Glafenine
A pain-relieving medication used to treat mild to moderate pain. It belongs to the NSAID class of drugs and works by reducing inflammation and blocking pain signals.
Peso Molecular
372,8000 g/mol
LogP
3,50
TPSA
91,70 Ų
Regra dos 5 de Lipinski
Aprovado
Mecanismo de Ação
Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.
Estrutura 2D
Cite this structure
Embed this structure
SMILES
O=C(OCC(O)CO)c1ccccc1Nc1ccnc2cc(Cl)ccc12
InChI
InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)
Molecular Formula
C19H17ClN2O4
HBD / HBA
3 / 6
Ligações Rotacionáveis
7
Átomos Pesados
26
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
A pain-relieving medication used to treat mild to moderate pain. It belongs to the NSAID class of drugs and works by reducing inflammation and blocking pain signals.
Inhibits cyclooxygenase (COX-1 and/or COX-2) enzymes, reducing the synthesis of prostaglandins and thromboxanes from arachidonic acid. This produces anti-inflammatory, analgesic, and antipyretic effects.
Yes, Glafenine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL146095. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3474. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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