Date published: 2026-4-1

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C1orf185 Inhibitors

C1orf185 inhibitors encompass an array of chemical compounds that exert their effects by interfering with various cellular signaling pathways, ultimately leading to the diminished functional activity of C1orf185. Compounds like Wortmannin and LY 294002 target the PI3K/AKT pathway, a signaling route that, when inhibited, results in reduced proliferation and survival signals that could otherwise enhance C1orf185 function. Similarly, Rapamycin's action on mTORC1 and the subsequent decrease in protein synthesis and cell growth may indirectly reduce the demand for C1orf185's activity. Inhibitors such as SB 203580 and U0126 act on the MAPK pathway by specifically targeting p38 and MEK1/2, respectively, potentially curtailing the activity of C1orf185 if it is modulated by this pathway. Additionally, the suppression of JNK by SP600125 could alter transcriptional activity, leading to a reduction in C1orf185 activity if it is under the regulatory influence of JNK-mediated signaling. Furthermore, NSC 23766 and Y-27632 manipulate the actin cytoskeleton dynamics and cellular structure by impeding Rac1 and ROCK, respectively, which could lead to a decrease in C1orf185 activity, assuming it is associated with these processes.

The specificity of C1orf185 inhibitors extends to targeting tyrosine kinase signaling, as seen with PP 1, which inhibits Src family kinases, potentially attenuating C1orf185 activity if it is involved in pathways regulated by Src kinases. JWH 073, by inhibiting Raf kinase, could also diminish MAPK/ERK signaling, affecting C1orf185 activity if it falls within this signaling cascade. PD 98059, a MEK inhibitor, may decrease ERK pathway signaling, which could similarly affect C1orf185 if it is regulated by this pathway. BAPTA/AM chelates intracellular calcium, potentially reducing the activity of calcium-dependent proteins and pathways that might influence C1orf185. Collectively, these inhibitors achieve a concerted diminution of C1orf185 activity by manipulating signaling pathways that govern the functional state of this protein.

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 phosphoinositide 3-kinase (PI3K) inhibitor. By inhibiting PI3K, it prevents the phosphorylation and activation of AKT, leading to reduced cellular proliferation and survival signals that might otherwise elevate C1orf185 activity.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Rapamycin is an mTOR inhibitor that impedes the mTORC1 signaling pathway, which is involved in protein synthesis and cell growth. Inhibition of mTORC1 may lead to a decrease in the cellular processes that require C1orf185 function.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

SB203580 is a specific inhibitor of p38 MAPK. By diminishing p38 MAPK activity, it could indirectly decrease the activity of proteins that are regulated by stress-activated pathways, potentially including C1orf185.

LY 294002

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

LY 294002 is another PI3K inhibitor that works similarly to Wortmannin. It diminishes AKT signaling, potentially reducing the functional activity of C1orf185 if it is downstream or affected by PI3K/AKT pathway.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

PD 98059 is a MEK inhibitor which may reduce ERK pathway signaling, possibly affecting proteins like C1orf185 that could be regulated by this pathway.

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 may alter transcription factor activity and decrease the activity of proteins regulated by JNK, such as C1orf185 if applicable.

NSC 23766

733767-34-5sc-204823
sc-204823A
10 mg
50 mg
$151.00
$609.00
75
(4)

NSC 23766 inhibits Rac1 activation, which might lead to a decrease in actin cytoskeleton remodeling. If C1orf185 function is associated with cellular structure or motility, this compound could indirectly decrease its activity.

PP 1

172889-26-8sc-203212
sc-203212A
1 mg
5 mg
$86.00
$145.00
6
(1)

PP2 is an Src family tyrosine kinase inhibitor. By inhibiting Src kinases, it may diminish downstream signaling that could regulate C1orf185 activity.

BAPTA/AM

126150-97-8sc-202488
sc-202488A
25 mg
100 mg
$138.00
$458.00
61
(2)

BAPTA/AM is a cell-permeable calcium chelator, which by lowering intracellular calcium levels, could reduce the activity of calcium-dependent proteins and signaling pathways potentially influencing C1orf185 activity.

Y-27632, free base

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

Y-27632 is a ROCK inhibitor, decreasing the activity of Rho-associated protein kinases involved in cytoskeletal dynamics. If C1orf185 is involved in processes regulated by ROCK, this inhibitor could diminish its activity.