40110-13-2Relevant academic research and scientific papers
Inhibition of neuronal nitric oxide synthase by 4-amino pteridine derivatives: Structure-activity relationship of antagonists of (6R)-5,6,7,8- tetrahydrobiopterin cofactor
Fr?hlich, Lothar G.,Kotsonis, Peter,Traub, Hermann,Taghavi-Moghadam, Shahriyar,Al-Masoudi, Najim,Hofmann, Heinrich,Strobel, Hartmut,Matter, Hans,Pfleiderer, Wolfgang,Schmidt, Harald H. H. W.
, p. 4108 - 4121 (2007/10/03)
The family of nitric oxide synthases (NOS) catalyzes the conversion of L-arginine to L-citrulline and nitric oxide (NO), an important cellular messenger molecule which has been implicated in the pathophysiology of septic shock and inflammatory and neurode
Synthetic Analogues of Tetrahydrobiopterin with Cofactor Activity for Aromatic Amino Acid Hydroxylases
Bigham, E. C.,Smith, G. K.,Reinhard, J. F.,Mallory, W. R.,Nichol, C. A.,Morrison, R. W.
, p. 40 - 45 (2007/10/02)
Tetrahydrobiopterin (THB) analogues with 6-alkoxymethyl substituents, 3a-j, where the substituents, were straight- and branched-chain alkyl ranging from methyl to octyl, have been synthesized by the Tylor method from pyrazine ortho amino nitriles by guanidine cyclization, hydrolysis in aqueous NaOH, and catalytic hydrogenation over Pt in trifluoroacetic acid (TFA).The best of these compounds, 3b, is an excellent cofactor for phenylalanine hydroxylase, tyrosine hydroxylase (V=154percent of THB), and tryptophan hydroxylase, does not destabilize the binding of substrate (Kmtyr=23 μM), and is recycled by dihydropteridine reductase (V=419percent of THB).The compounds are being evaluated as cofactor replacements in biopterin-deficiency diseases.
Biopterin analogs
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, (2008/06/13)
This invention provides the intermediates of formula II-A below, useful to make the pterin compounds of formula I below. The pterin compounds are used in human and veterinary medicine. STR1 wherein R represents a lower alkyl of 1 to 8 carbons.
