Zic1 inhibitors belong to a specific class of chemical compounds designed to target and modulate the activity of the zinc finger transcription factor Zic1. The Zic family of proteins plays a crucial role in the regulation of embryonic development, cell differentiation, and tissue patterning. Zic1, in particular, has been identified as a key player in various cellular processes, including neurogenesis and axial patterning during early embryonic development. By selectively inhibiting the function of Zic1, these inhibitors aim to elucidate the intricate regulatory mechanisms underlying these biological processes.
The molecular structure of Zic1 inhibitors is characterized by their ability to bind specifically to the active site of the Zic1 protein, thereby interfering with its transcriptional activity. Typically, these inhibitors are small molecules with well-defined chemical structures, allowing for precise interactions with the target protein. The development of Zic1 inhibitors involves a thorough understanding of the three-dimensional structure of the Zic1 protein, enabling medicinal chemists to design compounds that can effectively disrupt its function. This class of compounds holds promise as valuable research tools for investigating the fundamental molecular mechanisms.
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