TFE3 inhibitors represent a diverse class of chemical entities meticulously crafted to modulate the activity of the transcription factor E3 (TFE3). TFE3 is a vital member of the microphthalmia-associated transcription factor (MiTF) family, recognized for its pivotal role in the intricate orchestration of gene expression. These inhibitors are ingeniously designed to exert influence over the functions of TFE3, which are indispensable for fundamental cellular processes such as growth, differentiation, and proliferation. Notably, the overarching objective of TFE3 inhibitors revolves around their capability to disrupt the typical functioning of this transcription factor.
In terms of chemical composition, TFE3 inhibitors encompass a broad spectrum of molecular structures. Some of these compounds are constituted by small organic molecules, whereas others are synthetically engineered compounds meticulously tailored to interact with distinct regions of TFE3 or its associated proteins. The mechanisms through which these inhibitors operate are remarkably diverse, ranging from interference with the nuclear-cytoplasmic translocation of TFE3 to impeding its activation through post-translational modifications like neddylation. Additionally, TFE3 inhibitors may target downstream signaling pathways, such as the mTOR pathway, which significantly influences TFE3 activity. The development and refinement of TFE3 inhibitors necessitate a profound comprehension of the intricate molecular interactions involved in TFE3 regulation, coupled with an in-depth understanding of the specific contexts in which TFE3 dysregulation occurs. Consequently, researchers in this field continually push the boundaries of chemical design to enhance the specificity and efficacy of TFE3 inhibitors, offering promising prospects for the precise modulation of this transcription factor's activity in diverse biological contexts.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | $280.00 | 1 | |
MLN4924 inhibits the NEDD8-activating enzyme (NAE) and indirectly suppresses TFE3 by preventing its activation through neddylation. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG-132 is a proteasome inhibitor that can lead to the accumulation of TFE3 and its degradation. | ||||||
KPT 330 | 1393477-72-9 | sc-489062 | 5 mg | $170.00 | ||
KPT-330 is an XPO1 (Exportin 1/CRM1) inhibitor that can disrupt the nuclear-cytoplasmic shuttling of TFE3. | ||||||
INK 128 | 1224844-38-5 | sc-364511 sc-364511A | 5 mg 50 mg | $315.00 $1799.00 | ||
INK 128 is an mTORC1/2 inhibitor that can indirectly inhibit TFE3 through the mTOR pathway. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $128.00 $638.00 | 7 | |
Everolimus is another mTOR inhibitor that can suppress TFE3 activity by inhibiting mTORC1. | ||||||
OSU 03012 | 742112-33-0 | sc-364560 sc-364560A | 5 mg 25 mg | $107.00 $342.00 | 1 | |
OSU 03012 is a small molecule that has been shown to inhibit TFE3 expression and activity in research studies. | ||||||
AZD2014 | 1009298-59-2 | sc-364420 | 5 mg | $303.00 | 2 | |
AZD2014 is an mTOR inhibitor that can target both mTORC1 and mTORC2, potentially affecting TFE3 activity in cancer cells. | ||||||