Chemical inhibitors of ZNF30 can affect the protein's function by disrupting various cellular signaling pathways that regulate its activity. Wortmannin and LY294002 are inhibitors targeting the phosphoinositide 3-kinases (PI3K) pathway, which plays a crucial role in many cellular processes, including the activation of DNA binding and transcription factors. By inhibiting PI3K, these chemicals can reduce the phosphorylation and activation of proteins downstream in the PI3K pathway, which may be necessary for ZNF30's regulatory functions. Similarly, Rapamycin, an mTOR inhibitor, disrupts the mTOR signaling pathway, which is also critical for regulating protein synthesis and other cellular processes that could involve ZNF30. The inhibition by Rapamycin can lead to a decrease in the function of proteins essential for ZNF30's activity.
Further inhibitors, such as Staurosporine and Dasatinib, target a wide range of protein kinases. Staurosporine is known for its broad-spectrum kinase inhibition, which can include kinases involved in the regulation of transcription factors like ZNF30. Dasatinib specifically inhibits Src family kinases and BCR-ABL kinases, which are integral to several signaling pathways that influence the activity of transcription factors. By blocking these kinases, both Staurosporine and Dasatinib can decrease the phosphorylation state of ZNF30, potentially inhibiting its functional conformation and DNA binding ability. Additionally, U0126 and PD98059 are inhibitors of the MEK1/2 kinases within the MAPK/ERK pathway. Inhibiting MEK1/2 leads to a reduction in ERK activation, which could decrease the phosphorylation and subsequent activity of ZNF30. SB203580 and SP600125 inhibit the p38 MAPK and JNK pathways, respectively, which could further decrease the functional activity of ZNF30 by preventing necessary phosphorylation events. Lastly, LFM-A13 and PP2, by inhibiting Bruton's tyrosine kinase and Src family kinases, respectively, can interfere with signaling pathways that may affect the functional activity of ZNF30, leading to its inhibition.
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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 | $67.00 $223.00 $425.00 | 97 | |
Wortmannin acts as an inhibitor of phosphoinositide 3-kinases (PI3K), which are involved in various signaling pathways, including those regulating DNA binding and transcription factors such as ZNF30. Inhibition of PI3K can lead to reduced phosphorylation and activation of downstream targets that may be necessary for ZNF30 to exert its function, thereby inhibiting ZNF30's activity. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
Staurosporine is a potent inhibitor of protein kinases. It is known to inhibit a broad spectrum of kinases, which could include those involved in the phosphorylation and regulation of ZNF30. By preventing the activation of these kinases, staurosporine can inhibit the phosphorylation state of ZNF30, which may be necessary for its functional conformation and binding to DNA or interaction with other proteins, thus functionally inhibiting ZNF30. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is a specific inhibitor of PI3K, which can affect the activity of downstream proteins involved in the signaling pathways that regulate functions of transcription factors like ZNF30. By inhibiting PI3K, LY294002 can impair the phosphorylation and activation of these proteins, potentially inhibiting the function of ZNF30 through decreased activation of signaling pathways required for its activity. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin is an mTOR inhibitor which can disrupt the mTOR signaling pathway. Since mTOR can regulate protein synthesis and other cellular processes that may involve ZNF30, inhibiting mTOR with rapamycin could lead to reduced function of proteins that are necessary for the activity of ZNF30, thereby functionally inhibiting ZNF30. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 is an inhibitor of MEK1/2, which are upstream of extracellular signal-regulated kinases (ERK). ERKs can phosphorylate various substrates, including transcription factors. Inhibition of MEK1/2 by U0126 can reduce ERK activation and consequently decrease the phosphorylation of transcription factors like ZNF30, which may rely on such phosphorylation for its activity, thus functionally inhibiting ZNF30. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB203580 is a well-known p38 MAPK inhibitor. By inhibiting p38 MAP kinase, SB203580 can suppress the phosphorylation of substrates involved in inflammatory responses and stress signaling, which could include transcription factors like ZNF30. The inhibition of p38 MAPK could therefore decrease the functional activity of ZNF30 by preventing necessary phosphorylation events that contribute to ZNF30's role in gene expression regulation. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of c-Jun N-terminal kinase (JNK), which can phosphorylate a variety of transcription factors. By inhibiting JNK, SP600125 can prevent the phosphorylation and subsequent activation of proteins that may interact with or regulate ZNF30, thus potentially inhibiting the functional activity of ZNF30. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD98059 acts as an inhibitor of MEK, which is involved in the MAPK/ERK pathway. By inhibiting MEK activity, PD98059 can decrease ERK phosphorylation and its associated downstream signaling, which may affect transcription factors like ZNF30. Reduced activation of this signaling pathway can inhibit the functional activity of ZNF30 by preventing the phosphorylation that is essential for its activity. | ||||||
LFM-A13 | 62004-35-7 | sc-203623 sc-203623A | 10 mg 50 mg | $119.00 $670.00 | ||
LFM-A13 is a selective inhibitor of Bruton's tyrosine kinase (Btk). Btk is involved in the regulation of various signaling pathways related to cell survival and proliferation. By inhibiting Btk, LFM-A13 can interfere with these signaling pathways, which may affect the functional activity of transcription factors like ZNF30 that could be regulated by these pathways, leading to functional inhibition of ZNF30. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $94.00 $227.00 | 30 | |
PP2 is an inhibitor of Src family kinases. Src kinases can influence multiple cellular processes, including those that regulate the activity of transcription factors. Inhibition of Src kinases by PP2 can result in decreased phosphorylation and activation of proteins that may interact with or control the function of ZNF30, leading to functional inhibition of ZNF30. | ||||||