2005
DOI: 10.1016/s1572-5995(05)80036-5
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Biological Activity of Quinones

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Cited by 44 publications
(16 citation statements)
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“…Besides the mentioned compounds, we also detected the naphthoquinones lapachol, α ‐lapachone, naphtho[2,3‐ b ]furan‐4,9‐dione, 2‐isopropyl‐ and avicenol‐C. The naphthoquinones belong to the quinone group, which constitutes a structurally diverse class of phenolic compounds with a wide range of pharmacological properties (Martínez and Benito ). In a review of mangrove plant natural products, Wu et al .…”
Section: Resultsmentioning
confidence: 95%
“…Besides the mentioned compounds, we also detected the naphthoquinones lapachol, α ‐lapachone, naphtho[2,3‐ b ]furan‐4,9‐dione, 2‐isopropyl‐ and avicenol‐C. The naphthoquinones belong to the quinone group, which constitutes a structurally diverse class of phenolic compounds with a wide range of pharmacological properties (Martínez and Benito ). In a review of mangrove plant natural products, Wu et al .…”
Section: Resultsmentioning
confidence: 95%
“…The majority of plant quinones are the relatively simple benzoquinoes, napththoquinones or anthraquinones, e.g., found in the Rubiaceae (anthraquinones), Bignonaceae (napthoquinones) and Plumbaginaceae (benzoquinones) families. 32 …”
Section: Quinonesmentioning
confidence: 99%
“…The binding energies of spinochrome dimers (l " Table 2) are higher than the binding energies of monomers by~2 kcal/mol, however, the dimers do not exactly complement the ligand binding site and bind further from the site up to the flexible loops region. As monomers fit better to the active site (resembling the binding mode of H 1 R antagonist doxepin [14]), they may compete with histamine more effectively than dimers and therefore may be more effective inhibitors than the dimers.…”
Section: Timementioning
confidence: 99%