fisogatinib   Click here for help

GtoPdb Ligand ID: 10220

Synonyms: BLU-554 | BLU554 | CS-3008 | CS3008
Compound class: Synthetic organic
Comment: Fisogatinib (BLU-554) is an orally bioavailable, potent and highly selective fibroblast growth factor receptor 4 (FGFR4) inhibitor. It was discovered by Blueprint Medicines [1] (probably compound number 40 therein), and is being investigated for clinical anti-tumour efficacy in cancers that are driven by FGFR4 activation (for example, in liver cancers where the FGF19/FGFR4 signalling pathway is activated by genetic alteration). Structurally, fisogatinib is a derivative of BLU-9931 and is similarly an irreversible type tryosine kinase inhibitor.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 6
Hydrogen bond donors 2
Rotatable bonds 8
Topological polar surface area 94.6
Molecular weight 502.12
XLogP 4.3
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES C=CC(=O)NC1CCOCC1Nc1ncc2c(n1)ccc(c2)c1c(Cl)c(OC)cc(c1Cl)OC
Isomeric SMILES C=CC(=O)N[C@H]1CCOC[C@H]1Nc1ncc2c(n1)ccc(c2)c1c(Cl)c(OC)cc(c1Cl)OC
InChI InChI=1S/C24H24Cl2N4O4/c1-4-20(31)28-16-7-8-34-12-17(16)30-24-27-11-14-9-13(5-6-15(14)29-24)21-22(25)18(32-2)10-19(33-3)23(21)26/h4-6,9-11,16-17H,1,7-8,12H2,2-3H3,(H,28,31)(H,27,29,30)/t16-,17+/m0/s1
InChI Key MGZKYOAQVGSSGC-DLBZAZTESA-N
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Summary of Clinical Use Click here for help
ClinicalTrials.gov has one registered BLU-554 trial (as of Feb 2019) that is a first-in-human study designed to ascertain the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antineoplastic activity of BLU- 554 as an orally delivered drug in patients with advanced FGF19-positive hepatocellular carcinoma. Click here to link to ClinicalTrials.gov's full list of BLU-554 trials. In China clinical development has been licenced to CStone Pharmaceuticals, and their research code for the compound is CS3008.
Preliminary clinical data is reported, in a review of therapies that are in development for gastrointestinal cancers, by Yee (2018) [2]. This early data shows that BLU-554 produced an anti-tumour response in patients with FGF19-positive HCC (, but not in patients with FGF19-negative HCC, a result that validates the mechanism of action of BLU-554. We await peer-reviewed publication of this data.