Results 141 to 150 of about 3,922 (190)
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Polarographic Study of Pteridines
Journal of Pharmaceutical Sciences, 1966The electronegativity of the half-wave potentials of a series of pteridine congeners was found to be related to the substituent groups. The 2,4,7-triaminopteridines, 7-substituted 4-amino-2-aryl-6-pteridinecarboxarnides, and 4,7-diamino-2-aryl-6-pteridinecarboxamides were characterized, in that order, by decreasingly lower electronegative half-wave ...
M, Lapidus, M E, Rosenthale
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Nature, 1948
ALTHOUGH many derivatives of pteridine, both natural and synthetic, are known, the parent substance pteridine (I) does not appear to have been described. This substance has now been prepared by the condensation of 4 : 5-diaminopyrimidine with glyoxal bisulphite.
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ALTHOUGH many derivatives of pteridine, both natural and synthetic, are known, the parent substance pteridine (I) does not appear to have been described. This substance has now been prepared by the condensation of 4 : 5-diaminopyrimidine with glyoxal bisulphite.
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Reductone and the Synthesis of Pteridines
Nature, 1948As we have pointed out1 that the 3-carbon atom unit comprising the ring atoms 6 and 7 and the exocyclic carbon atom (indicated in heavy type) in pteroic acid (I) might be derived from a triose, 3-phosphoglyceraldehyde and phosphodihydroxyacetone being specifically mentioned, the suggestion by O‘Meara, McNally and Nelson2 that the strongly reducing non ...
H S, FORREST, J, WALKER
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Pteridines and affective disorders
Acta Neuropsychiatrica, 2002The pteridine tetrahydrobiopterin (BH4) is an essential cofactor in the biosynthesis of dopamine, (nor)epinephrine, serotonin and nitric oxide (NO). Furthermore, BH4 has a direct influence on release mechanisms of these neurotransmitters and on serotonin receptor binding activityimmunology.
Hoekstra, R (Rosa), Fekkes, Durk
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Pteridines as Pigments in Amphibians
Science, 1964Extracts of brightly colored skins from nine amphibian species were analyzed chromatographically. In yellow skin in which xanthophores predominated, relatively large quantities of sepiapterin were found, while in red skin which was laden with erythrophores, three drosopterins were most prevalent.
M, OBIKA, J T, BAGNARA
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Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1975
Summary Over the pH range 1–12, pteridine is reduced at the dropping mercury electrode (DME) and pyrolytic graphite electrode (PGE) by way of three polarographic or voltammetric processes. The first, least negative process, is a reversible 2 e -2H + reduction of pteridine to 5,8-dihydropteridine.
David L. McAllister, Glenn Dryhurst
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Summary Over the pH range 1–12, pteridine is reduced at the dropping mercury electrode (DME) and pyrolytic graphite electrode (PGE) by way of three polarographic or voltammetric processes. The first, least negative process, is a reversible 2 e -2H + reduction of pteridine to 5,8-dihydropteridine.
David L. McAllister, Glenn Dryhurst
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Nature, 1949
THERE is a growing biological interest in derivatives of pteridine (I: R1, R2, R3, R4 = H) as a source of antagonists for folic acid (I: R1 = OH; R2 = NH2 ; R4 = H; R3 = CH2.NH.C6H4.CO.NHCH(COOH): CH2CH2COOH-p), since this vitamin plays an important part in the growth of certain bacteria and normal and malignant tissue.
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THERE is a growing biological interest in derivatives of pteridine (I: R1, R2, R3, R4 = H) as a source of antagonists for folic acid (I: R1 = OH; R2 = NH2 ; R4 = H; R3 = CH2.NH.C6H4.CO.NHCH(COOH): CH2CH2COOH-p), since this vitamin plays an important part in the growth of certain bacteria and normal and malignant tissue.
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Pteridines. IX. Some pteridine isomers of triamterene
Journal of Medicinal Chemistry, 1968J, Weinstock, R Y, Dunoff
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