Hydrocortisone aceponate

Hydrocortisone aceponate
Clinical data
Trade namesCortavance, others
AHFS/Drugs.comMonograph
Routes of
administration
Topical
Drug classCorticosteroid
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismLiver
Elimination half-life6-8 hours
Identifiers
  • (11β)-21-(acetyloxy)-11-hydroxy-3,20-dioxopregn-4-en-17-yl propionate
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
ECHA InfoCard100.184.885 Edit this at Wikidata
Chemical and physical data
FormulaC26H36O7
Molar mass460.567 g·mol−1
3D model (JSmol)
  • CCC(=O)O[C@@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)O)C)C(=O)COC(=O)C
  • InChI=1S/C26H36O7/c1-5-22(31)33-26(21(30)14-32-15(2)27)11-9-19-18-7-6-16-12-17(28)8-10-24(16,3)23(18)20(29)13-25(19,26)4/h12,18-20,23,29H,5-11,13-14H2,1-4H3/t18-,19-,20-,23+,24-,25-,26-/m0/s1 ☒N
  • Key:MFBMYAOAMQLLPK-FZNHGJLXSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Hydrocortisone aceponate is a veterinary corticosteroid that is used in form of creams for the treatment of various dermatoses (skin conditions).[4] It is an ester of hydrocortisone (cortisol) with acetic acid and propionic acid.

  1. ^ Cite error: The named reference Easotic EPAR was invoked but never defined (see the help page).
  2. ^ Cite error: The named reference Cortavance EPAR was invoked but never defined (see the help page).
  3. ^ "Cortaderm EPAR". European Medicines Agency (EMA). 17 June 2022. Retrieved 9 February 2024.
  4. ^ Mukhopadhyay AK, Baghel V (2010). "A study to evaluate the efficacy and safety of hydrocortisone aceponate 0.127% lipophilic cream in steroid responsive dermatoses in Indian patients". Indian Journal of Dermatology, Venereology and Leprology. 76 (5): 591. doi:10.4103/0378-6323.69093. PMID 20827017.

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