| 词条 | Oxprenoic acid |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = 3-[(7R,8R,9S,10R,13S,14S,17R)-17-Hydroxy-10,13-dimethyl-3-oxo-7-propyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoic acid | image = Oxprenoate.svg | width = | tradename = | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = | CAS_number = 786592-95-8 | CAS_supplemental = | class = Antimineralocorticoid | ATC_prefix = | ATC_suffix = | ATC_supplemental = | PubChem = 3034004 | IUPHAR_ligand = | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = 2298559 | UNII = 2JGY63UVRO | KEGG = | ChEBI = | ChEMBL = 2107003 | C=25 | H=38 | O=4 | SMILES = CCC[C@@H]1CC2=CC(=O)CC[C@@]2([C@@H]3[C@@H]1[C@@H]4CC[C@]([C@]4(CC3)C)(CCC(=O)O)O)C | StdInChI_Ref = | StdInChI = 1S/C25H38O4/c1-4-5-16-14-17-15-18(26)6-10-23(17,2)19-7-11-24(3)20(22(16)19)8-12-25(24,29)13-9-21(27)28/h15-16,19-20,22,29H,4-14H2,1-3H3,(H,27,28)/t16-,19+,20+,22-,23+,24+,25-/m1/s1 | StdInChIKey_Ref = | StdInChIKey = DNHCHRGCTVRAFT-JEHIOXJOSA-N | synonyms = Oxprenoate; 17α-Hydroxy-3-oxo-7α-propyl-17α-pregn-4-ene-21-carboxylic acid }}Oxprenoic acid, or oxprenoate, is a synthetic steroidal antimineralocorticoid which was never marketed.[1] See also
References1. ^{{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA922|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=922–}} {{Mineralocorticoid receptor modulators}}{{steroid-stub}} 5 : Alcohols|Antimineralocorticoids|Carboxylic acids|Ketones|Pregnanes |
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