Galunisertib

Galunisertib
Clinical data
Routes of; administration	PO
Identifiers
	IUPAC name 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 ;
Chemical and physical data
Formula	C22H19N5O
Molar mass	369.428 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES 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

^ "Lilly Oncology Pipeline - Lilly USA". www.lillyoncologypipeline.com.
^ "Eli Lilly cuts 3 cancer drugs amid Q4 clear-out".
^ Clinical trial number NCT01246986 for "A Study of LY2157299 in Participants With Hepatocellular Carcinoma" at ClinicalTrials.gov
^ 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.

[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

[pmid29866156-4] 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.

[1]

[2]

[3]

[4]

Clinical data

Routes of administration	PO
Identifiers
IUPAC name 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
Chemical and physical data
Formula	C₂₂H₁₉N₅O
Molar mass	369.428 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES 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

References

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