General Information of This Metabolic Reaction (MR) (ID: MR012916)
Formula
SVG example
Reactant NSC-63853 Product Cortisol
Reactant Info Product Info
Other MR(s) Related to The Reactant of This MR
Other MR(s) That Metabolize The Reactant of This MR
MR ID Reactant Product MR Type Related Drug REF
MR012911 NSC-63853 17-alpha-hydroxyprogesterone Unclear NSC-63853 [1]
MR012915 NSC-63853 Androsterone Unclear NSC-63853 [2]
MR012912 NSC-63853 Dehydroepiandrosterone Unclear NSC-63853 [3]
MR012914 NSC-63853 Etiocholanolone Unclear NSC-63853 [2]
MR012913 NSC-63853 Isoandrosteron Unclear NSC-63853 [2]
Other MR(s) Related to The Product of This MR
Other MR(s) That Produce The Product of This MR
MR ID Reactant Product MR Type Related Drug REF
MR010825 Cortisone Cortisol Unclear - Unclear Cortisone [4]
MR005759 Cortisone acetate Cortisol Unclear Cortisone acetate [5]
Other MR(s) That Metabolize The Produtc of This MR
MR ID Reactant Product MR Type Related Drug REF
MR010827 Cortisol Allo\tetrahydrocortisol (allo\THF) Unclear - Unclear Cortisone [4]
MR010826 Cortisol Tetrahydrocortisol (THF) Unclear - Unclear Cortisone [4]
References
1 CONVERSION OF 17-ALPHA-HYDROXYPREGNENOLONE TO 17-ALPHA-HYDROXYPROGESTERONE BY THE CANINE TESTIS IN VIVO
2 The conversion in vivo of 17-alpha-hydroxypregnenolone to dehydroisoandrosterone and other 17-ketosteroids
3 The role of cytochrome b5 in the biosynthesis of androgens by human P450c17
4 Long-term magnesium supplementation improves glucocorticoid metabolism: A post-hoc analysis of an intervention trial
5 Urinary steroid excretion after total adrenalectomy. III. Isolation and identification of the metabolites of cortisone acetate

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