Staurosporine, a potent kinase inhibitor, has broad applications in cellular signaling research due to its ability to block a wide array of kinases, potentially impacting various signaling cascades within the cell. By inhibiting these essential enzymes, Staurosporine could alter the activity of a myriad of proteins, including the protein LOC729531, should it be regulated by or interact with protein kinases. Similarly, Rapamycin, known for its specific inhibition of the mTOR pathway, could affect the activity of LOC729531 by modulating cell growth and metabolism if LOC729531 were involved in processes regulated by mTOR. Cyclosporine A, an immunosuppressant that inhibits calcineurin, might also indirectly impact LOC729531 by altering the NFAT pathway, which is crucial for T-cell activation and other immune responses. This could potentially affect proteins associated with or regulated by calcineurin signaling. Meanwhile, 5-Fluorouracil interferes with nucleotide synthesis, influencing DNA replication and repair processes, which could affect proteins like LOC729531 if it plays a role in these crucial cellular mechanisms.
The proteasome inhibitor Bortezomib could affect the stability and turnover of LOC729531 by inhibiting the degradation machinery within the cell, potentially leading to an accumulation of proteins that are normally marked for destruction. Trichostatin A, as an HDAC inhibitor, might change the expression levels of LOC729531 by altering chromatin structure and gene transcription patterns. Inhibitors like LY294002 and Wortmannin target the PI3K/Akt pathway, affecting cell survival and metabolism, which might alter the function of proteins involved in this pathway, including LOC729531. MEK inhibitors such as PD98059 and U0126 could impact the MAPK/ERK pathway, influencing cell division and differentiation processes that LOC729531 might be part of. Finally, SB203580, targeting p38 MAP kinase, could modify inflammatory responses and apoptosis, potentially affecting LOC729531 if it is involved in these processes. MG132, another proteasome inhibitor, could similarly influence protein turnover and function, including that of LOC729531.
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| 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 | |
Wortmannin is a steroidal metabolite of the fungi Penicillium funiculosum that acts as a potent and irreversible inhibitor of phosphoinositide 3-kinases (PI3K), which can affect various cellular processes, including those related to protein signaling. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a synthetic molecule that inhibits PI3K, potentially impacting signaling cascades that regulate protein function and expression. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a synthetic compound that inhibits p38 MAP kinase, which is involved in inflammatory responses and cell differentiation. It may influence proteins that are regulated by or interact with the p38 MAP kinase pathway. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is a synthetic compound that inhibits MEK, which is part of the MAPK/ERK pathway. This pathway is implicated in cell growth and development, and its inhibition may affect proteins regulated by this pathway. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an anthrapyrazolone inhibitor of c-Jun N-terminal kinase (JNK), modulating processes such as apoptosis and cellular differentiation that could have downstream effects on a variety of proteins. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
U0126 is a synthetic compound that selectively inhibits MEK1 and MEK2, components of the MAPK/ERK pathway, potentially altering the function or stability of proteins involved in this pathway. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin is a macrolide compound that inhibits mTOR, a key regulator of cell growth and metabolism, which might affect proteins that are regulated by or interact with the mTOR pathway. | ||||||
Cyclosporin A | 59865-13-3 | sc-3503 sc-3503-CW sc-3503A sc-3503B sc-3503C sc-3503D | 100 mg 100 mg 500 mg 10 g 25 g 100 g | $62.00 $90.00 $299.00 $475.00 $1015.00 $2099.00 | 69 | |
Cyclosporin A is a cyclic peptide that inhibits calcineurin, thereby inhibiting T-cell activation. Its action can influence signaling pathways and proteins involved in immune responses. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib is a boronic acid derivative that inhibits the 26S proteasome, potentially affecting protein degradation pathways and altering levels of various proteins within the cell. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $94.00 $349.00 | 114 | |
Thapsigargin is a sesquiterpene lactone that inhibits the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), affecting calcium homeostasis in cells and potentially influencing proteins sensitive to calcium levels. | ||||||