The term ASCL4 inhibitors refers to a class of chemical compounds designed to specifically target and modulate the activity of the ASCL4 protein or its associated signaling pathways within the context of cellular and molecular biology research. ASCL4, short for Achaete-scute family bHLH transcription factor 4, is a member of the basic helix-loop-helix (bHLH) transcription factor family. These transcription factors play a pivotal role in regulating gene expression and influencing various cellular processes, including cell differentiation and development. ASCL4 itself is recognized for its involvement in the determination of cell fate and the regulation of neural differentiation.
ASCL4 inhibitors typically comprise small molecules or compounds engineered to interfere with the function of ASCL4. The mechanism of action of these inhibitors often involves binding to ASCL4 or its upstream regulators, effectively disrupting its transcriptional activity. This interference can lead to the inhibition of downstream target genes that ASCL4 controls, thereby providing researchers with a tool to investigate the specific roles of ASCL4 in cellular processes. By modulating ASCL4 activity, scientists can gain insights into its function and the broader implications it has in various cellular contexts, shedding light on its role in development, tissue homeostasis, and potential contributions to diseases when dysregulated. In essence, ASCL4 inhibitors serve as valuable research tools, aiding in the dissection of intricate biological processes and paving the way for a deeper understanding of transcriptional regulation and its impacts on cell biology.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Acalabrutinib | 1420477-60-6 | sc-507392 | 250 mg | $255.00 | ||
Acalabrutinib is a selective Bruton's tyrosine kinase (BTK) inhibitor, which binds to BTK and inhibits its activity, disrupting B-cell receptor signaling in B-cell malignancies. | ||||||
ABT-199 | 1257044-40-8 | sc-472284 sc-472284A sc-472284B sc-472284C sc-472284D | 1 mg 5 mg 10 mg 100 mg 3 g | $116.00 $330.00 $510.00 $816.00 $1632.00 | 10 | |
Venetoclax is a B-cell lymphoma-2 (BCL-2) inhibitor that binds to BCL-2 proteins, blocking their interaction with pro-apoptotic proteins and promoting apoptosis in cancer cells. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $153.00 | 5 | |
Ibrutinib covalently binds to and inhibits BTK, a critical kinase in B-cell signaling pathways, leading to the suppression of B-cell proliferation and survival in B-cell malignancies. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
Palbociclib is a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor, disrupting cell cycle progression by inhibiting CDK4/6-mediated phosphorylation of retinoblastoma protein. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib inhibits the tyrosine kinases ABL1 and KIT, disrupting their signaling pathways. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib is a multi-kinase inhibitor that targets ABL1, SRC, and other kinases, inhibiting oncogenic signaling pathways involved in leukemia and solid tumors. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib inhibits multiple kinases, including RAF and VEGFR, disrupting MAPK and angiogenesis pathways in cancer cells and slowing tumor growth. | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $85.00 $132.00 $287.00 $495.00 $3752.00 | 42 | |
Erlotinib is an epidermal growth factor receptor (EGFR) inhibitor that competes with ATP for binding to EGFR, blocking downstream signaling and inhibiting cancer cell proliferation. | ||||||
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
Trametinib is a MEK inhibitor that targets the MAPK pathway, inhibiting the growth and proliferation of cancer cells in various malignancies. |