FLJ23861 inhibitors are a class of small molecules designed to target and modulate the activity of the protein encoded by the FLJ23861 gene, which is associated with various cellular processes. The FLJ23861 protein, although not extensively characterized, is believed to play a role in regulating cellular signaling pathways, protein interactions, and possibly gene expression. Inhibitors of FLJ23861 act by binding to the protein, preventing its normal function, which may result in the alteration of downstream signaling events. This inhibition can lead to changes in cellular functions such as proliferation, differentiation, and survival, depending on the specific pathways and processes influenced by the FLJ23861 protein.
The structural properties of FLJ23861 inhibitors typically include small, lipophilic compounds that are capable of crossing cellular membranes, allowing them to act intracellularly. These inhibitors are designed to be highly specific to the FLJ23861 protein, minimizing off-target effects on other proteins within the cell. The molecular design of these inhibitors often involves optimizing the binding affinity to the FLJ23861 protein's active or allosteric sites, ensuring effective modulation of its activity. The chemical structures of FLJ23861 inhibitors can vary, but they frequently include functional groups that facilitate strong binding interactions such as hydrogen bonding, hydrophobic interactions, or van der Waals forces, making them potent modulators of the protein's activity. This specificity and potency are crucial for studying the biological role of FLJ23861 in various in vitro and in vivo experimental systems.
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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 | |
PI3K inhibitor that affects AKT signaling, which is a common pathway in cellular growth and survival. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
Another PI3K inhibitor, similar to Wortmannin, that can disrupt downstream signaling pathways. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
Inhibits MEK1, which could affect the MAPK/ERK pathway, a central signaling pathway that regulates cell division. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
P38 MAPK inhibitor that impacts stress response signaling and inflammation-related pathways. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits JNK, which can influence apoptotic and survival signaling pathways within the cell. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
A selective inhibitor of MEK1/2, known to block the MAPK/ERK signaling pathway. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
mTOR inhibitor affecting cell growth, proliferation, and survival pathways. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Proteasome inhibitor, influencing NF-kB signaling and the degradation of cell-cycle regulatory proteins. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
Src family kinase inhibitor, which can alter multiple cellular signaling pathways, including cell migration and proliferation. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
BCR-ABL and Src family kinase inhibitor, impacting signal transduction pathways related to cell growth and division. | ||||||