| 词条 | Tetrahydrocortisone |
| 释义 |
| Verifiedfields = changed | verifiedrevid = 470604200 | ImageFile=Tetrahydrocortisone.png | ImageSize=200px | IUPACName=(3R,5R,8S,9S,10S,13S,14S,17R)-3,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-11-one | OtherNames=Urocortisone; 3alpha,17,21-Trihydroxypregnane-11,20-dione |Section1={{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 5657 | InChI = 1/C21H32O5/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/h12-15,18,22-23,26H,3-11H2,1-2H3/t12-,13-,14+,15+,18-,19+,20+,21+/m1/s1 | InChIKey = SYGWGHVTLUBCEM-ZIZPXRJBBU | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C21H32O5/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/h12-15,18,22-23,26H,3-11H2,1-2H3/t12-,13-,14+,15+,18-,19+,20+,21+/m1/s1 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = SYGWGHVTLUBCEM-ZIZPXRJBSA-N | CASNo_Ref = {{cascite|changed|??}} | CASNo=53-05-4 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 1908043 | PubChem=5866 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 5HF9TM2D15 | SMILES = O=C2[C@H]3[C@H]([C@@H]1CC[C@](O)(C(=O)CO)[C@@]1(C)C2)CC[C@@H]4C[C@H](O)CC[C@]34C }} |Section2={{Chembox Properties | Formula=C21H32O5 | MolarMass=364.48 g/mol | Appearance= | Density= | MeltingPt= | BoilingPt= | Solubility= |Section3={{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = }}Tetrahydrocortisone, or urocortisone, is a steroid and an inactive metabolite of cortisone.[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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