Target Name: CYP20A1
NCBI ID: G57404
Review Report on CYP20A1 Target / Biomarker Content of Review Report on CYP20A1 Target / Biomarker
CYP20A1
Other Name(s): Cytochrome P450, family 20, subfamily A, polypeptide 1 | CYP20A1 variant 2 | MGC22229 | Cytochrome P450 family 20 subfamily A member 1, transcript variant 2 | cytochrome P450, family 20, subfamily A, polypeptide 1 | cytochrome P450 monooxygenase | Cytochrome P450 monooxygenase | OTTHUMP00000206151 | CYP-M | Cytochrome P450 20A1 | cytochrome P450 family 20 subfamily A member 1 | CP20A_HUMAN | Cytochrome P450 20A1 (isoform 2)

CYP20A1: A Potent Drug Target for Cancer and Neurodegenerative Diseases

CYP20A1, also known as Cytochrome P450 (CYP) 20A1, is a member of the cytochrome P450 family 20 and is located in the subfamily A. It is a polypeptide with 183 amino acid residues and has a calculated molecular weight of 21 kDa. CYP20A1 is expressed in various tissues and cells in the body, including the liver, lung, and brain, and is involved in the metabolism of a wide variety of drugs, including statins, thiopurine drugs, and benzodiazepines.

CYP20A1 is a potent enzyme and has been shown to catalyze the metabolism of many drugs with a wide range of chemical structures. It is highly specific for its substrates, and is able to convert a wide variety of molecules into their metabolites with high efficiency. CYP20A1 is also known for its role in drug metabolism in humans, as it is often used as a biomarker to monitor the effectiveness of anticancer drugs.

One of the unique features of CYP20A1 is its expression in the brain, where it is highly concentrated and is involved in the metabolism of a wide variety of drugs that are harmful to the brain, including chemotherapy drugs, antipsychotic drugs, and many others. This makes CYP20A1 an attractive target for drug developers, as it can be used to study the metabolism of drugs in the brain and to develop new treatments for conditions such as cancer and neurodegenerative diseases.

Another promising aspect of CYP20A1 is its potential as a drug target for cancer. Many anti-cancer drugs work by inhibiting the activity of CYP20A1, leading to reduced levels of metabolites that can be toxic to cancer cells. By blocking the activity of CYP20A1, these drugs can spare healthy cells from damage and increase the overall effectiveness of the treatments. Additionally, CYP20A1 has also been shown to be involved in the metabolism of neurotransmitters, which are involved in the regulation of many important cellular processes, including mood, pain, and sleep. This suggests that CYP20A1 may also be a useful target for the treatment of neurodegenerative diseases.

CYP20A1 is also an important enzyme in the metabolism of many other drugs that are used to treat a wide range of medical conditions. For example, it is often used to metabolize statins, which are used to treat high cholesterol levels. CYP20A1 has also been shown to play a role in the metabolism of thiopurine drugs, which are used to treat autoimmune disorders and other conditions. Additionally, CYP20A1 is often used to metabolize benzodiazepines, which are used to treat anxiety and other mood disorders.

In conclusion, CYP20A1 is a highly versatile enzyme that is involved in the metabolism of a wide variety of drugs. Its expression in various tissues and its ability to convert a wide range of molecules into their metabolites make it an attractive target for drug developers. The studies of CYP20A1 have shown that it is a powerful predictor of the metabolism of drugs and that it can be used to study the effects of drugs on the brain. Furthermore, its involvement in the metabolism of many drugs that are used to treat cancer and neurodegenerative diseases makes it an attractive target for drug developers.

Protein Name: Cytochrome P450 Family 20 Subfamily A Member 1

The "CYP20A1 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 CYP20A1 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

More Common Targets

CYP21A1P | CYP21A2 | CYP24A1 | CYP26A1 | CYP26B1 | CYP26C1 | CYP27A1 | CYP27B1 | CYP27C1 | CYP2A13 | CYP2A6 | CYP2A7 | CYP2A7P1 | CYP2B6 | CYP2B7P | CYP2C18 | CYP2C19 | CYP2C61P | CYP2C8 | CYP2C9 | CYP2D6 | CYP2D7 | CYP2D8P | CYP2E1 | CYP2F1 | CYP2F2P | CYP2G1P | CYP2J2 | CYP2R1 | CYP2S1 | CYP2T1P | CYP2U1 | CYP2U1-AS1 | CYP2W1 | CYP39A1 | CYP3A4 | CYP3A43 | CYP3A5 | CYP3A51P | CYP3A7 | CYP3A7-CYP3A51P | CYP3AP2 | CYP46A1 | CYP4A11 | CYP4A22 | CYP4B1 | CYP4F11 | CYP4F12 | CYP4F2 | CYP4F22 | CYP4F26P | CYP4F29P | CYP4F3 | CYP4F30P | CYP4F34P | CYP4F35P | CYP4F59P | CYP4F62P | CYP4F8 | CYP4V2 | CYP4X1 | CYP4Z1 | CYP4Z2P | CYP51A1 | CYP51A1-AS1 | CYP51A1P1 | CYP51A1P2 | CYP51A1P3 | CYP7A1 | CYP7B1 | CYP8B1 | CYREN | CYRIA | CYRIB | CYS1 | CYSLTR1 | CYSLTR2 | CYSRT1 | Cysteine Protease | CYSTM1 | CYTB | CYTH1 | CYTH2 | CYTH3 | CYTH4 | CYTIP | CYTL1 | Cytochrome b5 reductase | Cytochrome bc1 complex | Cytochrome c oxidase | Cytochrome P450 1A (CYP1A) | Cytochrome P450 26 | Cytochrome P450 3A (CYP3A) | Cytochrome P450 4A | Cytochrome P450 Enzymes | Cytohesin | Cytoplasmatic dynein | Cytoplasmic dynein complex | CYTOR | CYYR1