2-Amino-4-hydroxypteridine

CAS : 2236-60-4

Ref. 3D-FA12181

Informations sur le produit

• Nom: 2-Amino-4-hydroxypteridine
• Synonymes: Pterin, 2-Amino-1,4-dihydropteridin-4-one, 2-Amino-3,4-dihydropteridin-4-one, 2-Amino-4(1H)-pteridinone, 2-Amino-4(3H)-pteridinone, 2-Amino-4,8-dihydropteridin-4-one, 2-Amino-4-Hydroxy-1H-Pteridine, 2-Amino-4-oxopteridine, 2-Amino-4-pteridone, 2-Aminopteridin-4-ol, 2-Aminopteridin-4-one, 2-amino-5,8-dihydropteridin-4(3H)-one, 2-aminopteridin-4(1H)-one, 4(1H)-Pteridinone, 2-amino-, 4(3H)-Pteridinone, 2-amino-, 4-Oxo-2-aminopteridine, 4-Oxopterin, Nsc 11540, Nsc 170929, Nsc 18696, Pteridoxamine, Pterin (VAN), Pterine, Quinonoid dihydropterin, 2-amino-

Description

2-Amino-4-hydroxypteridine is a chemical compound that is used in the synthesis of other organic compounds. 2-Amino-4-hydroxypteridine binds to molybdenum and coordinates with it through hydrogen bonding, which stabilizes the molecule. The binding between 2-amino-4-hydroxypteridine and molybdenum has been shown to be essential for its antimicrobial activity. This compound inhibits bacterial growth by inhibiting the biosynthesis of monoamine neurotransmitters, such as dopamine and serotonin.
2-Amino-4-hydroxypteridine also inhibits enzyme activities, such as those involved in energy metabolism, as well as structural analysis of nitrogen containing molecules.
The reaction mechanism of 2 amino 4 hydroxypteridine is not well understood, but it has been proposed that this compound reacts with electron acceptors such as oxygen or nitric oxide to form an excited state

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 163.14 g/mol
• Formule: C₆H₅N₅O
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C6H5N5O/c7-6-10-4-3(5(12)11-6)8-1-2-9-4/h1-2H,(H3,7,9,10,11,12)
• Code InChI: InChIKey=HNXQXTQTPAJEJL-UHFFFAOYSA-N
• SMILES: Nc1nc(O)c2nccnc2n1