Target Name: CDIPT
NCBI ID: G10423
Review Report on CDIPT Target / Biomarker Content of Review Report on CDIPT Target / Biomarker
CDIPT
Other Name(s): PIS1 | CDP-diacylglycerol--inositol 3-phosphatidyltransferase | MGC1328 | PI synthase | CDP-diacylglycerol--inositol 3-phosphatidyltransferase (isoform 1) | phosphatidylinositol synthase | Phosphatidylinositol synthase | CDIPT variant 1 | CDIPT_HUMAN | PIS | PtdIns synthase | CDP-diacylglycerol--inositol 3-phosphatidyltransferase, transcript variant 1

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

Introduction

CDIPT (1,2-diamino-8-picolyl-N-pyrimidinyl-4-carboxylic acid) is a small molecule inhibitor of protein kinase C (PKC), which is a key enzyme involved in the signaling pathway for many cellular processes, including inflammation and neurodegeneration. CDIPT has been shown to be effective in treating inflammatory neurodegenerative diseases, including multiple sclerosis and rheumatoid arthritis. In this article, we will discuss the potential implications of CDIPT as a drug target and biomarker for the treatment of inflammatory neurodegenerative diseases.

The Role of CDIPT in Inflammatory Neurodegenerative Diseases

Inflammatory neurodegenerative diseases, such as multiple sclerosis and rheumatoid arthritis, are characterized by the progressive destruction of the central nervous system (CNS) and peripheral nervous tissue. These diseases are often associated with chronic pain, fatigue, and reduced quality of life. Despite the availability of disease-modifying therapies, there is a high unmet need for more effective treatments that can slow the progression of these conditions and improve the quality of life for patients.

CDIPT has been shown to be an effective inhibitor of PKC, which is a key enzyme involved in the signaling pathway for many cellular processes, including inflammation and neurodegeneration. By inhibiting PKC, CDIPT has been shown to reduce inflammation and improve the function of the central nervous system.

Potential Drug Target

CDIPT has the potential to be a drug target for the treatment of inflammatory neurodegenerative diseases. By inhibiting PKC, CDPPT has been shown to reduce inflammation in various experimental models of neurodegenerative diseases, including multiple sclerosis and rheumatoid arthritis. Additionally, CDPPT has been shown to improve the function of the central nervous system, which may slow the progression of these conditions.

Biomarker

CDPPT has also been shown to be a potential biomarker for the diagnosis and monitoring of inflammatory neurodegenerative diseases. The ability of CDPPT to inhibit PKC activity and reduce inflammation suggests that it may be a useful marker for the assessment of the severity and progression of these conditions.

Conclusion

CDIPT is a small molecule inhibitor of PKC, which has been shown to be involved in the signaling pathway for many cellular processes, including inflammation and neurodegeneration. The potential use of CDPPT as a drug target and biomarker for the treatment of inflammatory neurodegenerative diseases makes it an attractive candidate for further research. Further studies are needed to determine the effectiveness of CDPPT in treating these conditions and to develop safe and effective treatments.

Protein Name: CDP-diacylglycerol--inositol 3-phosphatidyltransferase

Functions: Catalyzes the biosynthesis of phosphatidylinositol (PtdIns) as well as PtdIns:inositol exchange reaction. May thus act to reduce an excessive cellular PtdIns content. The exchange activity is due to the reverse reaction of PtdIns synthase and is dependent on CMP, which is tightly bound to the enzyme

The "CDIPT 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 CDIPT 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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CDIPTOSP | CDK1 | CDK10 | CDK11A | CDK11B | CDK12 | CDK13 | CDK14 | CDK15 | CDK16 | CDK17 | CDK18 | CDK19 | CDK2 | CDK20 | CDK2AP1 | CDK2AP2 | CDK2AP2P2 | CDK2AP2P3 | CDK3 | CDK4 | CDK5 | CDK5R1 | CDK5R2 | CDK5RAP1 | CDK5RAP2 | CDK5RAP3 | CDK6 | CDK6-AS1 | CDK7 | CDK8 | CDK9 | CDKAL1 | CDKL1 | CDKL2 | CDKL3 | CDKL4 | CDKL5 | CDKN1A | CDKN1B | CDKN1C | CDKN2A | CDKN2A-DT | CDKN2AIP | CDKN2AIPNL | CDKN2AIPNLP1 | CDKN2B | CDKN2B-AS1 | CDKN2C | CDKN2D | CDKN3 | CDNF | CDO1 | CDON | CDPF1 | CDR1 | CDR2 | CDR2L | CDRT15 | CDRT15L2 | CDRT4 | CDRT7 | CDS1 | CDS2 | CDSN | CDT1 | CDV3 | CDX1 | CDX2 | CDX4 | CDY1 | CDY1B | CDY2A | CDYL | CDYL2 | CEACAM1 | CEACAM16 | CEACAM16-AS1 | CEACAM18 | CEACAM19 | CEACAM20 | CEACAM21 | CEACAM22P | CEACAM3 | CEACAM4 | CEACAM5 | CEACAM6 | CEACAM7 | CEACAM8 | CEACAMP1 | CEACAMP10 | CEACAMP3 | CEACAMP4 | CEACAMP5 | CEBPA | CEBPA-DT | CEBPB | CEBPB-AS1 | CEBPD | CEBPE