Target Name: FCN3
NCBI ID: G8547
Other Name(s): H-ficolin | HAKA1 | FCN3 variant 1 | OTTHUMP00000006339 | MGC22543 | Ficolin 3, transcript variant 1 | Collagen/fibrinogen domain-containing protein 3 | ficolin 3 | FCN3_HUMAN | FCNH | Ficolin-3 | Collagen/fibrinogen domain-containing lectin 3 p35 | Hakata antigen | ficolin (collagen/fibrinogen domain containing) 3 (Hakata antigen) | collagen/fibrinogen domain-containing protein 3 | OTTHUMP00000006338 | collagen/fibrinogen domain-containing lectin 3 p35

A Promising Drug Target: FCN3 for Various Diseases

FCN3 (H-ficolin), a derivative of the natural compound present in various fruits and vegetables, has been found to be a potential drug target and biomarker in various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. Its unique chemical structure and Biological activity makes it an attractive target for drug development due to its potential to modulate cellular processes and pathways involved in these diseases.

The H-ficolin compound is derived from the plant Fagopyrum glabrum, which is commonly used in traditional medicine for various purposes, including as a spice, a medicine, and a food. The active ingredient of Fagopyrum glabrum is known as fagotrieverin, which is a flavonoid compound that has been shown to have various health benefits, including anti-inflammatory, antioxidant, and anti-cancer effects.

FCN3, as a derivative of fagotrieverin, has been shown to have similar biological activities. FCN3 has been shown to have potent anti-inflammatory effects, and it has been found to reduce the expression of pro-inflammatory genes in various cell types, including human immune cells and neuroblasts. Additionally, FCN3 has been shown to have antioxidant properties, as it has the ability to scavenge free radicals and prevent them from harming cellular components.

The potential drug target of FCN3 is its role in the regulation of cellular processes and pathways involved in various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. One of the primary targets of FCN3 is the regulation of the immune system, as it has been shown to have anti-tumor effects in various cancer cell types.

FCN3 has been shown to inhibit the activation and proliferation of cancer cells, including breast, ovarian, and colorectal cancer cells. Additionally, FCN3 has been shown to enhance the effectiveness of chemotherapy by reducing the sensitivity of cancer cells to the chemotherapy drug. These findings. suggest that FCN3 may be an effective drug target for cancer treatment.

Another potential drug target of FCN3 is its role in the regulation of neurodegenerative disorders. FCN3 has been shown to protect against neurodegenerative disorders caused by various factors, including oxidative stress, inflammation, and neurotoxins.

For example, FCN3 has been shown to protect against neurodegenerate disorders caused by glutamate excitotoxicity, a common cause of neurodegenerative disorders. Additionally, FCN3 has been shown to protect against neurotoxins, such as cadmium and lead, which are known to cause neurodegenerative disorders.

FCN3 may also be a potential drug target for autoimmune diseases, as it has been shown to have anti-inflammatory and anti-allergic effects. For example, FCN3 has been shown to reduce the expression of pro-inflammatory genes inTh2 cells, which are a common cause of autoimmune diseases. Additionally, FCN3 has been shown to enhance the production of regulatory T cells, which may help to dampen the immune response and reduce the development of autoimmune diseases.

In conclusion, FCN3 is a promising drug target and biomarker due to its unique chemical structure and its potential to modulate cellular processes and pathways involved in various diseases, including cancer, neurodegenerative disorders, and autoimmune diseases. Further research is needed to fully understand the biological activities and potential drug targets of FCN3, as well as its potential as a therapeutic agent.

Protein Name: Ficolin 3

Functions: May function in innate immunity through activation of the lectin complement pathway. Calcium-dependent and GlcNAc-binding lectin. Has affinity with GalNAc, GlcNAc, D-fucose, as mono/oligosaccharide and lipopolysaccharides from S.typhimurium and S.minnesota

More Common Targets

FCRL1 | FCRL2 | FCRL3 | FCRL4 | FCRL5 | FCRL6 | FCRLA | FCRLB | FCSK | FDCSP | FDFT1 | FDPS | FDPSP2 | FDPSP4 | FDPSP5 | FDPSP6 | FDPSP7 | FDX1 | FDX2 | FDXACB1 | FDXR | FECH | FEM1A | FEM1AP4 | FEM1B | FEM1C | FEN1 | FENDRR | FER | FER1L4 | FER1L5 | FER1L6 | FER1L6-AS1 | FER1L6-AS2 | FERD3L | FERMT1 | FERMT2 | FERMT3 | Ferritin | FES | Fetal Hemoglobin (HbF) | FETUB | FEV | FEZ1 | FEZ2 | FEZF1 | FEZF1-AS1 | FEZF2 | FFAR1 | FFAR2 | FFAR3 | FFAR4 | FGA | FGB | FGD1 | FGD2 | FGD3 | FGD4 | FGD5 | FGD5-AS1 | FGD5P1 | FGD6 | FGF1 | FGF10 | FGF10-AS1 | FGF11 | FGF12 | FGF12-AS2 | FGF13 | FGF13-AS1 | FGF14 | FGF14-AS1 | FGF14-AS2 | FGF14-IT1 | FGF16 | FGF17 | FGF18 | FGF19 | FGF2 | FGF20 | FGF21 | FGF22 | FGF23 | FGF3 | FGF4 | FGF5 | FGF6 | FGF7 | FGF7P3 | FGF7P5 | FGF7P6 | FGF8 | FGF9 | FGFBP1 | FGFBP2 | FGFBP3 | FGFR1 | FGFR1OP2 | FGFR2 | FGFR3