General
Preferred name
ETORICOXIB
Synonyms
Etoricoxib D4 ()
MK-0663 D4 ()
L-791456 D4 ()
Arcoxia ()
MK-663 ()
Tauxib ()
L-791456 ()
Nucoxia ()
DESVENLAFAXINE ()
MK-0663 ()
Arcoxia, MK-663, MK-0663, Tauxib, Algix, Nucoxia ()
P&D ID
PD009436
CAS
202409-33-4
Tags
available
drug
First approval
2002
1998
Drug indication
rheumatic disease
Rheumatoid arthritis
Drug Status
approved
investigational
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
PHARMACODYNAMICS
Etoricoxib is a COX-2 selective inhibitor (approximately 106 times more selective for COX-2 inhibition over COX-1).
MOA
Like any other COX-2 selective inhibitor Etoricoxib selectively inhibits isoform 2 of cyclo-oxigenase enzyme (COX-2), preventing production of prostaglandins (PGs) from arachidonic acid.
DESCRIPTION
Etoricoxib is a selective COX-2 inhibitor, non-steroidal anti-inflammatory (NSAID) drug.
COVID-19: Etoricoxib offers potential to be repositioned to inhibit cytokine storm in COVID-19 patients . (GtoPdb)
COVID-19: Etoricoxib offers potential to be repositioned to inhibit cytokine storm in COVID-19 patients . (GtoPdb)
PRICE
29
DESCRIPTION
Etoricoxib (MK-0663) is a non steroidal anti-inflammatory agent, acting as a selective and orally active COX-2 inhibitor, with IC50s of 1.1 ¦ÌM and 116 ¦ÌM for COX-2 and COX-1 in human whole blood.
DESCRIPTION
Etoricoxib is a COX-2 selective inhibito. Etoricoxib is a non steroidal anti-inflammatory agent, has antipyretic, analgesic, and potential antineoplastic properties.
(Enamine Bioactive Compounds)
DESCRIPTION
Etoricoxib (MK-663) is a synthetic, nonsteroidal anti-inflammatory drug (NSAID) with antipyretic, analgesic, and potential antineoplastic properties. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in inhibition of the conversion of arachidonic acid into prostaglandins. Inhibition of COX-2 may induce apoptosis and inhibit tumor cell proliferation and angiogenesis.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
25
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine Bioactive Compounds
Guide to Pharmacology
Ki Database
LSP-MoA library (Laboratory of Systems Pharmacology)
LSP-OptimalKinase library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Other bioactive compounds
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
43
Molecular Weight
358.05
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
0
Rotatable Bonds
3
Ring Count
3
Aromatic Ring Count
3
cLogP
4.18
TPSA
59.92
Fraction CSP3
0.11
Chiral centers
0.0
Largest ring
6.0
QED
0.7
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
COX
PTGS2
Pathway
Immunology/Inflammation
Neuroscience
Member status
member
MOA
Cyclooxygenase-2 Inhibitors
Non-Steroidal Antiinflammatory Drugs
cyclooxygenase inhibitor
Indication
rheumatoid arthritis, psoriatic arthritis, osteoarthritis, gout, ankylosing spondylitis
Therapeutic Class
Antiinflammatory Agents
Source data

