1989
DOI: 10.1016/b978-0-12-461011-8.50019-6
|View full text |Cite
|
Sign up to set email alerts
|

Quinones

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
11
0

Year Published

1994
1994
2020
2020

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 17 publications
(12 citation statements)
references
References 169 publications
0
11
0
Order By: Relevance
“…To a lesser extent, this substitution pattern has also been found in other genera of the Rubiaceae, such as Galium (Koyama et al, 1993) and Morinda (Leistner, 1973a). Normally this pattern is typical of AQs derived from acetyl-CoA via the polyketide pathway (Van den Berg and Labadie, 1989). However, the AQs in Cinchona are considered to be of the Rubia type.…”
Section: Introductionmentioning
confidence: 78%
See 1 more Smart Citation
“…To a lesser extent, this substitution pattern has also been found in other genera of the Rubiaceae, such as Galium (Koyama et al, 1993) and Morinda (Leistner, 1973a). Normally this pattern is typical of AQs derived from acetyl-CoA via the polyketide pathway (Van den Berg and Labadie, 1989). However, the AQs in Cinchona are considered to be of the Rubia type.…”
Section: Introductionmentioning
confidence: 78%
“…There are two main biosynthetic pathways leading to AQs in higher plants: the polyketide pathway (Van den Berg and Labadie, 1989) and the chorismate/o-succinylbenzoic acid pathway (Leistner, 1985). In the polyketide pathway, AQs are biosynthesized from acetyl-CoA and malonyl-CoA via an octaketide chain.…”
Section: Introductionmentioning
confidence: 99%
“…It has been established that the AQs originate from a variety of different precursors and pathways [14] [15]. There are two main biosynthetic pathways leading to AQs in higher plants: the polyketide pathway [16] and the chorismate/o-succinylbenzoic acid pathway [17], the latter occurs in the Rubiaceae.…”
mentioning
confidence: 99%
“…2). HAQN pigments that are synthesized via this pathway only have one of the rings unsubstituted and at least one hydroxyl group in position R1 on the ring C. The rings A and B are derived from chorismate and -ketoglutarate via -succinylbenzoic acid (the HAQN biosynthesis branch at 1,4-dihydroxy-2-naphtoic acid), whereas ring C is formed from isopentenyl diphosphate either formed via the mevalonic acid pathway or the 2-C-methyl-D-erythritol 4-phosphate pathway 54,56,57 . The relevant colouring compounds are alizarin Figure 1.…”
Section: Natural Hydroxyanthraquinoid Pigments: Chemical Structures Omentioning
confidence: 99%
“…There are at least two biosynthetic pathways leading to HAQN pigments. On one hand, the most important is the polyketide pathway (acetate-malonate pathway) that includes suitable folding and condensation of an octaketide chain derived from acetate (acetyl-CoA) and malonate (malonyl-CoA) units 3,32,54 . The resultant polycarbonyl compounds serve as substrates for various cyclases that produce aromatic compounds that represent typical fungal metabolites.…”
Section: Natural Hydroxyanthraquinoid Pigments: Chemical Structures Omentioning
confidence: 99%