Infigratinib phosphateProduct ingredient for Infigratinib
- Name
- Infigratinib phosphate
- Drug Entry
- Infigratinib
Infigratinib is a pan-fibroblast growth factor receptor (FGFR) kinase inhibitor. By inhibiting the FGFR pathway, which is often aberrated in cancers such as cholangiocarcinoma, infigratinib suppresses tumour growth.1 Cholangiocarcinoma is the most common primary malignancy affecting the biliary tract and the second most common primary hepatic malignancy.2 Infitratinib is a pan-FGFR inhibitor, as it is an ATP-competitive inhibitor of all four FGFR receptor subtypes.1
On May 28, 2021, the FDA granted accelerated approval to infigratinib - under the market name Truseltiq - for the treatment of previously treated, unresectable locally advanced or metastatic cholangiocarcinoma in adults with a fibroblast growth factor receptor 2 (FGFR2) fusion or another rearrangement as detected by an FDA-approved test.5 This approval follows pemigatinib, another FGFR inhibitor approved by the FDA for the same therapeutic indication.
- Accession Number
- DBSALT002096
- Structure
- Synonyms
- Not Available
- UNII
- 58BH47BV6S
- CAS Number
- 1310746-10-1
- Weight
- Average: 658.47
Monoisotopic: 657.1634389 - Chemical Formula
- C26H34Cl2N7O7P
- InChI Key
- GUQNHCGYHLSITB-UHFFFAOYSA-N
- InChI
- InChI=1S/C26H31Cl2N7O3.H3O4P/c1-5-34-10-12-35(13-11-34)18-8-6-17(7-9-18)31-21-15-22(30-16-29-21)33(2)26(36)32-25-23(27)19(37-3)14-20(38-4)24(25)28;1-5(2,3)4/h6-9,14-16H,5,10-13H2,1-4H3,(H,32,36)(H,29,30,31);(H3,1,2,3,4)
- IUPAC Name
- 3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-(6-{[4-(4-ethylpiperazin-1-yl)phenyl]amino}pyrimidin-4-yl)-1-methylurea; phosphoric acid
- SMILES
- OP(O)(O)=O.CCN1CCN(CC1)C1=CC=C(NC2=CC(=NC=N2)N(C)C(=O)NC2=C(Cl)C(OC)=CC(OC)=C2Cl)C=C1
- External Links
- ChemSpider
- 26615481
- ChEMBL
- CHEMBL1834657
- Predicted Properties
Property Value Source Water Solubility 0.0299 mg/mL ALOGPS logP 4.68 ALOGPS logP 4.78 Chemaxon logS -4.3 ALOGPS pKa (Strongest Acidic) 9.98 Chemaxon pKa (Strongest Basic) 8.23 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 8 Chemaxon Hydrogen Donor Count 2 Chemaxon Polar Surface Area 95.09 Å2 Chemaxon Rotatable Bond Count 8 Chemaxon Refractivity 152.71 m3·mol-1 Chemaxon Polarizability 58.51 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 1 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon