11-Deoxycorticosterone

CAS : 64-85-7

Ref. 3D-FD21043

Informations sur le produit

• Nom: 11-Deoxycorticosterone
• Synonymes: 4-Pregnen-21-ol-3,20-dione21-HydroxyprogesteroneCortexone, 11-Dehydroxycorticosterone, 11-Desoxycorticosterone, 21-Hydroxy-3,20-dioxopregn-4-ene, 21-Hydroxy-Δ4-pregnane-3,20-dione, 21-Hydroxy-Δ4-pregnene-3,20-dione, 21-Hydroxy-Δ⁴-pregnane-3,20-dione, 21-Hydroxy-Δ⁴-pregnene-3,20-dione, 21-Hydroxypregn-4-Ene-3,20-Dione, 21-Hydroxyprogesterone, 4-Pregnen-21-ol-3,20-dione, Cortexone, Corticosterone, 11-deoxy-, DOC, DOC (steroid), Deoxycorticosterone, Deoxycorticosterone Crystalline, Deoxycortone, Desoxicortona, Desoxycorton, Desoxycortone, Kendall's desoxy compound B, Nsc 11319, Pregn-4-ene-3,20-dione, 21-hydroxy-, Reichstein's substance Q, Δ4-Pregnene-21-ol-3,20-dione, Δ⁴-Pregnene-21-ol-3,20-dione

Description

11-Deoxycorticosterone is a mineralocorticoid that binds to the P2Y receptor. It has been shown that 11-deoxycorticosterone has no effect on blood pressure in low doses, but when given at high doses it can cause hypertension. The drug also causes some cardiac effects, such as increased heart rate and contraction force. 11-Deoxycorticosterone is metabolized by deoxycorticosterone acetate into carbenoxolone sodium and then excreted in the urine.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 330.46 g/mol
• Formule: C₂₁H₃₀O₃
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3/t15-,16-,17-,18+,20-,21-/m0/s1
• Code InChI: InChIKey=ZESRJSPZRDMNHY-YFWFAHHUSA-N
• SMILES: C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO