Fibrinogen γ inhibitors are a class of chemical compounds specifically designed to target and interact with fibrinogen γ, a crucial protein involved in the blood clotting process. Fibrinogen, a soluble glycoprotein, plays a pivotal role in hemostasis by participating in the formation of blood clots. This process involves the conversion of fibrinogen into insoluble fibrin strands, which form a mesh-like structure that traps blood cells to prevent excessive bleeding. Fibrinogen γ is one of the three polypeptide chains that make up fibrinogen, with the other two being α and β chains. Inhibitors targeting fibrinogen γ are engineered to interfere with its functionality, thus disrupting the formation of stable fibrin clots.
These inhibitors typically work by binding to specific regions or domains on the fibrinogen γ chain, preventing its interaction with other components of the clotting cascade. By doing so, they hinder the conversion of fibrinogen into fibrin and inhibit the formation of a stable blood clot. This class of compounds may have applications in various fields, including research and diagnostics, as they allow for the precise manipulation of blood clotting mechanisms.
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