HOM-TES-103 inhibitors encompass a range of compounds that, through their distinct mechanisms of action, can lead to the reduced activity of HOM-TES-103. These compounds do not directly target HOM-TES-103 but intervene in the signaling pathways and cellular processes that regulate its function. For example, inhibitors like staurosporine and dasatinib interfere with kinase signaling that HOM-TES-103 may depend upon. If HOM-TES-103's activity is contingent on phosphorylation events catalyzed by specific kinases, then staurosporine's broad kinase inhibition profile could lead to an indirect decrease in HOM-TES-103 activity by preventing necessary phosphorylation events. Similarly, dasatinib's inhibition of BCR-ABL and Src family kinases would lead to decreased activity of HOM-TES-103 if tyrosine kinase signaling from these kinases is required for its activity.
Likewise, compounds such as LY294002 and wortmannin target the PI3K/Akt pathway. If the activity of HOM-TES-103 is PI3K/Akt-dependent, inhibition by these compounds would lead to a decrease in HOM-TES-103 activity by reducing the downstream signaling cascade necessary for HOM-TES-103 activation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
17-AAG | 75747-14-7 | sc-200641 sc-200641A | 1 mg 5 mg | $66.00 $153.00 | 16 | |
17-AAG is an Hsp90 inhibitor which leads to the degradation of client proteins. If HOM-TES-103 is an Hsp90 client protein, its stability and function could be compromised by 17-AAG. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
ZM-447439 is an Aurora kinase inhibitor. If HOM-TES-103 is involved in cell cycle regulation where Aurora kinases play a role, inhibition by ZM-447439 could result in reduced activity of HOM-TES-103. | ||||||