Repositioning Candidate Details

Candidate ID: R0614
Source ID: DB04725
Source Type: investigational
Compound Type: small molecule
Compound Name: Licofelone
Synonyms: Licofelone
Molecular Formula: C23H22ClNO2
SMILES: CC1(C)CN2C(CC(O)=O)=C(C(=C2C1)C1=CC=CC=C1)C1=CC=C(Cl)C=C1
Structure:
DrugBank Description: Developed by the German pharmaceutical company, Merckle GmbH, together with EuroAlliance partners Alfa Wassermann and Lacer, licofelone (ML3000) is a dual COX/LOX inhibitor and the first member of this new class of analgesic and anti-inflammatory drugs. It is currently under evaluation as a treatment for osteoarthritis (OA), the most common form of arthritis. Although phase III trials have been successfully completed in OA patients no dates for regulatory submission have yet been given.
CAS Number: 156897-06-2
Molecular Weight: 379.879
DrugBank Indication: For the management of osteoarthritis.
DrugBank Pharmacology: Licofelone belongs to a novel class of dual-acting anti-inflammatory drugs called COX/LO inhibitors. This group of drugs simultaneously inhibits the enzymes cyclooxygenase (COX) and 5-lipoxygenase (LO).
DrugBank MoA: Licofelone, through combined 5-LOX/COX-inhibition, reduces levels of inflammatory prostaglandins and leukotrienes.
Targets: Group IIE secretory phospholipase A2; Prostaglandin G/H synthase 2; Arachidonate 5-lipoxygenase
Inclusion Criteria: Therapeutic strategy associated