Repositioning Candidate Details

Candidate ID: R0340
Source ID: DB00939
Source Type: approved; vet_approved
Compound Type: small molecule
Compound Name: Meclofenamic acid
Synonyms: Meclofenamate; Meclofenamic acid; N-(2,6-dichloro-3-methylphenyl)anthranilic acid; N-(2,6-dichloro-m-tolyl)anthranilic acid; N-(3-methyl-2,6-dichlorophenyl)anthranilic acid
Molecular Formula: C14H11Cl2NO2
SMILES: CC1=C(Cl)C(NC2=CC=CC=C2C(O)=O)=C(Cl)C=C1
Structure:
DrugBank Description: A non-steroidal anti-inflammatory agent with antipyretic and antigranulation activities. It also inhibits prostaglandin biosynthesis.
CAS Number: 644-62-2
Molecular Weight: 296.149
DrugBank Indication: For the relief of mild to moderate pain, for the treatment of primary dysmenorrhea and for the treatment of idiopathic heavy menstrual blood loss. Also for relief of the signs and symptoms of acute and chronic rheumatoid arthritis and osteoarthritis.
DrugBank Pharmacology: Meclofenamic acid is a nonsteroidal agent which has demonstrated anti-inflammatory, analgesic, and antipyretic activity in laboratory animals.
DrugBank MoA: The mode of action, like that of other nonsteroidal anti-inflammatory agents, is not known. Therapeutic action does not result from pituitary-adrenal stimulation. In animal studies, meclofenamic acid was found to inhibit prostaglandin synthesis and to compete for binding at the prostaglandin receptor site. In vitro meclofenamic acid was found to be an inhibitor of human leukocyte 5-lipoxygenase activity. These properties may be responsible for the anti-inflammatory action of meclofenamic acid. There is no evidence that meclofenamic acid alters the course of the underlying disease.
Targets: Prostaglandin G/H synthase 1 inhibitor; Prostaglandin G/H synthase 2 inhibitor; Arachidonate 5-lipoxygenase inhibitor; Potassium voltage-gated channel subfamily KQT member 2 other; Potassium voltage-gated channel subfamily KQT member 3 other
Inclusion Criteria: Therapeutic strategy associated