STH1 inhibitors belong to a class of chemical compounds designed to target and modulate the activity of the STH1 protein. STH1, short for "Specificity factor TFIID subunit 1," is a critical component of the transcription initiation complex in eukaryotic cells, which plays a central role in gene expression regulation. The process of gene transcription begins with the binding of transcription factors, including TFIID, to the promoter region of a gene. STH1, as part of the TFIID complex, facilitates the recognition and binding of the RNA polymerase enzyme to the promoter, initiating transcription. However, in certain pathological conditions or research contexts, it may be necessary to regulate or inhibit STH1 activity, which is where STH1 inhibitors come into play.
STH1 inhibitors are typically designed to disrupt the normal functioning of the STH1 protein. This disruption can occur through various mechanisms, including competitive binding to the active site of STH1, interference with protein-protein interactions within the transcription initiation complex, or destabilization of the TFIID complex itself. By inhibiting STH1, researchers can gain insights into the molecular mechanisms of gene expression and develop tools for studying specific gene functions or regulatory pathways. Moreover, STH1 inhibitors have the potential to serve as valuable research reagents for investigating the roles of STH1 in various cellular processes, including development, differentiation, and disease progression. Researchers continue to explore the design and application of STH1 inhibitors as a means to expand our understanding of gene regulation and its implications in biology and beyond.
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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 | |
Broad-spectrum protein kinase inhibitor by ATP competition. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
Selective p38 MAP kinase inhibitor. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
PI3K inhibitor that blocks Akt activation. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Irreversible PI3K inhibitor via covalent modification. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
mTOR inhibitor, disrupting cell cycle and growth signals. | ||||||
Tozasertib | 639089-54-6 | sc-358750 sc-358750A | 25 mg 50 mg | $62.00 $87.00 | 4 | |
Aurora kinase inhibitor, interfering with cell division. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
BCR-ABL tyrosine kinase inhibitor in CML therapy. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Multi-kinase inhibitor with anti-angiogenic effects. | ||||||
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 | $87.00 $135.00 $293.00 $505.00 $3827.00 | 42 | |
EGFR tyrosine kinase inhibitor for cancer | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
Dual BCR-ABL and Src family kinase inhibitor. | ||||||