Date published: 2026-5-9

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FTS Activators

FTS activators constitute a class of chemicals that modulate the activity of the protein FTS, also known as Ras-related protein Rab-24 (Rab24), which is involved in intracellular trafficking. The exact function of Rab24 is less characterized compared to other members of the Rab family, but it is believed to play a role in vesicle trafficking, autophagy, and possibly the unconventional secretion pathway.

The activation of FTS by chemicals can be achieved through direct or indirect mechanisms. Direct FTS activators would interact with the protein itself, potentially binding to specific regions that trigger a change in its conformation, thus enhancing its natural GTPase activity or its ability to interact with other proteins involved in vesicular transport. This direct binding could also stabilize the active form of Rab24, prolonging its activity within the cell. Indirect activators of FTS might work by influencing the cellular pathways that regulate Rab24's function. These could include the upregulation of Rab24 expression, leading to an increased concentration of the protein in the cell, or the modulation of the Rab24 gene at the transcriptional level. Additionally, indirect activators may affect the post-translational modifications of Rab24, such as prenylation, which is crucial for its proper localization and function.

In a research context, FTS activators provide a means to study the biological role and the regulation of Rab24 in cells. By applying these activators, scientists can investigate how Rab24 contributes to vesicle trafficking pathways and autophagy processes. Understanding the mechanism of action of FTS activators also allows for the exploration of the broader Rab GTPase family's role in cellular dynamics and organelle biogenesis. The insights gained from such research can enhance our comprehension of the fundamental aspects of cell biology, such as how cells maintain their internal organization and respond to various stimuli through intracellular transport mechanisms.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Wortmannin is a potent and irreversible inhibitor of phosphoinositide 3-kinases (PI3K). The inhibition of PI3K prevents the phosphorylation of AKT, a key downstream effector of PI3K. As FTS is known to interact with AKT, the inhibition of AKT phosphorylation by wortmannin can lead to an increase in FTS activity.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

LY294002 is another potent inhibitor of PI3K. Similar to wortmannin, the inhibition of PI3K by LY294002 can prevent the phosphorylation of AKT, thus enhancing the activity of FTS.

Triciribine

35943-35-2sc-200661
sc-200661A
1 mg
5 mg
$104.00
$141.00
14
(1)

Triciribine specifically inhibits AKT activation by blocking its phosphorylation. The inhibition of AKT activation by triciribine can lead to an increase in the functional activity of FTS.

MK-2206 dihydrochloride

1032350-13-2sc-364537
sc-364537A
5 mg
10 mg
$182.00
$332.00
67
(1)

MK-2206 is an allosteric inhibitor that selectively inhibits AKT phosphorylation and activation. The inhibition of AKT by MK-2206 can enhance the functional activity of FTS.

Perifosine

157716-52-4sc-364571
sc-364571A
5 mg
10 mg
$188.00
$327.00
1
(2)

Perifosine is an alkylphospholipid that inhibits AKT activation. The inhibition of AKT activation by perifosine can lead to an increase in the functional activity of FTS.

A-443654

552325-16-3sc-507339
1 mg
$140.00
(0)

A-443654 is a potent and selective inhibitor of AKT that can prevent its phosphorylation. The inhibition of AKT by A-443654 can enhance the functional activity of FTS.

GSK 690693

937174-76-0sc-363280
sc-363280A
10 mg
50 mg
$255.00
$1071.00
4
(1)

GSK690693 is a pan-AKT kinase inhibitor. By inhibiting the activation of AKT, GSK690693 can enhance the functional activity of FTS.

Miltefosine

58066-85-6sc-203135
50 mg
$81.00
8
(1)

Miltefosine is an alkylphospholipid that inhibits AKT activation. The inhibition of AKT activation by miltefosine can lead to an increase in the functional activity of FTS.

AZD5363

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

AZD5363 is a potent inhibitor of all three AKT isoforms. By inhibiting AKT, AZD5363 can enhance the functional activity of FTS.