LPLUNC4, belonging to the PLUNC (Palate, Lung, and Nasal Epithelium Carcinoma Associated) family of proteins, serves a pivotal role in the innate defense mechanisms of the respiratory tract. This group of proteins is secreted predominantly in the nasal, oral, and lung epithelia, contributing to the mucosal immunity by interacting with pathogens, influencing the viscosity and surface properties of mucosal secretions, and possibly exhibiting direct antimicrobial activities. LPLUNC4's function is crucial in maintaining the equilibrium of the respiratory tract's environment, providing a non-specific defense against a wide array of pathogens that constantly challenge the mucosal barriers. The inhibition of LPLUNC4 could lead to compromised mucosal defense, making the respiratory tract more susceptible to infections and the establishment of disease-causing pathogens.
The mechanisms underlying the inhibition of LPLUNC4 can be multifaceted, involving either direct interactions that block the protein's function or indirect pathways that reduce its expression or secretion. Such inhibition could be mediated through the action of specific pathogen-derived enzymes that cleave or otherwise modify LPLUNC4, rendering it inactive. Alternatively, certain pathogens might employ evasion strategies that interfere with the transcriptional regulation of LPLUNC4, leading to reduced protein levels. Furthermore, changes in the microenvironment of the respiratory tract, such as those induced by chronic inflammation or exposure to toxic substances, could negatively affect the expression or stability of LPLUNC4. Understanding the conditions and factors that inhibit LPLUNC4 is essential for elucidating the complex dynamics of host-pathogen interactions and the maintenance of mucosal immunity. Insight into these inhibitory mechanisms could provide valuable information for developing strategies to bolster mucosal defenses and mitigate the risk of respiratory infections.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib is a tyrosine kinase inhibitor that selectively targets BCR-ABL kinase, inhibiting its activity and halting the proliferation of cancer cells in chronic myeloid leukemia (CML). | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $62.00 $112.00 $214.00 $342.00 | 74 | |
Gefitinib is an epidermal growth factor receptor (EGFR) inhibitor that blocks the tyrosine kinase activity of EGFR, thereby impeding cell growth and division in EGFR-mutated lung cancers. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib inhibits multiple kinases, including RAF kinases and VEGFR, which play crucial roles in tumor angiogenesis and cell proliferation, making it effective against various cancers. | ||||||
Vemurafenib | 918504-65-1 | sc-364643 sc-364643A | 10 mg 50 mg | $115.00 $415.00 | 11 | |
Vemurafenib is a selective inhibitor of the BRAF kinase, specifically targeting the V600E-mutated BRAF, suppressing the MAP kinase signaling pathway in melanoma cells. | ||||||
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | $206.00 $299.00 $485.00 | 10 | |
Olaparib is a poly(ADP-ribose) polymerase (PARP) inhibitor, preventing DNA repair in cancer cells with BRCA mutations, leading to genomic instability and cell death. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $153.00 | 5 | |
Ibrutinib is a Bruton's tyrosine kinase (BTK) inhibitor that blocks BTK signaling in B cells, offering effective for B-cell malignancies like CLL and MCL. | ||||||
CH5424802 | 1256580-46-7 | sc-364461 sc-364461A | 5 mg 50 mg | $191.00 $902.00 | ||
CH5424802 is an ALK inhibitor designed to combat ALK-positive non-small cell lung cancer (NSCLC) by targeting ALK kinase, thus inhibiting the oncogenic signaling. | ||||||
Rucaparib | 283173-50-2 | sc-507419 | 5 mg | $150.00 | ||
Rucaparib is another PARP inhibitor that hinders DNA repair processes in cancer cells, particularly effective in ovarian cancer with BRCA mutations. | ||||||
MDV3100 | 915087-33-1 | sc-364354 sc-364354A | 5 mg 50 mg | $240.00 $1030.00 | 7 | |
Enzalutamide acts as a potent androgen receptor inhibitor, disrupting androgen signaling pathways in prostate cancer cells, thereby inhibiting their growth. | ||||||
ABT-199 | 1257044-40-8 | sc-472284 sc-472284A sc-472284B sc-472284C sc-472284D | 1 mg 5 mg 10 mg 100 mg 3 g | $116.00 $330.00 $510.00 $816.00 $1632.00 | 10 | |
ABT-199 is a selective B-cell lymphoma-2 (BCL-2) inhibitor that promotes apoptosis in B-cell malignancies by blocking the anti-apoptotic effects of BCL-2 proteins. | ||||||