| 词条 | Domoprednate |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = [(1R,4aS,4bS,10aR,10bS,11S,12aS)-1-Acetyl-11-hydroxy-10a,12a-dimethyl-8-oxo-2,3,4,4a,4b,5,6,10b,11,12-decahydrochrysen-1-yl] butanoate | image = Domoprednate.svg | width = 200px | tradename = Stermonid | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = Topical | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = | CAS_number = 66877-67-6 | CAS_supplemental = | class = Corticosteroid; Glucocorticoid | ATC_prefix = | ATC_suffix = | ATC_supplemental = | PubChem = 68868 | IUPHAR_ligand = | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = 62100 | UNII = 910G0QIM2M | KEGG = | ChEBI = | ChEMBL = 2106538 | C=26 | H=36 | O=5 | SMILES = CCCC(=O)O[C@@]1(CCC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)C=C[C@]34C)O)C)C(=O)C | StdInChI_Ref = | StdInChI = 1S/C26H36O5/c1-5-7-22(30)31-26(16(2)27)12-6-8-20-19-10-9-17-14-18(28)11-13-24(17,3)23(19)21(29)15-25(20,26)4/h11,13-14,19-21,23,29H,5-10,12,15H2,1-4H3/t19-,20-,21-,23+,24-,25-,26-/m0/s1 | StdInChIKey_Ref = | StdInChIKey = IYBYNRHXGXDDDS-VRRJBYJJSA-N | synonyms = Ro 12-7024; 11β-Hydroxy-D-homopregna-1,4-diene-3,20-dione 17α-butyrate }}Domoprednate (brand name Stermonid; developmental code name Ro 12-7024) is a synthetic glucocorticoid corticosteroid which was developed in the late 1970s and 1980s.[1][2][3][4][5] 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=PA465|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=465–}} {{Glucocorticoids and antiglucocorticoids}}{{Glucocorticoid receptor modulators}}{{steroid-stub}}2. ^{{cite journal | vauthors = Schmidt H, Hjorth N, Holm P | title = A randomized trial on the D-homosteroid domoprednate (Ro 12-7024) in the treatment of dermatoses | journal = Dermatologica | volume = 168 | issue = 3 | pages = 127–30 | year = 1984 | pmid = 6370748 | doi = | url = }} 3. ^{{cite journal | vauthors = Serup J, Holm P | title = Domoprednate (Stermonid), a topical D-homocorticosteroid, skin atrophy and telangiectasia. A double-blind, randomized comparison with hydrocortisone butyrate, betamethasone valerate, clobetasole propionate and placebo | journal = Dermatologica | volume = 170 | issue = 4 | pages = 189–94 | year = 1985 | pmid = 3888708 | doi = | url = }} 4. ^{{cite journal | vauthors = Christiansen JV, Foged E, Holm P, Jørgensen AS, Reymann F | title = The treatment of psoriasis with 0.1% domoprednate (a D-homocorticosteroid) and 0.1% betamethasone valerate ointment. A double-blind, randomized trial | journal = Dermatologica | volume = 170 | issue = 4 | pages = 195–8 | year = 1985 | pmid = 3888709 | doi = | url = }} 5. ^{{cite journal | vauthors = Schmidt H, Hjorth N, Holm P | title = Domoprednate, a new nonhalogenated topical steroid: comparison to hydrocortisone butyrate | journal = Dermatologica | volume = 175 | issue = 3 | pages = 145–7 | year = 1987 | pmid = 3653463 | doi = | url = }} 6 : Alcohols|Butyrate esters|Diketones|Esters|Glucocorticoids|Pregnanes |
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