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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T60185 | FGFR2-IN-3 | FGFR | |
FGFR2-IN-3 is an orally active selective FGFR2 inhibitor[1]. | |||
T63850 | FGFR2-IN-3 hydrochloride | ||
FGFR2-IN-3 hydrochloride is a selective, orally active FGFR2 inhibitor. | |||
T5044 | Futibatinib | TAS120,FGFR-IN-1 | FGFR |
Futibatinib (FGFR-IN-1) is a novel, potent and highly selective FGFR inhibitor, used for antitumor treatment. | |||
T1948 | AZD4547 | VEGFR , FGFR | |
AZD4547, a new-type specific FGFR inhibitor, targets for FGFR1/2/3 (IC50: 0.2/2.5/1.8 nM in cell-free assays). | |||
T2638 | Gandotinib | LY2784544 | VEGFR , FGFR , FLT , JAK |
LY2784544(Gandotinib (LY2784544)) is a potent JAK2 inhibitor (IC50: 3 nM), effective in JAK2V617F(Ki: 0.245 nM). The selectivity is higher 8- and 20-fold than JAK1 and JAK3. | |||
T73146 | FGFR3-IN-5 | ||
FGFR3-IN-5 is a potent, selective FGFR3 inhibitor, exhibiting IC50 values of 3 nM (FGFR3), 44 nM (FGFR2), and 289 nM (FGFR1), respectively. This compound is utilized in cancer research. | |||
T3512 | S49076 HCl | S-49076 Hydrochloride | FGFR , c-Met/HGFR , TAM Receptor |
S49076 HCl (S-49076 Hydrochloride) is an effective inhibitor of MET, AXL/MER, and FGFR1/2/3. S49076 HCl potently blocked cellular phosphorylation of MET, AXL, and FGFRs and inhibited downstream signaling in vitro and in ... |