Chemical inhibitors of OSTF1 offer various approaches to impede its activity by targeting signaling pathways and enzymes that are crucial for its functional state. Staurosporine and Bisindolylmaleimide I act by inhibiting protein kinases that are central to phosphorylation, a post-translational modification essential for OSTF1 activation. Staurosporine is a broad-spectrum protein kinase inhibitor, which can prevent the phosphorylation of OSTF1, thus maintaining it in an inactive state. Bisindolylmaleimide I, as a selective inhibitor of Protein Kinase C (PKC), could reduce OSTF1 activity by hindering PKC-mediated signaling pathways that might be necessary for OSTF1's optimal function. Similarly, LY294002 and Wortmannin, both PI3K inhibitors, can lead to a reduction in Akt activity, an essential component of OSTF1 signaling, thereby attenuating OSTF1's activity. This is due to their ability to block the PI3K/Akt pathway, which is often upstream of various proteins, including OSTF1.
In a related vein, U0126 and PD98059, which are inhibitors of MEK1/2, and SB203580, a p38 MAPK inhibitor, can decrease OSTF1 activity by obstructing the MAPK pathway. U0126 and PD98059 prevent the activation of ERK, thus potentially leading to a reduction in OSTF1 activity that is regulated via ERK signaling. SB203580 acts on the p38 MAPK, and its inhibition would result in decreased OSTF1 phosphorylation and subsequent activity. The JNK inhibitor SP600125 can also diminish OSTF1 activity by interfering with the JNK signaling that may be essential for the activation of OSTF1. Rapamycin, an mTOR inhibitor, can indirectly diminish OSTF1 activity by acting on mTOR, a key regulator of cell growth that may interact with OSTF1-regulated pathways. PP2, a Src family kinase inhibitor, and Y-27632, a ROCK inhibitor, can attenuate OSTF1 activity by impeding the activation signaling from Src family kinases and Rho/ROCK signaling, respectively, which could be necessary for OSTF1's function. Lastly, Gefitinib, by inhibiting the EGFR tyrosine kinase, can lead to a decrease in OSTF1 activity, as it would impede the downstream signaling events that activate OSTF1.
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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 $150.00 $388.00 | 113 | |
Staurosporine is a potent inhibitor of protein kinases. OSTF1, being a signal transduction protein, relies on phosphorylation for its activity. Inhibition of the kinases that phosphorylate OSTF1 would result in its functional inhibition as it would remain in an unphosphorylated, and thus inactive, state. | ||||||
Bisindolylmaleimide I (GF 109203X) | 133052-90-1 | sc-24003A sc-24003 | 1 mg 5 mg | $103.00 $237.00 | 36 | |
Bisindolylmaleimide I specifically inhibits Protein Kinase C (PKC). If OSTF1 activity is dependent on PKC-mediated signaling, the inhibition of PKC would lead to a reduction in OSTF1 activity due to a lack of activating phosphorylation. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is an inhibitor of PI3K, which is upstream in many signaling pathways. Inhibition of PI3K would lead to reduced Akt activity, which may be necessary for OSTF1 function, thereby resulting in a decrease in OSTF1 activity. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
U0126 is an inhibitor of MEK1/2, which are upstream of ERK in the MAPK pathway. OSTF1 activity that relies on ERK signaling would be inhibited due to the blockade of ERK activation by U0126. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is an inhibitor of p38 MAPK. If OSTF1 function is modulated by p38 MAPK signaling, the inhibition of this kinase would lead to a decrease in OSTF1 activity by preventing its required phosphorylation. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is a MEK inhibitor, which prevents the activation of ERK. Inhibition of this pathway would result in reduced OSTF1 activity if OSTF1 is functionally regulated via ERK signaling. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of JNK. If OSTF1 relies on JNK signaling for its activity, the inhibition of JNK would reduce OSTF1 activity by preventing activation-related phosphorylation events. | ||||||
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 PI3K inhibitor. By inhibiting PI3K, downstream signaling required for OSTF1 activity, such as Akt activation, would be inhibited, resulting in a decrease in OSTF1 functional activity. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin inhibits mTOR, which is a central protein in cell growth and metabolism regulation. Inhibition of mTOR could lead to a decrease in OSTF1 activity if OSTF1 is involved in mTOR-regulated pathways. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
PP2 is an Src family kinase inhibitor. If OSTF1's function is influenced by Src family kinase activity, inhibition by PP2 would reduce OSTF1 activity through reduced activation signaling. | ||||||