Treatment | Dose | IC50 and target | Clinical trial phase, ClinicalTrials.gov identifier | Supplier, catalogue number | References |
---|---|---|---|---|---|
DMSO (vehicle control) | Equal to DMSO in drug treatments (≥ 1/5000) | NA | NA | Thermo-Fisher, D12345 |  |
BGJ398/ Infigratinib (FGFRi) | 125, 250, 500, 1000 and 2500 nM | IC50 – FGFR1–3: 0.9–1.4 nM, FGFR4: 60 nM | Phase II, NCT02150967 | SelleckChem, S2183 | [31] |
PD0325901/ Mirdametinib (MEKi) | 125, 250, 500 and 1000 nM | IC50 – MEK: 0.33 nM | Phase II, NCT03962543 | SelleckChem, S1036 or MedChem Express, HY-10254 | [32] |
PH-797804 (p38i) | 500 nM | IC50 – p38α: 26 nM; p38β 102 nM | Phase II, NCT00559910 | MedChem Express, HY-10403 | [33] |
GSK1059615 (PI3Ki) | 500 nM | IC50 – PI3Kα/ β/δ/γ: 0.4–5 nM, mTOR: 12 nM | Phase I, NCT00695448 | MedChem Express, HY-12036 |  |
Recombinant mouse FGF9 | 50Â ng/mL | FGFR1-3 | NA | R&D systems, 7399-F9-025 | [20] |
AZD4547 (second FGFR inhibitor) | 125, 250 and 500 nM | IC50 – FGFR1-3: 0.2–2.5 nM; FGFR4: 165 nM; VEGFR2: 24 nM | Phase II, NCT02465060 | SelleckChem, S2801 | [34] |
SU5402 (third FGFR inhibitor) | 5000Â nM | IC50 VEGFR: 20Â nM; FGFR1: 30Â nM | N/A | MedChem Express, HY-10407 | [35] |
Ralimetinib dimesylate/ LY2228820 (second p38 inhibitor) | 500 nM | IC50 – p38α: 5.3 nM; p38β: 5.3 nM | Phase I, NCT01663857 | MedChem Express, HY-13241 | [36] |
PF-04691502 (second PI3K inhibitor) | 500 nM | IC50 – PI3Kα/ β/δ/γ: 1.6–2.1 nM; mTOR: 16 nM | Phase II, NCT01420081 | MedChem Express, HY-15177 | [37] |