hCG_1988300 Inhibitors
HCG_1988300 Inhibitors belong to a distinct chemical class designed to selectively impede the activity of the specific biomolecule identified by the designation hCG_1988300. This chemical class represents a targeted approach within the realms of molecular biology and pharmacology, aiming to elucidate the intricate roles played by hCG_1988300 within cellular pathways. The development of inhibitors for hCG_1988300 involves a comprehensive analysis of the structural and functional characteristics of this biomolecule, enabling researchers to discern its molecular interactions and potential contributions to cellular processes.
Researchers engaged in the study of hCG_1988300 Inhibitors meticulously design compounds that can interfere with the activity or binding sites of hCG_1988300. The primary objective is to modulate the functions of this biomolecule, providing researchers with essential tools to investigate its specific roles and downstream effects within cellular systems. By disrupting the normal interactions of hCG_1988300, these inhibitors contribute to a deeper understanding of the underlying molecular mechanisms. The research surrounding hCG_1988300 Inhibitors not only unveils the functional aspects of the targeted biomolecule but also advances our broader comprehension of cellular processes, offering crucial insights into the complexities of molecular interactions and their implications in diverse biological contexts.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cyclopamine | 4449-51-8 | sc-200929 sc-200929A | 1 mg 5 mg | $92.00 $204.00 | 19 | |
Cyclopamine is a steroidal alkaloid that inhibits the Hedgehog signaling pathway, which is involved in the regulation of gene expression. Inhibition of this pathway can result in the downregulation of target genes. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a specific inhibitor of PI3K (phosphoinositide 3-kinase). PI3K is part of a cellular signaling pathway that can regulate gene expression, so inhibiting PI3K can lead to changes in the expression of genes downstream in the signaling pathway. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is an inhibitor of MEK, which is a kinase involved in the MAPK/ERK pathway, a key signaling pathway that regulates gene expression. Inhibiting this pathway can result in altered expression of certain genes. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of JNK (c-Jun N-terminal kinase), which is part of a signaling pathway that can affect transcription factors and gene expression. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a specific inhibitor of p38 MAP kinase, which is involved in cellular stress responses and can also affect gene expression. | ||||||
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 potent inhibitor of PI3K, affecting the AKT signaling pathway, which plays a role in regulating gene expression. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin is an mTOR inhibitor that affects a key cellular growth and proliferation pathway, which can result in changes in gene expression profiles. | ||||||
17-AAG | 75747-14-7 | sc-200641 sc-200641A | 1 mg 5 mg | $66.00 $153.00 | 16 | |
17-AAG is an inhibitor of Hsp90, a chaperone protein that stabilizes many client proteins, including several signaling molecules that regulate gene expression. | ||||||
Kenpaullone | 142273-20-9 | sc-200643 sc-200643A sc-200643B sc-200643C | 1 mg 5 mg 10 mg 25 mg | $60.00 $150.00 $226.00 $495.00 | 1 | |
Kenpaullone is an inhibitor of cyclin-dependent kinase (CDK), which can affect cell cycle progression and gene expression. | ||||||
2-Methoxyestradiol | 362-07-2 | sc-201371 sc-201371A | 10 mg 50 mg | $70.00 $282.00 | 6 | |
2-Methoxyestradiol is a natural metabolite of estradiol that can inhibit HIF-1α and angiogenesis, affecting cellular responses to hypoxia and potentially impacting gene expression related to hypoxic adaptation. | ||||||