11-Deoxy-17-hydroxycorticosterone

CAS : 152-58-9

Ref. 3D-FD21045

Informations sur le produit

• Nom: 11-Deoxy-17-hydroxycorticosterone
• Synonymes: Reichstein's Substance SCortexolone17,21-Dihydroxy-4-pregnene-3,20-dione, (8R,10R,13S,17R)-17-Hydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one, (8Xi,9Xi,10Xi,13Xi,14Xi)-17,21-Dihydroxypregn-4-Ene-3,20-Dione, 11-Deoxy-17-hydrocorticosterone, 11-Deoxycortisol, 11-Deoxycortisone, 11-Deoxyhydrocortisone, 11-Desoxy-17-hydroxycorticosterone, 11-Desoxy-17α-hydroxycorticosterone, 11-Desoxycortisol, 11-Desoxycortisone, 11-Desoxyhydrocortisone, 11-Dioxycortisol, 17,21-Dihydroxy-4-pregnene-3,20-dione, 17,21-Dihydroxy-Pregn-4-Ene-3,20-Dione, 17,21-Dihydroxypregn-4-en-3,20-dione, 17,21-Dihydroxypregn-4-ene-3,20-dione, 17,21-Dihydroxyprogesterone, 17-Hydroxy-11-deoxycorticosterone, 17alpha,21-Dihydroxypregn-4-ene-3,20-dione, 17Α,21-Dihydroxypregn-4-Ene-3,20-Dione, 17α,21-Dihydroxy-4-pregnen-3,20-dion, 17α,21-Dihydroxy-4-pregnen-3,20-dione, 17α,21-Dihydroxyprogesterone, 17α-Hydroxycortexone, 4-Pregnen-17α,21-diol-3,20-dion, 4-Pregnen-17α,21-diol-3,20-dione, 4-Pregnene-11β,17,21-triol-3,20-dione, 4-Pregnene-17α, 21-diol-3,20-dione, Compound S, Corticosterone, 11-deoxy-17-hydroxy-, Cortifen, Cortisol, 11-deoxy-, Cortisol, 11-dioxy-, Cortodoxon, Cortodoxona, Cortodoxone, Nsc 18317, Pregn-4-ene-3,20-dione, 17,21-dihydroxy-, Reichstein S, Reichstein substance S, Reichstein's Substanz S, Reichstein's compound S, Reichstein's substance S, Sk&F 3050, Skf 3050, Substance S, cortodoxone (INN), Δ4-Pregnene-17α,21-diol-3,20-dione, Δ⁴-Pregnene-17α,21-diol-3,20-dione, Cortexolone

Description

11-Deoxycorticosterone (11DOC) is a naturally occurring corticosteroid that has been studied as a potential treatment for cancer. 11DOC is an antagonist of the mineralocorticoid receptor, which regulates sodium and potassium ions in the body. It also inhibits lymphocyte transformation and cell nuclei. The 11DOC-induced tumor regression was found to be due to decreased cortisol concentrations and increased corticosterone concentration in the experimental model. Increased corticosterone concentration led to cell lysis, while decreased cortisol concentration inhibited inflammatory lesion growth. Structural analysis revealed that 11DOC binds to the mineralocorticoid receptor with high affinity, but does not bind with high affinity to the glucocorticoid receptor. This suggests that 11DOC may be used for tumor treatment without negative side effects such as hair loss or increased appetite.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 346.46 g/mol
• Formule: C₂₁H₃₀O₄
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: Powder