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Metabolic analysis of the cinnamate/monolignol pathway in Carthamus tinctorius seeds by a stable-isotope-dilution method
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-010-0448-0_11openalex-snapshot
Metabolomics — the link between genotypes and phenotypes
inferredcites →https://doi.org/10.1007/bf00039520openalex-snapshot
Modification of lignin biosynthesis in transgenic Nicotiana through expression of an antisense O-methyltransferase gene from Populus
inferredcites →https://doi.org/10.1007/bf00766237openalex-snapshot
Chemical structural elucidation of total lignins in woods I: fractionation of the lignin in residual wood meal after extraction of milled wood lignin
inferredcites →https://doi.org/10.1007/bf00766789openalex-snapshot
Determination of nitrobenzene oxidation products by GC and1H-NMR spectroscopy using 5-iodovanillin as a new internal standard
inferredcites →https://doi.org/10.1007/bf00771374openalex-snapshot
Lignan production inDaphne odora cell cultures
inferredcites →https://doi.org/10.1007/bf00776455openalex-snapshot
Enantiomeric compositions and biosynthesis ofWikstroemia sikokiana lignans
inferredcites →https://doi.org/10.1007/s00425-002-0865-7openalex-snapshot
Multiform biosynthetic pathway of syringyl lignin in angiosperms
inferredcites →https://doi.org/10.1007/s10086-002-0477-7openalex-snapshot
Treatment of poplar callus with ferulic and sinapic acids I: incorporation and enhancement of lignin biosynthesis
inferredcites →https://doi.org/10.1016/0031-9422(71)85029-xopenalex-snapshot
The complete structure of matairesinol monoglucoside
inferredcites →https://doi.org/10.1016/j.copbio.2005.02.007openalex-snapshot
Integrating genomics and metabolomics for engineering plant metabolic pathways
inferredcites →https://doi.org/10.1016/s0021-9258(18)99211-2openalex-snapshot
Formation of lignans (-)-secoisolariciresinol and (-)-matairesinol with Forsythia intermedia cell-free extracts
inferredcites →https://doi.org/10.1016/s0031-9422(00)85750-7openalex-snapshot
A bitter principle of safflower; matairesinol monoglucoside
inferredcites →https://doi.org/10.1016/s0031-9422(00)86527-9openalex-snapshot
A cathartic lignan glycoside isolated from Carthamus tinctorus
inferredcites →https://doi.org/10.1016/s0031-9422(00)88563-5openalex-snapshot
Tracheloside from the seeds of Carthamus tinctorius
inferredcites →https://doi.org/10.1016/s0031-9422(01)00098-xopenalex-snapshot
Repression of O-methyltransferase genes in transgenic tobacco affects lignin synthesis and plant growth
inferredcites →https://doi.org/10.1016/s0031-9422(01)00109-1openalex-snapshot
Elucidation of new structures in lignins of CAD- and COMT-deficient plants by NMR
inferredcites →https://doi.org/10.1016/s0031-9422(02)00434-xopenalex-snapshot
Structural and compositional modifications in lignin of transgenic alfalfa down-regulated in caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase
inferredcites →https://doi.org/10.1021/ja01519a036openalex-snapshot
Studies of Lignin Biosynthesis Using Isotopic Carbon. VIII. Isolation of Radioactive Hydrogenolysis Products of Lignin1
inferredcites →https://doi.org/10.1021/jf011565xopenalex-snapshot
Evidence for the Biosynthetic Pathway from Sinapic Acid to Syringyl Lignin Using Labeled Sinapic Acid with Stable Isotope at Both Methoxy Groups in Robinia pseudoacacia and Nerium indicum
inferredcites →https://doi.org/10.1021/jf047787nopenalex-snapshot
Simplified Preparation of Coniferyl and Sinapyl Alcohols
inferredcites →https://doi.org/10.1023/a:1013713905833openalex-snapshot
Metabolomics – the link between genotypes and phenotypes
inferredcites →https://doi.org/10.1023/b:phyt.0000045487.02836.32openalex-snapshot
Diversity in lignan biosynthesis
inferredcites →https://doi.org/10.1038/nbt966openalex-snapshot
Engineering plants with increased levels of the antioxidant chlorogenic acid
inferredcites →https://doi.org/10.1039/b107219fopenalex-snapshot
NMR characterization of lignins from transgenic poplars with suppressed caffeic acid O-methyltransferase activity
inferredcites →https://doi.org/10.1039/b304411dopenalex-snapshot
Biosynthesis of yatein in Anthriscus sylvestrisA part of this work was performed as a part of the R & D Project of Industrial Science and Technology Frontier Program supported by NEDO (New Energy and Industrial Technology Development Organization).
