CAS 948-60-7
:Pterin-6-carboxylic acid
- 2-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid
- 2-Amino-4-hydroxy-6-carboxypteridine
- 2-Amino-4-hydroxypteridine-6-carboxylic acid
- 2-Amino-4-hydroxypterin-6-carboxylic acid
- 2-Amino-4-oxo-1,4-dihydropteridine-6-carboxylic acid
- 2-Amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid
- 2-Amino-4-oxo-4,8-dihydropteridine-6-carboxylic acid
- 2-Amino-6-carboxy-4-hydroxypteridine
- 2-Imino-4-oxo-1,2,3,4-tetrahydropteridine-6-carboxylic acid
- 6-Carboxypterin
- 6-Pteridinecarboxylic acid, 2-amino-1,4-dihydro-4-oxo-
- 6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo-
- 6-Pteridinecarboxylic acid, 2-amino-4-hydroxy-
- NSC 96893
- Pterin-6-Carboxylic Acid
- See more synonyms
6-Pteridinecarboxylic acid, 2-amino-3,4-dihydro-4-oxo-
CAS:Formula:C7H5N5O3Purity:98%Color and Shape:SolidMolecular weight:207.1463Pterine-6-carboxylic acid
CAS:6-Carboxypterin, a folic acid breakdown product, is used to research UVA-induced DNA damage.Formula:C7H5N5O3Purity:98%Color and Shape:SolidMolecular weight:207.152-Amino-4-oxo-3,4-dihydropteridine-6-carboxylic acid
CAS:2-Amino-4-oxo-3,4-dihydropteridine-6-carboxylic acidPurity:97%Molecular weight:207.15g/molPterine-6-carboxylic Acid
CAS:Controlled ProductApplications Pterine-6-carboxylic Acid is a degradation product of Folic acid (F680300).
References Akhtar, M., et al.: J. Pharm. Biomed. Anal., 19, 269 (1999), Andrisano, V., et al.: J. Pharm. Biomed. Anal., 32, 983 (2003), Patro, B., et al.: Bioorg. Med. Chem. Lett., 15, 67 (2005),Formula:C7H5N5O3Color and Shape:NeatMolecular weight:207.152-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid
CAS:2-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid is an analytical reagent that reacts with the hydroxyl group of malonic acid to produce a fluorescent derivative. 2-Amino-3,4-dihydro-4-oxo-6-pteridinecarboxylic acid is used in wastewater treatment to measure the effectiveness of the process. The compound reacts with human serum proteins to form a stable complex and can be used as a response element in an analysis matrix. It has been shown that 2 amino 3,4 dihydro 4 oxo 6 pteridine carboxylic acid fluoresces when irradiated by radiation. The optimum pH for this reaction is 7.5 and the reaction mechanism involves formation of a cyclic intermediate followed by cleavage of the C=C bond to release free radicals. Malonic acid is not required for this reaction but it
Formula:C7H5N5O3Purity:Min. 95%Color and Shape:PowderMolecular weight:207.15 g/mol








