Date published: 2026-4-6

1-800-457-3801

SCBT Portrait Logo
Seach Input

FRMD6 Activators

SEE ALSO...

Items 1 to 10 of 19 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

ROCK inhibitor, affecting the Hippo pathway and FRMD6.

Verteporfin

129497-78-5sc-475698
sc-475698A
10 mg
100 mg
$354.00
$2764.00
5
(0)

Disrupts YAP-TEAD interaction, affecting FRMD6 activity.

GSK 269962

850664-21-0sc-363279
sc-363279A
10 mg
50 mg
$300.00
$1000.00
1
(0)

GSK269962A inhibits FRMD6 through its interaction with the FRMD6 kinase domain, disrupting its binding to substrates and impeding cell migration and invasion.

Doxorubicin

23214-92-8sc-280681
sc-280681A
1 mg
5 mg
$176.00
$426.00
43
(3)

Affects the Hippo pathway through DNA intercalation.

H-1152 dihydrochloride

451462-58-1sc-203592
sc-203592A
1 mg
5 mg
$104.00
$364.00
7
(1)

H-1152 is another Rho kinase inhibitor that indirectly affects FRMD6 by modulating the Rho/ROCK pathway, leading to reduced FRMD6-mediated cell adhesion and migration.

Lysophosphatidic Acid

325465-93-8sc-201053
sc-201053A
5 mg
25 mg
$98.00
$341.00
50
(3)

Modulates Hippo signaling through G-protein-coupled receptor signaling.

RKI-1447

1342278-01-6sc-472590
1 mg
$330.00
(0)

RKI-1447 is a potent inhibitor of the PAK4 kinase, which phosphorylates and activates FRMD6. Inhibiting PAK4 reduces FRMD6 activity, impairing cell migration and metastasis.

PF-562271

717907-75-0sc-478488
sc-478488A
sc-478488B
5 mg
10 mg
50 mg
$312.00
$474.00
$1124.00
3
(1)

PF-562271 targets the FAK kinase, which can interact with FRMD6 in focal adhesions. Inhibiting FAK disrupts FRMD6's role in cell adhesion and migration processes.

Lovastatin

75330-75-5sc-200850
sc-200850A
sc-200850B
5 mg
25 mg
100 mg
$29.00
$90.00
$339.00
12
(1)

Inhibits HMG-CoA reductase, influencing Hippo signaling.

CCG-1423

285986-88-1sc-205241
sc-205241A
1 mg
5 mg
$30.00
$90.00
8
(1)

CCG-1423 inhibits the interaction between FRMD6 and its downstream target Cdc42, impairing the formation of actin-based structures crucial for cell migration and invasion.