LGK974

Pharmaceutical compound From Wikipedia, the free encyclopedia

LGK974 (WNT974) is an experimental drug which acts as an inhibitor of the porcupine O-acyltransferase enzyme, which plays an important part in the growth of certain types of cancer, especially colorectal cancer, pancreatic cancer, hepatocellular carcinoma and head and neck cancers. It is in early stage clinical trials for a number of cancer types.[1][2][3]

CAS Number
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LGK974
Identifiers
  • 2-[5-methyl-6-(2-methylpyridin-4-yl)pyridin-3-yl]-N-(5-pyrazin-2-ylpyridin-2-yl)acetamide
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
PDB ligand
Chemical and physical data
FormulaC23H20N6O
Molar mass396.454 g·mol−1
3D model (JSmol)
  • CC1=CC(=CN=C1C2=CC(=NC=C2)C)CC(=O)NC3=NC=C(C=C3)C4=NC=CN=C4
  • InChI=1S/C23H20N6O/c1-15-9-17(12-28-23(15)18-5-6-25-16(2)10-18)11-22(30)29-21-4-3-19(13-27-21)20-14-24-7-8-26-20/h3-10,12-14H,11H2,1-2H3,(H,27,29,30)
  • Key:XXYGTCZJJLTAGH-UHFFFAOYSA-N
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LGK974 has recently shown promise in preclinical models of the ultra-rare disease sclerosteosis, providing an alternative to invasive surgeries commonly required to the management of pathologies.[4]

References

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