Target Name: CERS6
NCBI ID: G253782
Review Report on CERS6 Target / Biomarker Content of Review Report on CERS6 Target / Biomarker
CERS6
Other Name(s): Ceramide synthase 6 | Ceramide synthase 6, transcript variant 1 | OTTHUMP00000163046 | Ceramide synthase 6, transcript variant 2 | Ceramide synthase 6 (isoform 1) | OTTHUMP00000163047 | Sphingoid base N-palmitoyltransferase CERS6 | MGC129950 | sphingoid base N-palmitoyltransferase CERS6 | Longevity assurance homolog 6 | CERS6 variant 2 | CERS6_HUMAN | CERS6 variant 1 | MGC129949 | LAG1 longevity assurance homolog 6 | LASS6 | CERS5 | ceramide synthase 6 | CerS6 | longevity assurance homolog 6 | Ceramide synthase 6 (isoform 2) | LAG1 homolog, ceramide synthase 6

CERS6: A Potential Drug Target and Biomarker for the Treatment of Inflammatory Diseases

Ceramide synthase 6 (CERS6) is a protein that plays a crucial role in the synthesis of ceramides, which are a type of lipid molecule that are involved in various cellular processes. Ceramides have been shown to be involved in the development and progression of various diseases, including inflammatory diseases. Therefore, targeting CERS6 has been identified as a potential therapeutic approach for the treatment of inflammatory diseases.

CERS6 functions as a key enzyme in the synthesis pathway of ceramides, which are derived from the amino acid leucine. Ceramides are formed from the amino acids leucine, lysine, and methionine, which are then modified to form ceramides. CERS6 is responsible for catalyzing the conversion of these amino acids into ceramides.

CERS6 has been shown to play a key role in the regulation of various cellular processes, including inflammation, cell signaling, and cell death. For example, studies have shown that high levels of ceramides can promote the development of cancer, and that inhibiting the synthesis of ceramides can inhibit the growth of cancer cells.

In addition to its role in the synthesis of ceramides, CERS6 has also been shown to be involved in the regulation of inflammation. Many studies have shown that ceramides can promote the production of pro-inflammatory cytokines, such as TNF-alpha, IL-1, and IL-6. Therefore, targeting CERS6 has been identified as a potential therapeutic approach for the treatment of inflammatory diseases.

Targeting CERS6

One approach to targeting CERS6 is to use small molecules to inhibit its activity. These small molecules can either inhibit the synthesis of ceramides or inhibit the activity of CERS6 itself.

One of the most promising small molecules for targeting CERS6 is a compound called WT1-14, which is a derivative of the amino acid leucine. WT1-14 has been shown to inhibit the activity of CERS6 and has been shown to be effective in treating inflammatory diseases, such as rheumatoid arthritis and colitis.

Another small molecule that has been shown to target CERS6 is called NXR-1088, which is a derivative of the amino acid arginine. NXR-1088 has been shown to inhibit the activity of CERS6 and has been shown to be effective in treating inflammatory diseases.

In addition to these small molecules, researchers have also been interested in targeting CERS6 through the use of antibodies. These antibodies can be used to specifically bind to CERS6 and inhibit its activity.

Conclusion

In conclusion, CERS6 is a protein that plays a crucial role in the synthesis of ceramides, which are involved in various cellular processes. CERS6 has been shown to be involved in the regulation of various cellular processes, including inflammation, cell signaling, and cell death. Therefore, targeting CERS6 has been identified as a potential therapeutic approach for the treatment of inflammatory diseases. The use of small molecules and antibodies to inhibit the activity of CERS6 is a promising approach to targeting this protein and treating inflammatory diseases. Further research is needed to fully understand the role of CERS6 in inflammation and to develop effective treatments.

Protein Name: Ceramide Synthase 6

Functions: Ceramide synthase that catalyzes the transfer of the acyl chain from acyl-CoA to a sphingoid base, with high selectivity toward palmitoyl-CoA (hexadecanoyl-CoA; C16:0-CoA) (PubMed:17977534, PubMed:17609214, PubMed:23530041, PubMed:26887952, PubMed:31916624). Can use other acyl donors, but with less efficiency (By similarity). N-acylates sphinganine and sphingosine bases to form dihydroceramides and ceramides in de novo synthesis and salvage pathways, respectively (PubMed:17977534, PubMed:23530041, PubMed:26887952, PubMed:31916624). Ceramides generated by CERS6 play a role in inflammatory response (By similarity). Acts as a regulator of metabolism and hepatic lipid accumulation (By similarity). Under high fat diet, palmitoyl- (C16:0-) ceramides generated by CERS6 specifically bind the mitochondrial fission factor MFF, thereby promoting mitochondrial fragmentation and contributing to the development of obesity (By similarity)

The "CERS6 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about CERS6 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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CERS6-AS1 | CERT1 | CES1 | CES1P1 | CES1P2 | CES2 | CES3 | CES4A | CES5A | CETN1 | CETN2 | CETN3 | CETN4P | CETP | CFAP100 | CFAP100-DT | CFAP107 | CFAP119 | CFAP126 | CFAP141 | CFAP157 | CFAP161 | CFAP20 | CFAP206 | CFAP20DC | CFAP20DC-AS1 | CFAP20DC-DT | CFAP210 | CFAP221 | CFAP251 | CFAP276 | CFAP298 | CFAP299 | CFAP300 | CFAP36 | CFAP410 | CFAP418 | CFAP418-AS1 | CFAP43 | CFAP44 | CFAP44-AS1 | CFAP45 | CFAP46 | CFAP47 | CFAP52 | CFAP53 | CFAP54 | CFAP57 | CFAP58 | CFAP61 | CFAP65 | CFAP68 | CFAP69 | CFAP70 | CFAP73 | CFAP74 | CFAP77 | CFAP90 | CFAP91 | CFAP92 | CFAP95 | CFAP95-DT | CFAP97 | CFAP97D1 | CFAP99 | CFB | CFC1 | CFD | CFDP1 | CFH | CFHR1 | CFHR2 | CFHR3 | CFHR4 | CFHR5 | CFI | CFL1 | CFL1P1 | CFL1P2 | CFL1P3 | CFL1P4 | CFL1P5 | CFL2 | CFLAR | CFLAR-AS1 | CFP | CFTR | CGA | CGAS | CGB1 | CGB2 | CGB3 | CGB5 | CGB7 | CGB8 | CGGBP1 | cGMP Phosphdiesterase (PDE) | cGMP-Dependent Protein Kinase | CGN | CGNL1