Infigratinib phosphate NEW
| Price | $40 | $56 | $77 |
| Package | 5mg | 10mg | 25mg |
| Supply Ability: | 10g |
| Update Time: | 2026-05-11 |
Product Details
| Product Name: Infigratinib phosphate | CAS No.: 1310746-10-1 |
| Purity: 99.24% | Supply Ability: 10g |
| Release date: 2026/05/11 |
Product Introduction
Bioactivity
| Name | Infigratinib phosphate |
| Description | Infigratinib phosphate (BGJ-398 phosphate) is an effective inhibitor of the FGFR family (IC50: 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively). |
| In vitro | Infigratinib inhibits the proliferation of the FGFR1-, FGFR2-, and FGFR3-dependent BaF3 cells with IC50 values which are in the low nanomolar range and comparable to those observed for the inhibition of the receptors kinase activity in the enzymatic assay. Infigratinib phosphate suppresses FGFR1, FGFR2, and FGFR3(IC50=~1 nM), FGFR3K650E(IC50=4.9 nM), and FGFR4(IC50=60 nM). IC50 values for all other kinases are in the μM range (FYN, LCK, YES, and ABL, IC50=1.9, 2.5, 1.1, and 2.3 μM, respectively) except for VEGFR2, KIT, and LYN, which are inhibited at submicromolar concentrations (IC50=0.18, 0.75, and 0.3 μM, respectively). Infigratinib (ranging between 1 nM and 10 μM) is effective at inhibiting cell growth of FGFR2-mutant endometrial cancer cells. For the remaining cells, all IC50 values are greater than 1.5 μM except for VEGFR2 (IC50 1449 and 938 nM), for which there is at least a 400-fold selectivity versus FGFR1, FGFR2, and FGFR3[1][2]. |
| In vivo | Infigratinib, at a dosage of 30 mg/kg, effectively inhibits the proliferation of FGFR2-mutated endometrial cancer in xenograft models using athymic nude mice. The compound is administered either as a 5 mg/kg intravenous injection in NMP/PEG200 (1:9, v/v) or orally at 20 mg/kg in a PEG300/D5W (2:1, v/v) mixture. Following intravenous administration, Infigratinib quickly disperses from the bloodstream to peripheral tissues, evidenced by a high distribution volume (26 L/kg). Pharmacokinetic studies reveal that its oral bioavailability is 32%, with a significant plasma clearance rate of 3.3 L/h/kg, approximately 61% of liver blood flow. The drug concentration in tumors relative to plasma, based on the Area Under the Curve (AUC) ratio, is 10 after oral administration, indicating significant efficacy in targeting tumor cells. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO : 11.7 mg/mL (17.77 mM), Sonication is recommended. |
| Keywords | NVP-BGJ-398 Phosphate | NVP-BGJ398 Phosphate | NVP-BGJ 398 Phosphate | Infigratinib Phosphate | FGFR4 | FGFR3 | FGFR2 | FGFR1 | BGJ-398 Phosphate | BGJ398 Phosphate | BGJ 398 Phosphate |
| Inhibitors Related | Amlexanox | Regorafenib monohydrate | Nintedanib | Ferulic Acid | Nintedanib esylate | Regorafenib | Pemigatinib | Formononetin | Lenvatinib mesylate | Erdafitinib | Lenvatinib | Pazopanib |
| Related Compound Libraries | Failed Clinical Trials Compound Library | Bioactive Compound Library | Membrane Protein-targeted Compound Library | Kinase Inhibitor Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Anti-Cancer Approved Drug Library | FDA-Approved Drug Library | FDA-Approved Kinase Inhibitor Library | Bioactive Compounds Library Max | Anti-Cancer Active Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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