Galunisertib

Chemical compound
Galunisertib
Clinical data
Routes of
administration		PO
Identifiers
  • 4-(5,6-Dihydro-2-(6-methyl-2-pyridinyl)-4H-pyrrolo(1,2-b)pyrazol-3-yl)-6-quinolinecarboxamide
CAS Number
  • 700874-72-2
PubChem CID
  • 10090485
ChemSpider
  • 8266022
UNII
  • 3OKH1W5LZE
KEGG
  • D10437
ChEBI
  • CHEBI:137064
CompTox Dashboard (EPA)
  • DTXSID00220362 Edit this at Wikidata
Chemical and physical data
FormulaC22H19N5O
Molar mass369.428 g·mol−1
3D model (JSmol)
  • Interactive image
  • N1=CC=C(C2=CC(=CC=C12)C(=O)N)C1=C2N(N=C1C1C=CC=C(N=1)C)CCC2
InChI
  • InChI=1S/C22H19N5O/c1-13-4-2-5-18(25-13)21-20(19-6-3-11-27(19)26-21)15-9-10-24-17-8-7-14(22(23)28)12-16(15)17/h2,4-5,7-10,12H,3,6,11H2,1H3,(H2,23,28)
  • Key:IVRXNBXKWIJUQB-UHFFFAOYSA-N

Galunisertib (LY2157299) is a small molecular experimental cancer drug previously in development by Eli Lilly. It is a TGF-b inhibitor.[1] Development of galunisertib by Eli Lilly was discontinued in January 2020.[2]

Galunisertib was investigated in a phase II trial for treatment of hepatocellular carcinoma.[3] Pre-clinically, combination of galunisertib with PD-L1 blockade resulted in improved tumor growth inhibition.[4]

References

  1. ^ "Lilly Oncology Pipeline - Lilly USA". www.lillyoncologypipeline.com.
  2. ^ "Eli Lilly cuts 3 cancer drugs amid Q4 clear-out".
  3. ^ Clinical trial number NCT01246986 for "A Study of LY2157299 in Participants With Hepatocellular Carcinoma" at ClinicalTrials.gov
  4. ^ Holmgaard RB, Schaer DA, Li Y, Castaneda SP, Murphy MY, Xu X, Inigo I, Dobkin J, Manro JR, Iversen PW, Surguladze D, Hall GE, Novosiadly RD, Benhadji KA, Plowman GD, Kalos M, Driscoll KE (June 2018). "Targeting the TGFβ pathway with galunisertib, a TGFβRI small molecule inhibitor, promotes anti-tumor immunity leading to durable, complete responses, as monotherapy and in combination with checkpoint blockade". Journal for Immunotherapy of Cancer. 6 (1): 47. doi:10.1186/s40425-018-0356-4. PMC 5987416. PMID 29866156.