| 词条 | 6-Ketoprogesterone |
| 释义 |
| verifiedrevid = | ImageFile =6-Ketoprogesterone.svg | ImageSize = 200px | IUPACName = Pregn-4-ene-3,6,20-trione | OtherNames = 6-Ketoprogesterone;6-Oxoprogesterone |Section1={{Chembox Identifiers | CASNo=2243-08-5 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 2698PNJ55U | PubChem=104796 | SMILES = O=C4\\C=C3\\C(=O)C[C@@H]1[C@H](CC[C@@]2([C@@H](C(=O)C)CC[C@@H]12)C)[C@@]3(C)CC4 | InChI = 1/C21H28O3/c1-12(22)15-4-5-16-14-11-19(24)18-10-13(23)6-8-21(18,3)17(14)7-9-20(15,16)2/h10,14-17H,4-9,11H2,1-3H3/t14-,15+,16-,17-,20+,21+/m0/s1 | InChIKey = LASCNIPXMJNRGS-HGUQNLGYBS | StdInChI_Ref = | StdInChI = 1S/C21H28O3/c1-12(22)15-4-5-16-14-11-19(24)18-10-13(23)6-8-21(18,3)17(14)7-9-20(15,16)2/h10,14-17H,4-9,11H2,1-3H3/t14-,15+,16-,17-,20+,21+/m0/s1 | StdInChIKey_Ref = | StdInChIKey = LASCNIPXMJNRGS-HGUQNLGYSA-N | ChemSpiderID = 222301 | MeSHName = C111515 }} |Section2={{Chembox Properties | C=21 | H=28 | O=3 | Appearance= | Density=1.14 g/cm3 | MeltingPt= | BoilingPt= | Solubility= }} |Section3={{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = }} 6-Ketoprogesterone is an orally active oxidized form of progesterone that contains a keto group at position-6.[1]{{primary source inline|date=May 2014}} References1. ^{{cite journal | last1=Carlo|first1= J |last2= Pincus |first2= G. |last3= Carlo |first3= J. |last4= Romanoff |first4= E. B. |title= Isolation of an Unknown Substance and 6-Ketoprogesterone from Perfusates of Human Placentae|journal= Endocrinology|volume= 58 |issue= 3 |pages= 387 |date= March 1, 1956|doi=10.1210/endo-58-3-387 |pmid= 13294088 }} Further reading{{cite journal |author1=Paul B. Glickman, MD |author2=Robert H. Palmer, MD |author3=Attallah Kappas, MD |title= Steroid Fever And Inflammation |journal= Arch Intern Med |volume=114 |issue= 1|pages=46–58 |date=July 1964 | doi = 10.1001/archinte.1964.03860070092009}}{{DEFAULTSORT:Ketoprogesterone, 6-}}{{steroid-stub}} 1 : Pregnanes |
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