Date published: 2025-9-16

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Smurf2 Inhibitors

The class of Smurf2 inhibitors encompasses a diverse array of chemical compounds, each strategically designed to modulate Smurf2 activity either directly or indirectly through intricate cellular pathways. Caffeic acid, a polyphenolic compound found in various plants, has emerged as a potent indirect inhibitor of Smurf2 by exerting its influence on the transforming growth factor-beta (TGF-β) signaling pathway. In contrast, compounds such as LY364947 and A83-01 take a more direct route in inhibiting Smurf2 by specifically targeting the TGF-β receptor. LY364947, a pyrazole derivative, functions by disrupting Smurf2 recruitment and subsequent ubiquitination of TGF-β receptors. This selective interference curtails Smurf2's regulatory role in the TGF-β signaling pathway, offering a targeted approach to attenuate Smurf2-mediated cellular events. A83-01, another TGF-β receptor inhibitor, operates on a similar principle, further underscoring the significance of TGF-β receptor modulation as a viable strategy for Smurf2 inhibition.

TAK-243, a direct inhibitor of NEDD8-activating enzyme (NAE), represents a distinct class of Smurf2 inhibitors that act by disrupting cullin-RING ligase (CRL) function. As Smurf2 is a substrate of CRL, TAK-243-induced inhibition of neddylation prevents Smurf2 ubiquitination, stabilizing the protein and limiting its availability for substrate ubiquitination. The Smurf2 inhibitor class further expands with compounds like NSC 23766 and Amlexanox, which indirectly attenuate Smurf2 activity by influencing the RhoA and TAK1/MAPK pathways, respectively. NSC 23766, a selective inhibitor of RhoA-specific guanine nucleotide exchange factor (GEF), disrupts RhoA activation, impacting Smurf2 stability and subcellular localization. Amlexanox, on the other hand, targets the TAK1/MAPK pathway, inhibiting TAK1 activation and subsequently modulating Smurf2 expression and stability. Closing the spectrum of Smurf2 inhibitors is MLN4924, a direct inhibitor of NEDD8-activating enzyme (NAE). Operating on a similar principle as TAK-243, MLN4924 disrupts CRL function by preventing neddylation, thereby stabilizing Smurf2 and limiting its availability for substrate ubiquitination.

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