Date published: 2025-12-18

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HOM-TES-103 Inhibitors

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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Items 11 to 12 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

17-AAG

75747-14-7sc-200641
sc-200641A
1 mg
5 mg
$66.00
$153.00
16
(2)

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

331771-20-1sc-200696
sc-200696A
1 mg
10 mg
$150.00
$349.00
15
(1)

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.