Inhibitors of LOC100041458 can be Wortmannin and Triciribine target the PI3K/AKT pathway, a crucial signaling route for regulating cell survival and metabolism. Inhibition of this pathway by either chemical impedes the cascade of events that could be necessary for the proper functioning or regulation of LOC100041458, particularly if it is involved in cell survival mechanisms. Similarly, U0126 and PD0325901, both MEK inhibitors, and SB203580, a p38 MAP kinase inhibitor, act on the MAPK pathway which is another critical signaling mechanism for cell proliferation, differentiation, and stress responses. By inhibiting these kinases, these chemicals can alter the activity of LOC100041458, especially if it is a part of this signaling network. Ibrutinib and Gefitinib, which target BTK and EGFR tyrosine kinases respectively, affect receptor signaling pathways that are integral to cell growth and proliferation. If LOC100041458 functions within these pathways, its activity would be influenced by these inhibitors.
The chemical class also includes ZM-447439 and Palbociclib, which inhibit Aurora kinases and CDK4/6 respectively, playing essential roles in cell cycle regulation. Their inhibitory effects on these kinases can alter the cell cycle events in which LOC100041458 may have a role. S3I-201, which disrupts STAT3 signaling, can impact various transcriptional responses, and if LOC100041458 is implicated in such genomic responses, its activity would be affected by this inhibitor. Finally, the class comprises Bortezomib and MG-132, both of which are proteasome inhibitors.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Inhibits PI3K, affecting the PI3K/AKT signaling pathway which can regulate cell survival and is often associated with protein activity modulation. | ||||||
Triciribine | 35943-35-2 | sc-200661 sc-200661A | 1 mg 5 mg | $102.00 $138.00 | 14 | |
Specifically inhibits AKT, altering downstream signaling that may govern processes LOC100041458 is involved in. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
Inhibits p38 MAP kinase, which can modulate stress response and inflammatory pathways that LOC100041458 may participate in. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $153.00 | 5 | |
Inhibits Bruton's tyrosine kinase (BTK), potentially disrupting B cell receptor signaling pathways involving LOC100041458. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
Selectively inhibits Aurora kinase activity, which can affect cell cycle progression that LOC100041458 may be connected to. | ||||||
Stat3 Inhibitor VI, S3I-201 | 501919-59-1 | sc-204304 | 10 mg | $148.00 | 104 | |
Inhibits STAT3 dimerization and DNA binding, potentially influencing transcription processes LOC100041458 is associated with. | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $62.00 $112.00 $214.00 $342.00 | 74 | |
Inhibits EGFR tyrosine kinase, which can affect growth factor signaling pathways involving LOC100041458. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
Inhibits CDK4/6, which can regulate cell cycle progression potentially involving LOC100041458. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Proteasome inhibitor, affecting protein degradation pathways that LOC100041458 may be part of or regulated by. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
Also a proteasome inhibitor, can affect ubiquitin-proteasome pathways, potentially regulating LOC100041458 stability or turnover. | ||||||