Methylprednisolone
A corticosteroid used to treat a wide range of inflammatory and autoimmune conditions, including allergic reactions, asthma flares, rheumatoid arthritis, and multiple sclerosis relapses. It is available in oral, injectable, and topical forms.
Khối lượng phân tử
374,4710 g/mol
LogP
1,90
TPSA
94,80 Ų
Lipinski RO5
Đạt
Lĩnh vực điều trị
Phân loại thuốc
Cơ chế tác dụng
Intermediate-acting synthetic glucocorticoid.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Intermediate-acting synthetic glucocorticoid.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
C[C@H]1C[C@@H]2[C@H]([C@@H](O)C[C@@]3(C)[C@H]2CC[C@]3(O)C(=O)CO)[C@@]2(C)C=CC(=O)C=C12
InChI
InChI=1S/C22H30O5/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3/t12-,14-,15-,17-,19+,20-,21-,22-/m0/s1
Molecular Formula
C22H30O5
HBD / HBA
3 / 5
Liên kết có thể quay
2
Nguyên tử nặng
27
Diltiazem inhibits CYP3A4-mediated methylprednisolone metabolism, increasing methylprednisolone exposure and the risk of steroid side effects including immunosuppression, hyperglycaemia, and hypertension.
Fluconazole inhibits CYP3A4-mediated metabolism of methylprednisolone, increasing its plasma levels and prolonging corticosteroid effects, raising the risk of Cushingoid features.
Methylprednisolone inhibits CYP3A4-mediated cyclosporine metabolism, raising cyclosporine levels; conversely, cyclosporine may increase methylprednisolone exposure — a bidirectional pharmacokinetic interaction.
No side effects recorded
Side effect data is not yet available for this drug.
Câu hỏi thường gặp
A corticosteroid used to treat a wide range of inflammatory and autoimmune conditions, including allergic reactions, asthma flares, rheumatoid arthritis, and multiple sclerosis relapses. It is available in oral, injectable, and topical forms.
Intermediate-acting synthetic glucocorticoid.
Key pharmacokinetic parameters for Methylprednisolone: Half-life: 18-36 hours.
Yes, Methylprednisolone is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
Related Drugs
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL650. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6741. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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