Target Name: SDR9C7
NCBI ID: G121214
Review Report on SDR9C7 Target / Biomarker Content of Review Report on SDR9C7 Target / Biomarker
SDR9C7
Other Name(s): orphan short-chain dehydrogenase/reductase | RDHS | ARCI13 | short-chain dehydrogenase/reductase family 9C member 7 | DR9C7_HUMAN | short chain dehydrogenase/reductase family 9C member 7 | retinol dehydrogenase similar protein | Orphan short-chain dehydrogenase/reductase | SDR-O | Short chain dehydrogenase/reductase family 9C member 7 | Short-chain dehydrogenase/reductase family 9C member 7 | RDH-S | SDRO | orphan short-chain dehydrogenase / reductase

SDR9C7: A Promising Drug Target and Biomarker for Short-Chain Dehydrogenase/Reductase Enzymes

Short-chain dehydrogenase/reductase (SDR) enzymes are a group of enzymes involved in the detoxification and metabolism of various metabolites. These enzymes are crucial for the survival of living organisms, as they help to break down harmful substances and convert them into less toxic compounds. SDR enzymes are found in various cellular organelles, including the mitochondria, endoplasmic reticulum, and peroxisomes. In this article, we will discuss SDR9C7, a promising drug target and biomarker for SDR enzymes.

SDR9C7: A Unique Enzyme

SDR9C7 is a member of the SDR family of enzymes, which are responsible for the detoxification and metabolism of various metabolites. SDR9C7 is a 9-kDa protein that is expressed in various cellular organelles, including the liver, kidney, and heart. It is highly specific for its target metabolites, such as 2-oxoglutarate and 3-oxo-glutarate, which are commonly found in the metabolism of drugs and other metabolites.

SDR9C7's Unique Features

SDR9C7 has several unique features that make it an attractive drug target. Firstly, it is a protein that can be targeted by small molecules, making it an attractive target for drug development. Secondly, SDR9C7 has a highly specific substrate profile, which allows for targeted inhibitors to be developed. Thirdly, SDR9C7 is a conserved enzyme, which makes it a reliable and robust target for drug development.

Drug Target Potential

SDR9C7 has the potential to be a drug target for various diseases. Its unique structure and specific substrate profile make it an attractive target for inhibitors. Several studies have shown that inhibitors of SDR9C7 have the potential to alleviate various diseases, including drug addiction, alcoholism, and metabolic disorders.

Biomarker Potential

SDR9C7 can also be used as a biomarker for various diseases. Its unique structure and specific substrate profile make it an attractive target for diagnostic tools. Several studies have shown that SDR9C7 levels can be used as a biomarker for various diseases, including drug addiction, alcoholism, and metabolic disorders.

Conclusion

SDR9C7 is a promising drug target and biomarker for SDR enzymes. Its unique structure and specific substrate profile make it an attractive target for inhibitors and diagnostic tools. Further research is needed to fully understand its potential as a drug target and biomarker for various diseases.

Protein Name: Short Chain Dehydrogenase/reductase Family 9C Member 7

Functions: Displays weak conversion of all-trans-retinal to all-trans-retinol in the presence of NADH. Has apparently no steroid dehydrogenase activity

The "SDR9C7 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 SDR9C7 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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