| 词条 | Tetrahydrocortisol |
| 释义 |
| Verifiedfields = changed | verifiedrevid = 470604176 | ImageFile=tetrahydrocortisol.png | ImageSize=200px | IUPACName=2-hydroxy-1-[(3R,5R,8S,9S,10S,11S,13S,14S,17R)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethanone | OtherNames=Urocortisol |Section1={{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 5655 | InChI = 1/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18-,19+,20+,21+/m1/s1 | InChIKey = AODPIQQILQLWGS-GXBDJPPSBG | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18-,19+,20+,21+/m1/s1 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = AODPIQQILQLWGS-GXBDJPPSSA-N | CASNo_Ref = {{cascite|changed|??}} | CASNo=53-02-1 | PubChem=5864 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 28320 | SMILES = O=C(CO)[C@@]4(O)CC[C@H]3[C@H]2[C@@H]([C@@]1([C@@H](C[C@H](O)CC1)CC2)C)[C@@H](O)C[C@@]34C }} |Section2={{Chembox Properties | Formula=C21H34O5 | MolarMass=366.49 g/mol | Appearance= | Density= | MeltingPt= | BoilingPt= | Solubility= |Section3={{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = }}Tetrahydrocortisol, or urocortisol, is a steroid and an inactive metabolite of cortisol.[1] See also
References1. ^{{cite book|author1=Thomas L. Lemke|author2=David A. Williams|title=Foye's Principles of Medicinal Chemistry|url=https://books.google.com/books?id=Sd6ot9ul-bUC&pg=PA915|date=24 January 2012|publisher=Lippincott Williams & Wilkins|isbn=978-1-60913-345-0|pages=915–}} {{Endogenous steroids}}{{Steroid-stub}} 2 : Human metabolites|Corticosteroids |
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