CKR-9 Inhibitors as a chemical class refers to a group of compounds that modulate the activity of the CKR-9 protein indirectly by targeting various signaling molecules and pathways that CKR-9 may be involved with. These compounds, although not directly interacting with CKR-9, can affect the protein's function by altering the signaling landscape within the cell. The compounds listed above are not specific to CKR-9 but have been chosen based on their ability to inhibit common signaling pathways that are often interconnected with regulatory proteins.
The inhibitors span several classes of kinase inhibitors, each with a specific target within cellular signaling pathways. Staurosporine, LY294002, and wortmannin are broad-spectrum kinase inhibitors that can disrupt a wide range of signaling processes, potentially affecting the activity of CKR-9 by altering upstream signals or downstream effects. U0126, SP600125, SB203580, and PD98059 target the MAPK signaling cascade, a pathway that regulates various cellular responses, including proliferation, differentiation, and stress responses. PP2 and GF109203X are more specific in their inhibition of Src family kinases and protein kinase C, respectively, which can alter the phosphorylation status of proteins and change cellular dynamics. Rapamycin targets the mTOR pathway, which is central to cell growth and metabolism.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
A potent inhibitor of protein kinases, can disrupt signal transduction pathways that CKR-9 may be part of. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor, can block the PI3K/Akt pathway that could be upstream or downstream of CKR-9. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits JNK, could disrupt JNK signaling pathways that may involve CKR-9. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
A selective inhibitor of p38 MAP kinase, can affect stress response pathways linked with CKR-9. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $94.00 $227.00 | 30 | |
Inhibits Src family kinases, possibly altering signaling cascades that include CKR-9. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Inhibits mTOR, which could be a part of the signaling network involving CKR-9. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
Inhibits MEK, which might affect pathways associated with CKR-9 activity. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
A PI3K inhibitor, can disrupt signaling pathways that CKR-9 is potentially involved in. | ||||||
Bisindolylmaleimide I (GF 109203X) | 133052-90-1 | sc-24003A sc-24003 | 1 mg 5 mg | $105.00 $242.00 | 36 | |
Inhibits protein kinase C, could impact signaling mechanisms in which CKR-9 participates. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $153.00 $356.00 | 15 | |
Inhibits Aurora kinase, and may interfere with cell division processes that CKR-9 could influence. | ||||||