Target Name: ADRA1B
NCBI ID: G147
Review Report on ADRA1B Target / Biomarker Content of Review Report on ADRA1B Target / Biomarker
ADRA1B
Other Name(s): ALPHA1BAR | ADA1B_HUMAN | Alpha-1B-adrenergic receptor | Alpha1B-adrenoceptor | Alpha1B-adrenergic receptor | Adrenoceptor alpha 1B | adrenergic, alpha-1B-, receptor | Alpha-1B adrenergic receptor | alpha-1B adrenoreceptor | adrenoceptor alpha 1B | Alpha-1B adrenoreceptor | ADRA1 | alpha-1B adrenoceptor | Alpha-1B adrenoceptor

Exploring the Potential Drug Target and Biomarker ADRA1B1B

Alzheimer's disease is a neurodegenerative disorder that affects millions of people worldwide, leading to progressive memory loss, decline in cognitive function, and ultimately, death. The underlying cause of Alzheimer's disease is the accumulation of neurofibrillary tangles and senile plaques within the brain. While several treatments have been developed to manage the symptoms, there is still no cure for Alzheimer's disease. Therefore, drug targeting and biomarker discovery are critical areas of research to find new treatments and improve the treatment outcomes.

ADRA1B1B: A Potential Drug Target and Biomarker

The Alzheimer's disease is caused by the accumulation of neurofibrillary tangles and senile plaques within the brain. These tangles and plaques contain abnormal aggregates of the protein tau and beta-amyloid, respectively, which cause neurodegeneration. The production of these tangles and plaques is activated by various factors, including neuroinflammation, oxidative stress, and metabolic imbalances.

One of the potential drug targets in the treatment of Alzheimer's disease is ADRA1B1B, a gene that encodes the protein alpha-synuclein (伪-syn), which is a key protein in the formation of neurofibrillary tangles and senile plaques. The accumulation of 伪-synuclein in the brain is believed to contribute to the development and progression of Alzheimer's disease.

The Potential Role of ADRA1B1B in Alzheimer's Disease Treatment

The drug targeting of ADRA1B1B is based on the inhibition of its encoded protein, alpha-synuclein (伪-syn), which is involved in the formation of neurofibrillary tangles and senile plaques. Several studies have shown that the 伪-syn protein is overexpressed in the brains of people with Alzheimer's disease, and that the levels of 伪-syn in the brain are directly proportional to the severity of the disease. Therefore, targeting 伪-syn with drugs that can inhibit its accumulation in the brain may be an effective way to treat Alzheimer's disease.

One of the potential drugs that can target 伪-syn is tau-targeted small molecule inhibitors, which have been shown to be effective in treating other neurodegenerative disorders, such as Parkinson's disease and frontotemporal dementia. These inhibitors work by binding to the alpha-syn protein and preventing its accumulation in the brain.

Another potential drug that can target 伪-syn is aducanumab, a monoclonal antibody that targets the alpha-syn protein. Aducanumab has been shown to be effective in preclinical studies in treating Alzheimer's disease, and is currently being evaluated in clinical trials.

The Potential Role of ADRA1B1B as a Biomarker

The diagnosis of Alzheimer's disease is based on the presence of certain hallmark clinical features, such as progressive memory loss, decline in cognitive function, and behavioral changes. While these symptoms can provide valuable information for the diagnosis of the disease, they are not always reliable indicators of its severity. Therefore, the development of biomarkers that can be used to measure the level of 伪-syn in the brain may be an important step in the development of new treatments for Alzheimer's disease.

One of the potential biomarkers for Alzheimer's disease is the level of 伪-syn in the brain. Studies have shown that the level of 伪-syn in the brain is directly proportional to the severity of the disease. Therefore, measuring the level of 伪-syn in the brain may be an effective way to diagnose Alzheimer's disease and monitor the effectiveness of different treatments.

Another potential biomarker for

Protein Name: Adrenoceptor Alpha 1B

Functions: This alpha-adrenergic receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. Its effect is mediated by G(q) and G(11) proteins. Nuclear ADRA1A-ADRA1B heterooligomers regulate phenylephrine (PE)-stimulated ERK signaling in cardiac myocytes

The "ADRA1B 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 ADRA1B 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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