Ly49F inhibitors are a class of chemical compounds that target the Ly49F receptor, a specific member of the Ly49 receptor family found predominantly in natural killer (NK) cells. The Ly49 receptors are a group of C-type lectin-like receptors that are primarily responsible for regulating the activity of NK cells through recognition of major histocompatibility complex class I (MHC-I) molecules. Ly49F, in particular, binds to certain MHC-I molecules, transmitting signals that influence NK cell function, either activating or inhibiting their cytotoxic responses. The precise modulation of this receptor can be crucial for controlling the immune response, especially in the context of maintaining the delicate balance between immune activation and inhibition. Inhibitors of Ly49F can disrupt this signaling process, potentially affecting NK cell recognition of cellular targets, leading to altered immune surveillance and interaction dynamics.
Chemically, Ly49F inhibitors are designed to bind specifically to the Ly49F receptor, interfering with its ability to interact with MHC-I molecules. This can be achieved through various structural motifs that target the receptor's binding domain, hindering its conformation and function. Some inhibitors might mimic the natural ligands of Ly49F, thereby competitively inhibiting the receptor's activity, while others could bind allosterically, causing conformational changes that affect the receptor's behavior. The development of these inhibitors involves understanding the three-dimensional structure of Ly49F, as well as its ligand-binding affinities, to create molecules that can selectively interfere with its function. Such inhibitors provide a valuable tool for studying the intricacies of receptor-ligand interactions and the broader implications of NK cell regulation within immunological contexts. The specificity and design of Ly49F inhibitors are closely linked to their molecular architecture and the precise targeting of receptor sites to ensure selective modulation of immune pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
ATRA may inhibit KLRK1 expression by modulating immune cell differentiation and influencing the expression of immune surveillance receptors like NKG2D. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
PD-0332991 is suggested to inhibit KLRK1 expression by affecting cell cycle progression, potentially impacting the proliferation and expression of immune cells bearing NKG2D. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB202190 may inhibit KLRK1 expression by modulating the MAPK signaling pathway, potentially influencing the expression and activation of NKG2D on immune cells. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 could potentially inhibit KLRK1 expression by modulating the JNK signaling pathway, potentially impacting the expression and function of NKG2D on immune cells. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 may inhibit KLRK1 expression by affecting the PI3K/AKT signaling pathway, potentially influencing the expression and activation of NKG2D on immune cells. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is suggested to inhibit KLRK1 expression by affecting the PI3K signaling pathway, potentially impacting the expression and function of NKG2D on immune cells. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin may inhibit KLRK1 expression by modulating the mTOR signaling pathway, potentially influencing the expression and activation of NKG2D on immune cells. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
U0126 could potentially inhibit KLRK1 expression by modulating the MAPK/ERK signaling pathway, potentially impacting the expression and function of NKG2D on immune cells. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib is suggested to inhibit KLRK1 expression by affecting the ubiquitin-proteasome pathway, potentially impacting the expression and function of NKG2D on immune cells. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $80.00 $212.00 $408.00 | 48 | |
SB431542 may inhibit KLRK1 expression by modulating the TGF-β signaling pathway, potentially influencing the expression and activation of NKG2D on immune cells. | ||||||