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11β,17α,20β,21-tetrahydroxy-6α-methylpregna-1,4-diene-3-one is a steroid compound derived from the pregnane family, characterized by the presence of four hydroxyl groups at the 11β, 17α, 20β, and 21 positions, and a methyl group at the 6α position. It exhibits anti-inflammatory and antioxidant properties, as well as neuroprotective effects.
Used in Pharmaceutical Industry:
11β,17α,20β,21-tetrahydroxy-6α-methylpregna-1,4-diene-3-one is used as a glucocorticoid for its anti-inflammatory and antioxidant properties, helping to attenuate apoptosis in oligodendrocytes after injury and providing neuroprotection.
Used in Impurity Analysis:
11β,17α,20β,21-tetrahydroxy-6α-methylpregna-1,4-diene-3-one is used as an impurity in the analysis and production of 6α-Methyl Prednisolone (M325930), a glucocorticoid with similar therapeutic properties. Monitoring and controlling the levels of this impurity ensure the quality, safety, and efficacy of the final pharmaceutical product.

387-66-6

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387-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 387-66-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 387-66:
(5*3)+(4*8)+(3*7)+(2*6)+(1*6)=86
86 % 10 = 6
So 387-66-6 is a valid CAS Registry Number.

387-66-6Upstream product

387-66-6Downstream Products

387-66-6Relevant academic research and scientific papers

Using complementary mass spectrometric approaches for the determination of methylprednisolone metabolites in human urine

Pozo, Oscar J.,Marcos, Josep,Matabosch, Xavier,Ventura, Rosa,Segura, Jordi

experimental part, p. 541 - 553 (2012/06/01)

RATIONALE The metabolism of methylprednisolone is revisited in order to find new metabolites that could be important for distinguishing between different routes of administration. Recently developed liquid chromatography/tandem mass spectrometry (LC/MS/MS) strategies for the detection of corticosteroid metabolites have been applied to the study of methylprednisolone metabolism. METHODS The structures of these metabolites were studied using two complementary mass spectrometric techniques: LC/MS/MS in product ion scan mode with electrospray ionization and gas chromatography/mass spectrometry (GC/MS) in full scan mode with electron ionization. Metabolites were also isolated by semipreparative liquid chromatography fractionation. Each fraction was divided into two aliquots; one was studied by LC/MS/MS and the other by GC/MS after methoxyamine-trimethylsilyl derivatization. RESULTS The combination of all the structural information allowed us to propose a comprehensive picture of methylprednisolone metabolism in humans. Overall, 15 metabolites including five previously unreported compounds have been detected. Specifically, 16β,17α,21-trihydroxy-6α-methylpregna-1,4-diene- 3,11,20-trione, 17α,20β,21-trihydroxy-6α-methylpregna-1,4- diene-3, 11-dione, 11β,17α,21-trihydroxy-6α- hydroxymethylpregna-1,4-diene-3,20-dione, 11β,17α,20,21-tetrahydroxy- 6α-hydroxymethylpregna-1,4-diene-3-one, and 17α,21-dihydroxy- 6α-hydroxymethylpregna-1,4-diene-3,11,20-trione are proposed as feasible structures for the novel metabolites. In addition to the expected biotransformations: reduction of the C20 carbonyl, oxidation of the C11 hydroxy group, and further 6β-hydroxylation, we propose that hydroxylation of the 6α-methyl group can also take place. CONCLUSIONS New metabolites have been identified in urine samples collected after oral administration of 40mg of methylprednisolone. All identified metabolites were found in all samples collected up to 36h after oral administration. However, after topical administration of 5g of methylprednisolone aceponate, neither the parent compound nor any of the metabolites were detected. Copyright

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