Hydrocortisone hemisuccinate
{{Short description|Chemical compound}}
{{Drugbox
| Verifiedfields =
| Watchedfields =
| verifiedrevid =
| IUPAC_name = 4-[2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethoxy]-4-oxobutanoic acid
| image = Hydrocortisone hemisuccinate.svg
| width =
| tradename =
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =
| class = Corticosteroid; Glucocorticoid
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =
| CAS_number_Ref =
| CAS_number = 2203-97-6
| CAS_supplemental =
110-15-6 (succinic acid)
| ATC_prefix =
| ATC_suffix =
| ATC_supplemental =
| PubChem = 16623
| IUPHAR_ligand =
| DrugBank_Ref =
| DrugBank = DB14545
| ChemSpiderID_Ref =
| ChemSpiderID = 15760
| UNII = IHV1VP592V
| KEGG = D01442
| ChEBI = 31677
| ChEMBL = 977
| synonyms = Hydrocortisone hydrogen succinate; Hydrocortisone succinate; Cortisol 21-hemisuccinate; 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione 21-hemisuccinate
| C=25 | H=34 | O=8
| SMILES = C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2[C@H](C[C@]4([C@H]3CC[C@@]4(C(=O)COC(=O)CCC(=O)O)O)C)O
| StdInChI_Ref =
| StdInChI = 1S/C25H34O8/c1-23-9-7-15(26)11-14(23)3-4-16-17-8-10-25(32,24(17,2)12-18(27)22(16)23)19(28)13-33-21(31)6-5-20(29)30/h11,16-18,22,27,32H,3-10,12-13H2,1-2H3,(H,29,30)/t16-,17-,18-,22+,23-,24-,25-/m0/s1
| StdInChIKey_Ref =
| StdInChIKey = VWQWXZAWFPZJDA-CGVGKPPMSA-N
}}
Hydrocortisone hemisuccinate ({{abbrlink|USAN|United States Adopted Name}}), also known as hydrocortisone hydrogen succinate ({{abbrlink|BANM|British Approved Name}}) or simply hydrocortisone succinate and sold under the brand name Solu-Cortel among many others, is a synthetic glucocorticoid corticosteroid and a corticosteroid ester which is used for antiinflammatory and antiallergic indications.{{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=PA317|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=317–}}{{cite book|title=Index Nominum 2000: International Drug Directory|url=https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA526|year=2000|publisher=Taylor & Francis|isbn=978-3-88763-075-1|pages=526–}}{{cite book| vauthors = Morton IK, Hall JM |title=Concise Dictionary of Pharmacological Agents: Properties and Synonyms|url=https://books.google.com/books?id=tsjrCAAAQBAJ&pg=PA145|date=6 December 2012|publisher=Springer Science & Business Media|isbn=978-94-011-4439-1|pages=145–}}
See also
References
{{Reflist}}
{{Glucocorticoids and antiglucocorticoids}}
{{Glucocorticoid receptor modulators}}
{{Mineralocorticoid receptor modulators}}
Category:Corticosteroid esters
{{Steroid-stub}}