The term I-309 inhibitors pertains to a diverse group of compounds that influence interactions and signaling of the chemokine I-309 (or CCL1) with its primary receptors, primarily CCR8. I-309, part of the CC chemokine family, plays a key role in immune response regulation by aiding in the recruitment and activation of immune cells like T cells and monocytes. These inhibitors are carefully engineered to interact with precise binding sites on I-309 or its receptors, disrupting their normal interactions. This disruption can potentially impact the complex signaling pathways mediated by I-309, influencing immune cell migration and related processes. Developing I-309 inhibitors combines synthetic chemistry, structural biology, and molecular modeling. Each inhibitor is intricately designed to fit binding site contours on I-309 or its receptors, enabling molecular interactions that lead to inhibitory effects. By intercepting natural interactions between I-309 and its receptors, these inhibitors aim to interrupt the molecular events culminating in immune cell chemotaxis and activation.
Structural diversity characterizes I-309 inhibitors, with various molecular architectures, motifs, and scaffolds. These distinct features act as keys that fit into the molecular locks of the chemokine-receptor binding interface. Binding induces subtle conformational changes in I-309 or the receptor, affecting signal transmission and possibly immune cell activation states. Mechanisms by which these inhibitors function are multifaceted. Some compete with I-309 for receptor binding, blocking chemokine engagement. Others bind to I-309 directly, disrupting its receptor interactions. This interplay enhances our comprehension of chemokine-mediated immune responses and molecular dynamics. I-309 inhibitor research sheds light on the intricate signaling guiding immune cell behavior, offering insights into immune cell trafficking's molecular basis and its implications for regulation and surveillance. Continued exploration of these inhibitors deepens our understanding of immune responses, uncovering the complex mechanisms orchestrating immune cell coordination.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Bis(2-carboxyethylgermanium(IV) sesquioxide) | 12758-40-6 | sc-227361 | 5 g | $76.00 | ||
Also known as Ge-132, this organic germanium compound has been studied for its immunomodulatory effects, which could potentially involve interactions with I-309. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
While primarily known for its role in mTOR pathway inhibition, rapamycin's immunosuppressive effects could indirectly affect I-309-mediated immune responses. | ||||||
BX 471 | 217645-70-0 | sc-507448 | 5 mg | $240.00 | ||
A selective antagonist of CCR1 and CCR8, BX471 has been studied for its potential to inhibit the interaction between I-309 and its receptor. | ||||||
ML 120B Dihydrochloride | 783348-36-7 (free base) | sc-487759 | 5 mg | $380.00 | ||
This compound is another CCR8 antagonist that has been studied for its potential effects on I-309-mediated responses. |