C1orf161 inhibitors are a diverse array of chemical entities specially designed to attenuate the functionality of the C1orf161 protein by intervening in specific signaling pathways and cellular processes that are essential for its activity. These inhibitors are strategically targeted to disrupt key points within these pathways that are critical for C1orf161's role in the cell. For example, the functional connection between mTOR signaling and C1orf161 is exploited by compounds like Rapamycin, leading to a reduction in C1orf161's activity due to the crucial role of mTOR in protein synthesis and activity regulation. Inhibitors such as LY 294002 work by impeding PI3K/AKT signaling, a pathway integral to C1orf161's function, thus resulting in diminished activity of the protein.
Furthermore, the repertoire of C1orf161 inhibitors includes molecules that indirectly affect the protein's activity by targeting upstream or related signaling mechanisms. MEK inhibitors like PD 98059, U0126, and Trametinib reduce the activity of the ERK pathway, which C1orf161 depends on for its functional integrity, leading to an indirect but potent inhibition of the protein. Similarly, inhibitors such as Y-27632 and SB 203580 impact C1orf161 by altering cytoskeletal dynamics and cytokine signaling, respectively, processes that are closely tied to the protein's operational framework. These inhibitors, by acting on various regulatory molecules and pathways, collectively contribute to the attenuation of C1orf161 activity. They depict C1orf161 as a protein that is intricately woven into the cellular fabric, with its activity being modifiable through targeted chemical intervention at multiple regulatory points.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
A specific mTOR inhibitor. C1orf161's function is reduced as mTOR signaling is crucial for its protein synthesis and activity regulation. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
An MEK inhibitor that impedes the ERK pathway. C1orf161's activity is diminished due to its reliance on ERK signaling for functional support. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A PI3K inhibitor that disrupts AKT signaling. This leads to decreased C1orf161 activity as PI3K/AKT is involved in its functional pathway. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
A p38 MAPK inhibitor that disrupts cytokine signaling, thereby reducing C1orf161 activity as it is dependent on this pathway. | ||||||
WZ 4002 | 1213269-23-8 | sc-364655 sc-364655A | 10 mg 50 mg | $180.00 $744.00 | 1 | |
An EGFR inhibitor that reduces C1orf161 activity by inhibiting downstream signaling processes that C1orf161 is involved in. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
A ROCK inhibitor that diminishes cytoskeletal rearrangements, thereby inhibiting C1orf161 activity which is associated with these processes. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $65.00 $267.00 | 257 | |
A JNK inhibitor that diminishes C1orf161 activity by interrupting stress response signaling pathways C1orf161 is involved in. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
A receptor tyrosine kinase inhibitor that leads to reduced C1orf161 activity by inhibiting angiogenic signaling pathways. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $153.00 | 5 | |
A Bruton's tyrosine kinase inhibitor, decreasing C1orf161 activity by interrupting B-cell receptor signaling pathways. | ||||||
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
A MEK inhibitor that reduces C1orf161 activity through inhibition of the MEK/ERK pathway, which is crucial for its function. |