CAS 1852-49-9
:5B-pregnane-3A-20A-diol glucuronide*cristallin
- Pregnanediol-3alpha-glucuronide
- 20alpha-Hydroxy-5beta-pregnan-3alpha-yl-beta-D-glucopyranosiduronic acid
- 5beta-Pregnane-3alpha,20alpha-diol-3alpha-glucuronide
- Pregnanediol-3-glucuronide
- (3alpha,5beta,20S)-20-Hydroxypregnan-3-yl beta-D-glucopyranosiduronic acid
- beta-D-Glucopyranosiduronic acid, (3alpha,5beta,20S)-20-hydroxypregnan-3-yl
Pregnanediol 3α-O-β-D-glucuronide
CAS :Pregnanediol 3α-O-β-D-glucuronide is a glucuronide metabolite of progesterone, which is a key steroid hormone in the reproductive system. This compound is derived from the metabolic conversion of progesterone, primarily within the liver, where it undergoes glucuronidation. This process involves the addition of glucuronic acid, mediated by the enzyme UDP-glucuronosyltransferase, enhancing the compound’s solubility for renal excretion.
Formule :C27H44O8Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :496.63 g/molPregnanediol 3a-O-b-D-Glucuronide
CAS :Produit contrôléApplications Pregnanediol 3α-O-β-D-Glucuronide is the glucuronide conjugate of Pregnanediol (P705130). Levels of Pregnanediol 3α-O-β-D-Glucuronide can be used to monitor the reproductive status of dairy cows. 3α-O-β-D-Glucuronide can be used (as an alternative to creatine) as a reference to adjust other hormonal markers in study of urinary hormonal profiles in the human menstrual cycle.
References Yang, C.J. et al.: Asian-Austral. J. Anim. Sci., 17, 460 (2004); Miro, F. et al.: Clin. Chem. Lab. Med., 42, 1043 (2004);Formule :C27H44O8Couleur et forme :NeatMasse moléculaire :496.63Pregnanediol-d5 3α-O-β-D-Glucuronide
CAS :Produit contrôléFormule :C27D5H39O8Couleur et forme :NeatMasse moléculaire :501.664Pregnanediol 3α-O-β-D-glucuronide
CAS :Pregnanediol 3α-O-β-D-glucuronide is a steroid conjugate, which is primarily a urinary metabolite derived from the catabolism of progesterone. It represents an important biomarker in endocrinological studies with direct relevance to reproductive biology. The compound originates in the body during the breakdown of progesterone, where it is conjugated with glucuronic acid to increase its solubility for renal excretion. This transformation allows for convenient and non-invasive monitoring of progesterone levels in clinical and research settings.
Formule :C27H44O8Degré de pureté :Min. 95 Area-%Masse moléculaire :496.64 g/mol




