1987
DOI: 10.1007/978-3-7091-6971-1_1
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Pigments of Fungi (Macromycetes)

Abstract: For Abstract see ChemInform Abstract in Full Text.

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Cited by 131 publications
(53 citation statements)
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“…It is worth noting here that previously reported terphenyl metabolites having a para-quinone core, like the flavomentins AϪD from Paxillus atrotomentosus and P. panuoides, are orange pigments, while ortho-quinones, like the spiromentins AϪD [18] from P. atrotomentosus, or the hydroxylated phlebiarubrone derivatives from Phlebia strigosozonata, are violet pigments. [19] The λ max values in the UV-Vis spectrum of the pigment are very close to those of spiromentins AϪD and phlebiarubrone derivatives. [19] All these data strongly suggest that the structures of the constituents in the mixture of epimeric ortho-quinones are related to sarcodonins and episarcodonins, namely sarcoviolin α (10) and episarcoviolin α (11).…”
Section: Introductionmentioning
confidence: 84%
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“…It is worth noting here that previously reported terphenyl metabolites having a para-quinone core, like the flavomentins AϪD from Paxillus atrotomentosus and P. panuoides, are orange pigments, while ortho-quinones, like the spiromentins AϪD [18] from P. atrotomentosus, or the hydroxylated phlebiarubrone derivatives from Phlebia strigosozonata, are violet pigments. [19] The λ max values in the UV-Vis spectrum of the pigment are very close to those of spiromentins AϪD and phlebiarubrone derivatives. [19] All these data strongly suggest that the structures of the constituents in the mixture of epimeric ortho-quinones are related to sarcodonins and episarcodonins, namely sarcoviolin α (10) and episarcoviolin α (11).…”
Section: Introductionmentioning
confidence: 84%
“…[19] The λ max values in the UV-Vis spectrum of the pigment are very close to those of spiromentins AϪD and phlebiarubrone derivatives. [19] All these data strongly suggest that the structures of the constituents in the mixture of epimeric ortho-quinones are related to sarcodonins and episarcodonins, namely sarcoviolin α (10) and episarcoviolin α (11). As further confirmation, the mixture of 10 and 11 was subjected to reductive acetylation with Zn/Ac 2 O, according to a standard procedure for fungal terphenylquinones.…”
Section: Introductionmentioning
confidence: 84%
“…Terphenyl is a common structural motif found in various natural products, largely isolated from microbes and mushrooms [1]. In recent years, it has been reported that some terphenyls exhibit considerable biological activities, for example, potent anticoagulants, immunosuppressants, antithrombotic, neuroprotective, specific 5-lipoxygenase inhibitory, and cytotoxic activities [2].…”
Section: Introductionmentioning
confidence: 99%
“…Terphenyl is a common structural motif found in various natural products, largely isolated from microbes and mushrooms [1]. In recent years, it has been reported that some terphenyls exhibit significant biological activities, e.g., potent anticoagulant, immunosuppressants, antithrombotic, neuroprotective, specific 5-lipoxygenase inhibitory and cytotoxic activities [2].…”
Section: Introductionmentioning
confidence: 99%