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradekahidro-1H-ciklopenta[a]fenantren-3,17-diol
	Drugi nazivi Hombreol
Identifikacija
CAS broj	1852-53-5;
3D model (Jmol)	interaktivna slika;
ChemSpider	15039;
ECHA InfoCard	100.015.862
PubChem C ID	15818;
	SMILES [H][C@]34[C@]2([H])CC[C@@]1([H])C[C@H](O)CC[C@@](C)1[C@]([H])2CC[C@@](C)3[C@@H](O)CC4; ; ; ; ; ;
Svojstva
Hemijska formula	C19H32O2
Molarna masa	292,46 g/mol
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	Reference infokutije

3α-Androstandiol (5α-androstan-3α,17β-diol) je androstandiol^[3] izveden iz DHT u reakciji koju katalizuje enzim 3-α-HSD.

Reference[uredi | uredi izvor]

^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. uredi
^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
^ Frye CA (2007). „Some rewarding effects of androgens may be mediated by actions of its 5alpha-reduced metabolite 3alpha-androstanediol”. Pharmacol. Biochem. Behav. 86 (2): 354—67. PMC 1857333 . PMID 17112575. doi:10.1016/j.pbb.2006.10.003.