Date published: 2025-12-24

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FAM55C Inhibitors

FAM55C inhibitors encompass a range of chemical compounds that indirectly lead to the downregulation of FAM55C activity by targeting specific signaling pathways and cellular processes. The MEK inhibitors PD 98059 and U0126 are prime examples, as they disrupt the MEK/ERK signaling cascade, which could be crucial for FAM55C's role in cellular functions that rely on ERK activity. Similarly, LY 294002 and Wortmannin, both PI3K inhibitors, impede the PI3K/AKT pathway, leading to reduced AKT phosphorylation, which may in turn diminish FAM55C activity if it is regulated by this pathway. Rapamycin, targeting the mTORC1 pathway, could suppress FAM55C function by throttling protein synthesis and growth signaling if FAM55C is intertwined with mTOR's regulatory network. The p38 MAPK inhibitor SB 203580 potentially reduces FAM55C activity through the attenuation of p38-mediated stress and inflammatory signaling, which FAM55C may be a part of. SP600125, by inhibiting JNK, might result in the downregulation of FAM55C if its activity is linked to JNK-dependent processes. The inhibition spectrum of FAM55C extends to compounds affecting other regulatory nodes in cellular signaling. Y-27632's inhibition of ROCK could diminish FAM55C function by disrupting cytoskeletal organization and cell motility, implicating a role for FAM55C in these structural processes. GW 5074, a Raf-1 kinase inhibitor could decrease FAM55C activity by impairing the Raf/MEK/ERK pathway, suggesting a dependency of FAM55C on signals emanating from Raf kinase activity. The role of FAM55C in differentiation pathways is highlighted by BML-275, which inhibits BMP signaling; if FAM55C is involved in BMP-mediated cellular differentiation, its activity would be reduced by BML-275. Each of these inhibitors, through their targeted biochemical interactions, contributes to the collective mechanism of downregulating FAM55C without directly altering its expression or requiring direct inhibition of the protein itself.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$39.00
$90.00
212
(2)

PD 98059 is a selective MEK inhibitor that indirectly diminishes FAM55C's function by inhibiting the MEK/ERK pathway. Since FAM55C is involved in cellular processes regulated by this pathway, the inhibition of MEK leads to decreased ERK activation, which in turn can reduce the functional activity of FAM55C as it may be downstream or modulated by ERK signaling.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

LY 294002 is a phosphoinositide 3-kinase (PI3K) inhibitor that decreases the activity of the PI3K/AKT pathway. By inhibiting PI3K, LY 294002 reduces AKT phosphorylation and activity, which could lead to reduced function of FAM55C if it is regulated by or associated with the PI3K/AKT pathway, a common regulator of cellular growth and survival.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

Rapamycin is an mTOR inhibitor that blocks the mTORC1 pathway, leading to a decrease in protein synthesis and cell growth. If FAM55C activity is linked to mTOR signaling, as it often is with proteins involved in cell growth, rapamycin inhibition of mTOR could lead to diminished activity of FAM55C through reduced cellular capacity for protein production and growth signaling.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$88.00
$342.00
284
(5)

SB 203580 is a p38 MAPK inhibitor that blocks p38 mediated signaling. By inhibiting p38 MAPK, this compound can lead to reduced inflammatory responses and stress responses in cells. If FAM55C is involved in pathways that are modulated by p38 MAPK, such as stress or inflammatory signaling, inhibition by SB 203580 would likely result in decreased functional activity of FAM55C.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$63.00
$241.00
136
(2)

U0126 is a selective inhibitor of MEK1/2, which prevents the activation of ERK1/2. This inhibition may lead to a decrease in the functional activity of FAM55C if it operates within or is modulated by the MEK/ERK pathway, as U0126 would reduce the downstream signaling events that could be essential for FAM55C's function.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

SP600125 is an inhibitor of c-Jun N-terminal kinase (JNK), which is involved in regulatory processes such as apoptosis and cell differentiation. By inhibiting JNK, SP600125 could decrease the functional activity of FAM55C if it is regulated by or involved in pathways that are dependent on JNK signaling.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$66.00
$219.00
$417.00
97
(3)

Wortmannin is a potent and irreversible inhibitor of PI3K. Inhibiting PI3K with Wortmannin could lead to diminished AKT signaling and potentially decrease the functional activity of FAM55C if it is associated with or regulated by the PI3K/AKT pathway.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$182.00
$693.00
88
(1)

Y-27632 is an inhibitor of Rho-associated protein kinase (ROCK), which plays a significant role in cell motility and structure. By inhibiting ROCK, Y-27632 can affect cytoskeletal organization and cellular tension. If FAM55C's function is linked to cell structure or motility, inhibition of ROCK may lead to decreased functional activity of FAM55C via these cellular processes.

GW 5074

220904-83-6sc-200639
sc-200639A
5 mg
25 mg
$106.00
$417.00
10
(1)

GW 5074 is an inhibitor of Raf-1 kinase, part of the MAPK/ERK pathway. By inhibiting Raf-1, GW 5074 can lead to reduced ERK signaling and potentially diminish the functional activity of FAM55C if FAM55C's function is modulated by or dependent on the Raf/MEK/ERK pathway.

BML-275

866405-64-3sc-200689
sc-200689A
5 mg
25 mg
$94.00
$348.00
69
(1)

BML-275 is an inhibitor of BMP signaling which acts by inhibiting the BMP type I receptors ALK2, ALK3, and ALK6. By inhibiting BMP signaling, BML-275 can affect various cellular differentiation processes. If FAM55C's function is associated with BMP pathway-mediated differentiation, inhibition by BML-275 could lead to decreased functional activity of FAM55C.