drocinonide
{{Short description|Chemical compound}}
{{Drugbox
| Verifiedfields =
| Watchedfields =
| verifiedrevid =
| IUPAC_name = (4aS,4bR,5S,6aS,6bS,9aR,10aS,10bS,12aS)-4b-Fluoro-6b-glycoloyl-5-hydroxy-4a,6a,8,8-tetramethylhexadecahydro-2H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one
| image = Drocinonide.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 = 2355-59-1
| CAS_supplemental =
| class = Corticosteroid; Glucocorticoid
| ATC_prefix =
| ATC_suffix =
| ATC_supplemental =
| PubChem = 20055479
| IUPHAR_ligand =
| DrugBank_Ref =
| DrugBank =
| ChemSpiderID_Ref =
| ChemSpiderID = 16736952
| UNII = 6UJ1P9T59P
| KEGG = D03910
| ChEBI =
| ChEMBL = 2104454
| C=24 | H=35 | F=1 | O=6
| SMILES = C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@]2([C@H](C[C@]4([C@H]3C[C@@H]5[C@]4(OC(O5)(C)C)C(=O)CO)C)O)F
| StdInChI_Ref =
| StdInChI = 1S/C24H35FO6/c1-20(2)30-19-10-16-15-6-5-13-9-14(27)7-8-21(13,3)23(15,25)17(28)11-22(16,4)24(19,31-20)18(29)12-26/h13,15-17,19,26,28H,5-12H2,1-4H3/t13-,15-,16-,17-,19+,21-,22-,23-,24+/m0/s1
| StdInChIKey_Ref =
| StdInChIKey = GZBONOYGBJSTHF-QLRNAMTQSA-N
| synonyms = 9α-Fluoro-11β,16α,17α,21-tetrahydroxy-5α-pregnane-3,20-dione cyclic 16,17-acetal with acetone; 9α-Fluoro-11β,21-dihydroxy-16α,17α-((1-methylethylidene)bis(oxy))-5α-pregnane-3,20-dione
}}
Drocinonide is a synthetic glucocorticoid corticosteroid which was never marketed.{{cite book | vauthors = Elks J |title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA471|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=471–}}
References
{{Reflist|2}}
{{Glucocorticoid receptor modulators}}
Category:Corticosteroid cyclic ketals
{{steroid-stub}}