| 词条 | Halocortolone |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (6S,8S,9R,10S,11S,13S,14S,16R,17S)-9-Chloro-6,11-difluoro-17-(2-hydroxyacetyl)-10,13,16-trimethyl-7,8,11,12,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthren-3-one | image = Halocortolone.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 = 24320-27-2 | CAS_supplemental = | class = Corticosteroid; Glucocorticoid | ATC_prefix = | ATC_suffix = | ATC_supplemental = | PubChem = 20056980 | IUPHAR_ligand = | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = 16736630 | UNII = Z9TL048W82 | KEGG = | ChEBI = | ChEMBL = 2106353 | C=22 | H=27 | Cl=1 | F=2 | O=3 | SMILES = C[C@@H]1C[C@H]2[C@@H]3C[C@@H](C4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@H]1C(=O)CO)C)F)Cl)C)F | StdInChI_Ref = | StdInChI = 1S/C22H27ClF2O3/c1-11-6-13-14-8-16(24)15-7-12(27)4-5-21(15,3)22(14,23)18(25)9-20(13,2)19(11)17(28)10-26/h4-5,7,11,13-14,16,18-19,26H,6,8-10H2,1-3H3/t11-,13+,14+,16+,18+,19-,20+,21+,22+/m1/s1 | StdInChIKey_Ref = | StdInChIKey = MBRXSOUHUFBPQC-RFPWEZLHSA-N | synonyms = 9α-Chloro-6α,11β-difluoro-21-hydroxy-16α-methylpregna-1,4-diene-3,20-dione }}Halocortolone is a synthetic glucocorticoid corticosteroid which was never marketed.[1] 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=PA618|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=618–}} {{Glucocorticoid receptor modulators}}{{steroid-stub}} 6 : Alcohols|Chloroarenes|Diketones|Fluoroarenes|Glucocorticoids|Pregnanes |
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