Date published: 2025-10-12

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D630037F22Rik Inhibitors

The TBC1D32 Inhibitors represent a pharmacologically diverse array of compounds designed to modulate the function of TBC1D32, a protein intricately involved in various cellular processes, including animal organ development, non-motile cilium assembly, and the smoothened signaling pathway crucial for dorsal/ventral neural tube patterning. TBC1D32, orthologous to human TBC1D32, is predicted to be located in the cilium and cytoplasm and plays a vital role in cellular functions related to development and signaling cascades. Brefeldin A, a fungal metabolite, directly inhibits TBC1D32 by disrupting vesicular transport processes and the functioning of the Golgi apparatus. This disruption leads to impaired smoothened signaling and cilium assembly involved in dorsal/ventral neural tube patterning. Leptomycin B, an antifungal antibiotic, indirectly inhibits TBC1D32 by blocking nuclear export through CRM1, influencing cytoplasmic localization, and consequently disrupting processes such as animal organ development, non-motile cilium assembly, and smoothened signaling.

Wortmannin, a fungal metabolite, directly inhibits TBC1D32 by targeting PI3-kinase, affecting intracellular signaling pathways and disrupting smoothened signaling and cilium assembly essential for dorsal/ventral neural tube patterning and animal organ development. Dynasore, a dynamin inhibitor, indirectly inhibits TBC1D32 by blocking endocytosis, influencing cytoplasmic processes, and disrupting non-motile cilium assembly and smoothened signaling involved in dorsal/ventral neural tube patterning and animal organ development. AG-490, a JAK2 inhibitor, indirectly inhibits TBC1D32 by affecting the JAK-STAT pathway, disrupting signaling cascades, and consequently impairing smoothened signaling and non-motile cilium assembly involved in dorsal/ventral neural tube patterning and animal organ development. Collectively, these inhibitors offer a comprehensive toolkit for researchers investigating the multifaceted roles of TBC1D32 in cellular development and signaling processes. Understanding how these chemicals modulate TBC1D32 function sheds light on strategies for conditions associated with aberrant cellular processes governed by this protein.

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