Catequentinib

Catequentinib
Clinical data
Trade names	Focus V
Other names	Anlotinib; AL3818; AL-3818
Identifiers
	IUPAC name 1-[[4-[(4-Fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinolin-7-yl]oxymethyl]cyclopropan-1-amine;
CAS Number	1058156-90-3 ;
PubChem CID	25017411 ;
DrugBank	DB11885 ;
UNII	GKF8S4C432 ;
KEGG	D12526 ;
ChEMBL	ChEMBL4303201 ;
Chemical and physical data
Formula	C23H22FN3O3
Molar mass	407.445 g·mol−1
3D model (JSmol)	Interactive image ;
	SMILES CC1=CC2=C(N1)C=CC(=C2F)OC3=C4C=C(C(=CC4=NC=C3)OCC5(CC5)N)OC;
	InChI InChI=InChI=1S/C23H22FN3O3/c1-13-9-15-16(27-13)3-4-19(22(15)24)30-18-5-8-26-17-11-21(20(28-2)10-14(17)18)29-12-23(25)6-7-23/h3-5,8-11,27H,6-7,12,25H2,1-2H3; Key:KSMZEXLVHXZPEF-UHFFFAOYSA-N;

Last updated February 25, 2025

Catequentinib (INN; formerly anlotinib) is a pharmaceutical drug for the treatment of cancer. It is approved in China for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) in patients who have undergone progression or recurrence after at least two lines of systemic chemotherapy.^[1] It is also approved in China as a second‑line treatment for advanced soft-tissue sarcoma.^[2]

Catequentinib is a tyrosine kinase inhibitor that targets several different proteins including vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR), platelet-derived growth factor receptors (PDGFR), and c-kit.^[3]

Adverse effects include hypertension, fatigue, thyroid-stimulating hormone elevation, and hand-foot syndrome, among others.^[4]

References

↑ Syed YY (July 2018). "Anlotinib: First Global Approval". Drugs. 78 (10): 1057–1062. doi:10.1007/s40265-018-0939-x. PMID 29943374.
↑ Gao Y, Liu P, Shi R (August 2020). "Anlotinib as a molecular targeted therapy for tumors". Oncology Letters. 20 (2): 1001–1014. doi:10.3892/ol.2020.11685. PMC 7377159 . PMID 32724339.
↑ Shen G, Zheng F, Ren D, Du F, Dong Q, Wang Z, et al. (September 2018). "Anlotinib: a novel multi-targeting tyrosine kinase inhibitor in clinical development". Journal of Hematology & Oncology. 11 (1): 120. doi: 10.1186/s13045-018-0664-7 . PMC 6146601 . PMID 30231931.
↑ Li S, Wang H (2023). "Research Progress on Mechanism and Management of Adverse Drug Reactions of Anlotinib". Drug Design, Development and Therapy. 17: 3429–3437. doi: 10.2147/DDDT.S426898 . PMC 10657757 . PMID 38024530.

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[1] Syed YY (July 2018). "Anlotinib: First Global Approval". Drugs. 78 (10): 1057–1062. doi:10.1007/s40265-018-0939-x. PMID 29943374.

[2] Gao Y, Liu P, Shi R (August 2020). "Anlotinib as a molecular targeted therapy for tumors". Oncology Letters. 20 (2): 1001–1014. doi:10.3892/ol.2020.11685. PMC 7377159 . PMID 32724339.

[3] Shen G, Zheng F, Ren D, Du F, Dong Q, Wang Z, et al. (September 2018). "Anlotinib: a novel multi-targeting tyrosine kinase inhibitor in clinical development". Journal of Hematology & Oncology. 11 (1): 120. doi: 10.1186/s13045-018-0664-7 . PMC 6146601 . PMID 30231931.

[4] Li S, Wang H (2023). "Research Progress on Mechanism and Management of Adverse Drug Reactions of Anlotinib". Drug Design, Development and Therapy. 17: 3429–3437. doi: 10.2147/DDDT.S426898 . PMC 10657757 . PMID 38024530.

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