Date published: 2025-12-19

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LPLUNC4 Inhibitors

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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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$25.00
$117.00
$209.00
27
(1)

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

184475-35-2sc-202166
sc-202166A
sc-202166B
sc-202166C
100 mg
250 mg
1 g
5 g
$62.00
$112.00
$214.00
$342.00
74
(2)

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

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

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

918504-65-1sc-364643
sc-364643A
10 mg
50 mg
$115.00
$415.00
11
(1)

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

763113-22-0sc-302017
sc-302017A
sc-302017B
250 mg
500 mg
1 g
$206.00
$299.00
$485.00
10
(1)

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

936563-96-1sc-483194
10 mg
$153.00
5
(0)

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

1256580-46-7sc-364461
sc-364461A
5 mg
50 mg
$191.00
$902.00
(0)

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

283173-50-2sc-507419
5 mg
$150.00
(0)

Rucaparib is another PARP inhibitor that hinders DNA repair processes in cancer cells, particularly effective in ovarian cancer with BRCA mutations.

MDV3100

915087-33-1sc-364354
sc-364354A
5 mg
50 mg
$240.00
$1030.00
7
(1)

Enzalutamide acts as a potent androgen receptor inhibitor, disrupting androgen signaling pathways in prostate cancer cells, thereby inhibiting their growth.

ABT-199

1257044-40-8sc-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
(0)

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.