4-phenylbutyric acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 2 studies
4-phenylbutyric acid: RN refers to the parent cpd
4-phenylbutyric acid : A monocarboxylic acid the structure of which is that of butyric acid substituted with a phenyl group at C-4. It is a histone deacetylase inhibitor that displays anticancer activity. It inhibits cell proliferation, invasion and migration and induces apoptosis in glioma cells. It also inhibits protein isoprenylation, depletes plasma glutamine, increases production of foetal haemoglobin through transcriptional activation of the gamma-globin gene and affects hPPARgamma activation.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Armstrong, AJ | 1 |
| Henke, BR | 1 |
| Collado, MS | 1 |
| Taylor, JM | 1 |
| Pourtaheri, TD | 1 |
| Dillberger, JE | 1 |
| Roper, TD | 1 |
| Wamhoff, BR | 1 |
| Olson, MW | 1 |
| Figler, RA | 1 |
| Hoang, SA | 1 |
| Reardon, JE | 1 |
| Johns, BA | 1 |
2 other studies available for 4-phenylbutyric acid and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Identification of 2,2-Dimethylbutanoic Acid (HST5040), a Clinical Development Candidate for the Treatment of Propionic Acidemia and Methylmalonic Acidemia.
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Animals; Area Under Curve; Butyrates; Cells, | 2021 |
Sodium phenylbutyrate for urea cycle enzyme deficiencies.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Costs and Cost Analysis; Female; Humans; Infant; Liver; | 1996 |