11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate)

11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate) Basic information
Description
Product Name:11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate)
Synonyms:11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate);Hydrocortisone phosphate;21-Hydrocortisonephosphoric acid;Corphos;Corticosterone, 17-hydroxy-, 21-phosphate (6CI);Cortisol 21-monophosphate;Cortisol 21-phosphate;Cortisol phosphate
CAS:3863-59-0
MF:C21H31O8P
MW:442.44
EINECS:223-382-2
Product Categories:
Mol File:3863-59-0.mol
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate) Structure
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate) Chemical Properties
Boiling point 669.9±65.0 °C(Predicted)
density 1.42±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka1.67±0.10(Predicted)
Safety Information
MSDS Information
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate) Usage And Synthesis
DescriptionHydrocortisone phosphate (Hydrocortisone 21-phosphate), a glucocorticoid, is an orally active steroidal anti-inflammatory agent (SAID). Hydrocortisone phosphate inhibits the biological activities of IL-6 and IL-3 with IC50 values of 6.7 and 21.4 μM, respectively. Hydrocortisone phosphate can be used in the study of ulcerative colitis (UC).
OriginatorCorphos,Tilden Yates,US,1959
UsesGlucocorticoid.
DefinitionChEBI: A steroid phosphate that is the 21-O-phospho derivative of cortisol.
Manufacturing Process21-iodo-11β:17α-dihydroxypregn-4-ene-3,20-dione (5.0 g) in pure acetonitrile (125 ml) was mixed with a solution of 90% phosphoric acid (2.5 ml) and triethylamine (7.5 ml) in acetonitrile (125 ml) and boiled under reflux for 4 hours. The solvent was removed in vacuo and the residue, dissolved in ethanol (20 ml) and water (80 ml), was passed down a column of Zeo-Karb 225 (H+form) (60 g) made up in 20% alcohol. Elution was continued with 20% alcohol (50 ml), 50% alcohol (50 ml) and alcohol (150 ml). The eluate was at first cloudy, but by the end of the elution it was clear and nonacid.
The eluate was titrated to pH 7 with 0.972N NaOH (63 ml). Removal of solvent left a gum, which was boiled with methanol (400 ml) for 20 minutes. The solid insoluble inorganic phosphate was filtered off and washed with methanol (200 ml). The slightly cloudy filtrate was filtered again, and evaporated to dryness in vacuo. The residual gum dissolved readily in water (40 ml) and on addition of acetone (600 ml) to the solution a mixture of sodium salts of hydrocortisone 21-phosphate separated as a white solid. This was collected after 2 days, washed with acetone and dried at 100°C/0.l mm/2 hr to constant weight. Yield 4.45 g.
Brand nameHydrocortone (Merck).
Therapeutic FunctionGlucocorticoid
11beta,17,21-trihydroxypregn-4-ene-3,20-dione 21-(dihydrogen phosphate) Preparation Products And Raw materials
Raw materialsSodium hydroxide-->11a,16b,17,21-Tetrahydroxy-pregna-1,4-diene-3,20-dione-->Phosphoric acid
Hydrocortisone

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