Date published: 2026-6-6

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C20orf135 Inhibitors

The approach to inhibiting C20orf135 is primarily indirect due to the limited knowledge regarding the specific functions and pathways associated with this protein. Chemicals such as Staurosporine, LY294002, and Rapamycin target a wide range of pathways, from kinase activity and the PI3K pathway to the mTOR pathway. By modulating these pathways, they can influence the activity or expression of a myriad of downstream targets, which may include C20orf135. Agents like MG132 and Cycloheximide, which inhibit protein degradation and synthesis, respectively, provide a broad method to impact protein function and stability, influencing proteins of unknown or under-studied functions.

Similarly, inhibitors like Nocodazole and Calyculin A, which affect cell cycle progression and phosphorylation status, offer a broad strategy to influence the cellular environment. Such agents can modulate the activity, localization, or stability of a variety of proteins, even those with less-defined roles like C20orf135. With the current understanding, targeting C20orf135 specifically remains challenging. Therefore, a broader, pathway-centric approach provides an avenue to indirectly modulate its function.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$153.00
$396.00
113
(4)

General kinase inhibitor. By broadly inhibiting kinase activity, it might indirectly alter C20orf135 if it relies on phosphorylation events for its function or stability.

LY 294002

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

PI3K inhibitor. If C20orf135 operates within or downstream of the PI3K pathway, this inhibitor might indirectly modulate its activity or expression.

Rapamycin

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

mTOR inhibitor. If C20orf135 is involved in processes regulated by mTOR, such as protein synthesis or autophagy, Rapamycin can indirectly influence its function.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

Proteasome inhibitor. If C20orf135 undergoes proteasomal degradation, MG132 can enhance its stability and prolong its cellular presence.

Nocodazole

31430-18-9sc-3518B
sc-3518
sc-3518C
sc-3518A
5 mg
10 mg
25 mg
50 mg
$59.00
$85.00
$143.00
$247.00
38
(2)

Microtubule depolymerizing agent. If C20orf135 is involved in cell cycle events or relies on microtubule dynamics, Nocodazole might indirectly affect its function.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$41.00
$84.00
$275.00
127
(6)

Protein synthesis inhibitor. If C20orf135 has a short half-life or its synthesis is triggered by specific stimuli, Cycloheximide can indirectly prevent its accumulation.

Calyculin A

101932-71-2sc-24000
sc-24000A
10 µg
100 µg
$163.00
$800.00
59
(3)

PP1 and PP2A phosphatase inhibitor. If C20orf135's activity or function is regulated by dephosphorylation events, Calyculin A might impact it indirectly.

PD 98059

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

MEK inhibitor. If C20orf135 is in any way associated with the MAPK signaling cascade, PD98059 can affect its function or expression indirectly.

Wortmannin

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

PI3K inhibitor. Like LY294002, if C20orf135's function or expression relies on the PI3K-Akt pathway, Wortmannin can modulate it indirectly.

2-Deoxy-D-glucose

154-17-6sc-202010
sc-202010A
1 g
5 g
$70.00
$215.00
26
(2)

Glucose analog inhibiting glycolysis. If C20orf135 has roles in metabolism or cellular energy processes, its function might be indirectly altered by this compound.