Drug/Small Molecule:
methylprednisolone

2D structure

Overview

Generic Names: 6alpha-Methylprednisolone; Methyleneprednisolone; Methylprednisolon; Methylprednisolonum [INN-Latin]; Metilprednisolona [INN-Spanish]; Metilprednisolone [Dcit]
Trade Names: Artisone-Wyeth; Besonia; Dopomedrol; Esametone; Firmacort; Lemod; Medesone; Medixon; Medlone 21; Medrate; Medrol Adt Pak; Medrol Dosepak; Medrone; Mesopren; Metastab; Metilbetasone; Metrisone; Metrocort; Metysolon; Moderin; Nirypan; Noretona; Predni N Tablinen; Promacortine; Reactenol; Sieropresol; Solomet; Summicort; Suprametil; Urbason; Urbasone; Wyacort
Brand Mixtures: Depo-Medrol with Lidocaine (Lidocaine Hydrochloride + Methylprednisolone Acetate); Medrol Acne Lotion (Aluminum Chlorohydrate + Methylprednisolone Acetate + Sulfur); Methylprednisolone Sodium Succinate for Injection (Methylprednisolone + Water); Neo-Medrol (Methylprednisolone Acetate + Neomycin Sulfate); Neo-Medrol Acne Lotion (Aluminum Chlorohydrate + Methylprednisolone Acetate + Neomycin Sulfate + Sulfur)
PharmGKB Accession Id: PA450466

Description

A prednisolone derivative with similar anti-inflammatory action. PubChem (source: Drug Bank)

Indication

Adjunctive therapy for short-term administration in rheumatoid arthritis. (source: Drug Bank)

ATC Therapeutic Categories

  • D07AA:Corticosteroids, weak (group I)
  • D07AC:Corticosteroids, potent (group III)
  • D10AA:Corticosteroids, combinations for treatment of acne
  • H02AB:Glucocorticoids

Pharmacology, Interactions, and Contraindications

Mechanism Of Action

Unbound glucocorticoids cross cell membranes and bind with high affinity to specific cytoplasmic receptors, modifying transcription and protein synthesis. By this mechanism, glucocorticoids can inhibit leukocyte infiltration at the site of inflammation, interfere with mediators of inflammatory response, and suppress humoral immune responses. The antiinflammatory actions of corticosteroids are thought to involve phospholipase A2 inhibitory proteins, lipocortins, which control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes. (source: Drug Bank)

Pharmacology

Methylprednisolone and its derivatives, methylprednisolone sodium succinate and methylprednisolone acetate, are synthetic glucocorticoids used as antiinflammatory or immunosuppressive agents. (source: Drug Bank)

Absorption, Distribution, Metabolism, Elimination & Toxicity

Biotransformation

Hepatic (source: Drug Bank)

Protein Binding

78% (source: Drug Bank)

Absorption

Oral bioavailability 80-99% (source: Drug Bank)

Toxicity

LD<sub>50</sub>=2000 mg/kg (orally in rat) (source: Drug Bank)

Isomeric SMILES Code:

C[C@H]1C[C@H]2[C@@H]3CC[C@@]([C@]3(C[C@@H]([C@@H]2[C@@]4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O (source: Drug Bank)

The following genes are in curated knowledge about this drug.

  Gene Relationship Evidence
Phenotype data available Genotype Data Available Literature annotations available Has annotations
ABCB1
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  •   
  • PK
  • FA
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Publications

A list of non-curated publications that mention this drug along with other genes is available.

Drug Targets

Gene Description
ANXA1 Uncurated Annotation (source: Drug Bank)
NR3C1 Uncurated Annotation (source: Drug Bank)

A list of non-curated publications that mention this drug along with other drugs is available.

Non-Curated Information

A list of non-curated publications that mention this drug along with other diseases is available.

LinkOuts

Web Resource:
Wikipedia
DrugBank:
DB00959
KEGG Drug ID:
D00407
PubChem Compound ID:
6741
PubChem Substance ID:
149724

Common Searches

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Non-Curated Publications

A list of non-curated publications that mention this drug is available.

PharmGKB integrates drug information from different sources: DrugBank, Open Eye Scientific Software.
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