4-(dicyanomethylene)-2-methyl-6-(4-(dimethylamino)styryl)-4h-pyran has been researched along with Phenylketonurias in 1 studies
*Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952). [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Banerjee, P; Banik, D; Dutta, R; Kundu, S; Sarkar, N | 1 |
1 other study(ies) available for 4-(dicyanomethylene)-2-methyl-6-(4-(dimethylamino)styryl)-4h-pyran and Phenylketonurias
| Article | Year |
|---|---|
Inhibition of Fibrillar Assemblies of l-Phenylalanine by Crown Ethers: A Potential Approach toward Phenylketonuria.
Topics: Amyloid; Circular Dichroism; Crown Ethers; Kinetics; Microscopy, Confocal; Microscopy, Electron, Scanning; Microscopy, Fluorescence; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Phenylalanine; Phenylketonurias; Proton Magnetic Resonance Spectroscopy; Pyrans; Styrenes | 2016 |