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Tedalinab

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Tedalinab
Identifiers
  • (4S,7R)-1-(2,4-difluorophenyl)-N-(1,1-dimethylethyl)-4,5,6,7-tetrahydro-4,7-methano-1H-indazole-3-carboxamide
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H21F2N3O
Molar mass345.394 g·mol−1
3D model (JSmol)
  • CC(C)(C)NC(=O)C1=NN(C2=C1[C@@H]3CC[C@H]2C3)C4=C(C=C(C=C4)F)F
  • InChI=1S/C19H21F2N3O/c1-19(2,3)22-18(25)16-15-10-4-5-11(8-10)17(15)24(23-16)14-7-6-12(20)9-13(14)21/h6-7,9-11H,4-5,8H2,1-3H3,(H,22,25)/t10-,11+/m0/s1
  • Key:NTPZXHMTJGOMCJ-WDEREUQCSA-N

Tedalinab (GRC-10693) is a drug developed byGlenmark Pharmaceuticals for the treatment ofosteoarthritis andneuropathic pain, which acts as a potent and selectivecannabinoidCB2receptoragonist. It has a very high selectivity of 4700x for CB2 over the relatedCB1 receptor, has good oral bioavailability and has shown promising safety results and effectiveanalgesic andantiinflammatory actions in earlyclinical trials.[1] Many related compounds are known, most of which also show high CB2 selectivity.[2]

See also

[edit]

References

[edit]
  1. ^Glenmark’s Molecule for Neuropathic Pain, Osteoarthritis - GRC 10693, Successfully Completes Phase I Trials. April 13, 2009.
  2. ^Glenmark Pharmaceuticals. NOVEL CANNABINOID RECEPTOR LIGANDS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND PROCESS FOR THEIR PREPARATION, Filed June 1st, 2006. WO 2006/129178.
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