Comprehensive Heterocyclic Chemistry III 2008
DOI: 10.1016/b978-008044992-0.00918-4
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Bicyclic 6-6 Systems: Pteridines

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Cited by 6 publications
(11 citation statements)
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“…1 Analgesic, anti-inflammatory, anticonvulsant, sedative-hypnotic, anti-histaminic, anti-hypertensive, anti-tumor, anti-microbial, ischemia or reperfusion surgery, and anti-parasite activity are some of the pharmacological responses ascribed to these systems. 2 This diversity in the pharmacological action contours of pteridine has piqued the interest of medicinal chemists in exploring this fused Heterocycle's potential against a wide range of activities.…”
Section: Introductionmentioning
confidence: 99%
“…1 Analgesic, anti-inflammatory, anticonvulsant, sedative-hypnotic, anti-histaminic, anti-hypertensive, anti-tumor, anti-microbial, ischemia or reperfusion surgery, and anti-parasite activity are some of the pharmacological responses ascribed to these systems. 2 This diversity in the pharmacological action contours of pteridine has piqued the interest of medicinal chemists in exploring this fused Heterocycle's potential against a wide range of activities.…”
Section: Introductionmentioning
confidence: 99%
“…Naturally occurring pteridines fall into two structural categories: pterins ( 2 ), with a C-2 amino group and a carbonyl group at the C-4 position, and lumazines ( 3 ), with carbonyl groups at both the C-2 and C-4 positions . Although tautomerism is expected for both pterins ( 2 ) and lumazines ( 3 ) as a result of intramolecular proton transfer, it has been demonstrated by spectroscopic and crystallographic studies that, in the most prominent tautomeric species of natural pteridines, the ring nitrogen adopts the thermodynamically more stable lactam configuration, as represented by structures 2 and 3 . …”
Section: Introductionmentioning
confidence: 99%
“…Parallel with these synthetic efforts, the discovery of natural pteridine compounds began in 1889, when Sir Frederick Hopkins reported the isolation of the yellow pigments xanthopterin ( 5 ) and leucopterin ( 6 ) from the wings of the common brimstone butterfly ( Gonepterix rhamni ) and the cabbage butterfly ( Pieris rapae ), respectively . The structures of pterins 5 and 6 were not confirmed until 1940; since then, much work has been directed toward the isolation of new natural pteridines and the investigation of their biological roles. , Most naturally occurring pteridines belong to the pterin family, and some of these pterins possess important biological properties including antitumor, antimicrobial, and antiviral activity, as well as being cofactors in enzymatic reactions. , Thus far, reviews of the reactivity, synthesis, isolation, and bioactivity of pteridines have focused on natural pterins and their analogues rather than lumazines. , …”
Section: Introductionmentioning
confidence: 99%
“…Nonetheless, other approaches are based on the linkage of a pteridine derivative to metal complexes or to molecules known to inhibit a specific target, with the objective of increasing their potency by targeting two different enzymes. Nevertheless, since chemical synthesis of pteridine derivatives is not the focus of this review, information about synthetic methods explaining how pteridine‐based compounds and drug candidates have been developed can be found in the comprehensive reviews by Suckling et al…”
Section: Introductionmentioning
confidence: 99%