Date published: 2025-9-11

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brachyury 2 Activators

Brachyury 2, a key player in mesodermal differentiation, exhibits protein homodimerization activity and is involved in learning or memory, negative regulation of neuron apoptosis, and positive regulation of nervous system development. Predicted to be located in the cytosol and nucleoplasm, it is expressed in structures such as the central nervous system, sensory organs, skeleton, submandibular gland primordium, and trigeminal nerve. The human orthologs include ARMCX5-GPRASP2. To explore potential activators, we considered various chemicals that impact related pathways. Trichostatin A indirectly activates brachyury 2 by inhibiting HDAC, altering chromatin structure and gene expression. SB431542 indirectly activates brachyury 2 by inhibiting the TGF-β receptor, modulating TGF-β signaling and influencing processes related to mesoderm formation. CHIR99021 indirectly activates brachyury 2 by inhibiting GSK-3, impacting GSK-3-dependent pathways and processes related to mesoderm formation. Vorinostat indirectly activates brachyury 2 through HDAC inhibition, altering chromatin dynamics and transcriptional regulation.

A83-01 indirectly activates brachyury 2 by inhibiting the TGF-β receptor, modulating TGF-β signaling and influencing processes related to mesoderm formation. LDN-193189 indirectly activates brachyury 2 by inhibiting the BMP receptor, modulating BMP signaling and influencing processes related to mesoderm formation. 5-Azacytidine indirectly activates brachyury 2 by inhibiting DNA methyltransferase, altering DNA methylation patterns and gene expression. LDN-214117 indirectly activates brachyury 2 by inhibiting ALK2, modulating BMP signaling and influencing processes related to mesoderm formation. EPZ005687 indirectly activates brachyury 2 by inhibiting EZH2, altering chromatin structure and gene expression. Sodium butyrate indirectly activates brachyury 2 through HDAC inhibition, altering chromatin dynamics and transcriptional regulation. Y-27632 indirectly activates brachyury 2 by inhibiting ROCK, modulating cytoskeletal dynamics and influencing processes related to mesoderm formation. JQ1 indirectly activates brachyury 2 by inhibiting BET bromodomains, altering chromatin dynamics and transcriptional regulation. In summary, these chemicals indirectly influence brachyury 2 through various pathways, modulating chromatin structure, gene expression, cellular processes, and signaling cascades. The activation of brachyury 2 is intricately linked to these processes, contributing to its roles in mesodermal differentiation and the regulation of neural functions. The nuanced interplay between these activators and brachyury 2 highlights the complexity of the molecular mechanisms involved in the control of cell fate determination and developmental processes.

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