Date published: 2026-5-30

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Fibroblast Growth Factor (FGF) Inhibitors

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

AP 24534

943319-70-8sc-362710
sc-362710A
10 mg
50 mg
$175.00
$983.00
2
(1)

AP 24534 inhibits FGF-6 signaling by directly targeting and inhibiting the activity of multiple tyrosine kinases, including BCR-ABL and FGFRs, which are crucial for FGF-6 mediated cellular processes. This inhibition disrupts the phosphorylation cascade essential for FGF-6 signal transduction, leading to impaired cellular proliferation and differentiation associated with FGF-6 pathways.

PD173074

219580-11-7sc-202610
sc-202610A
sc-202610B
1 mg
5 mg
50 mg
$47.00
$143.00
$680.00
16
(1)

PD173074 is a potent and selective FGFR inhibitor that directly targets the tyrosine kinase domain, preventing autophosphorylation and downstream signaling.

SU 5402

215543-92-3sc-204308
sc-204308A
1 mg
5 mg
$63.00
$98.00
36
(3)

SU5402 is a small molecule inhibitor of FGFR tyrosine kinase activity. It interferes with the ATP-binding site of FGFR, preventing autophosphorylation and downstream signaling.

AZD4547

1035270-39-3sc-364421
sc-364421A
5 mg
10 mg
$198.00
$309.00
6
(1)

AZD4547 is a selective FGFR inhibitor that hinders FGFR autophosphorylation and downstream signaling. By targeting the kinase domain, AZD4547 directly inhibits FGFR, disrupting FGF-mediated cellular processes including proliferation and angiogenesis.

BGJ398

872511-34-7sc-364430
sc-364430A
sc-364430B
sc-364430C
5 mg
10 mg
50 mg
100 mg
$216.00
$252.00
$594.00
$1009.00
4
(1)

BGJ398 is an active inhibitor of FGFR tyrosine kinases. By binding to the ATP-binding pocket of FGFR, it prevents autophosphorylation and downstream signaling. BGJ398 directly inhibits FGFR, disrupting FGF-mediated pathways and cellular responses related to cell proliferation and angiogenesis.

Lenvatinib

417716-92-8sc-488530
sc-488530A
sc-488530B
5 mg
25 mg
100 mg
$182.00
$661.00
$1690.00
3
(0)

Lenvatinib acts as a potent inhibitor of FGF-6 through its multi-targeted action on vascular endothelial growth factor receptors (VEGFRs), platelet-derived growth factor receptors (PDGFRs), and fibroblast growth factor receptors (FGFRs), including those involved in FGF-6 signaling.

AZD5363

1143532-39-1sc-503190
5 mg
$309.00
(0)

JNJ-42756493 is a potent and selective FGFR inhibitor that interferes with the tyrosine kinase domain, preventing autophosphorylation and downstream signaling. By directly inhibiting FGFR, JNJ-42756493 disrupts FGF-mediated pathways, influencing cellular processes such as proliferation and angiogenesis.

JNJ-26481585

875320-29-9sc-364515
sc-364515A
5 mg
50 mg
$321.00
$1224.00
(1)

JNJ-26481585 is an active inhibitor of FGFR tyrosine kinase activity. By binding to the ATP-binding site, it inhibits autophosphorylation and downstream signaling. JNJ-26481585 directly targets FGFR, disrupting FGF-mediated pathways and cellular responses related to cell growth and angiogenesis.