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.8040465.xopenalex-snapshot
Altered lignin composition in transgenic tobacco expressing O‐methyltransferase sequences in sense and antisense orientation
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.8060855.xopenalex-snapshot
A novel lignin in poplar trees with a reduced caffeic acid/5‐hydroxyferulic acid O‐methyltransferase activity
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01267.xopenalex-snapshot
Changes in secondary metabolism and deposition of an unusual lignin in the ref8 mutant of Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.96.16.8955openalex-snapshot
Coniferyl aldehyde 5-hydroxylation and methylation direct syringyl lignin biosynthesis in angiosperms
inferredcites →https://doi.org/10.1073/pnas.96.18.10045openalex-snapshot
New routes for lignin biosynthesis defined by biochemical characterization of recombinant ferulate 5-hydroxylase, a multifunctional cytochrome P450-dependent monooxygenase
inferredcites →https://doi.org/10.1074/jbc.275.9.6537openalex-snapshot
5-Hydroxyconiferyl Aldehyde Modulates Enzymatic Methylation for Syringyl Monolignol Formation, a New View of Monolignol Biosynthesis in Angiosperms
inferredcites →https://doi.org/10.1074/jbc.m006915200openalex-snapshot
Modifications in Lignin and Accumulation of Phenolic Glucosides in Poplar Xylem upon Down-regulation of Caffeoyl-Coenzyme A O-Methyltransferase, an Enzyme Involved in Lignin Biosynthesis
inferredcites →https://doi.org/10.1074/jbc.m104047200openalex-snapshot
CYP98A3 from Arabidopsis thaliana Is a 3′-Hydroxylase of Phenolic Esters, a Missing Link in the Phenylpropanoid Pathway
inferredcites →https://doi.org/10.1074/jbc.m511598200openalex-snapshot
Effects of Coumarate 3-Hydroxylase Down-regulation on Lignin Structure
inferredcites →https://doi.org/10.1104/pp.105.060525openalex-snapshot
KaPPA-View. A Web-Based Analysis Tool for Integration of Transcript and Metabolite Data on Plant Metabolic Pathway Maps
inferredcites →https://doi.org/10.1104/pp.117.1.101openalex-snapshot
Suppression of O-Methyltransferase Gene by Homologous Sense Transgene in Quaking Aspen Causes Red-Brown Wood Phenotypes1
inferredcites →https://doi.org/10.1104/pp.124.2.563openalex-snapshot
Essential Role of Caffeoyl Coenzyme A O -Methyltransferase in Lignin Biosynthesis in Woody Poplar Plants
inferredcites →https://doi.org/10.1105/tpc.010111openalex-snapshot
The Last Step of Syringyl Monolignol Biosynthesis in Angiosperms Is Regulated by a Novel Gene Encoding Sinapyl Alcohol Dehydrogenase
inferredcites →https://doi.org/10.1105/tpc.017509openalex-snapshot
The Arabidopsis thaliana REDUCED EPIDERMAL FLUORESCENCE1 Gene Encodes an Aldehyde Dehydrogenase Involved in Ferulic Acid and Sinapic Acid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.10.12.2033openalex-snapshot
Dual Methylation Pathways in Lignin Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.13.7.1567openalex-snapshot
The Last Step of Syringyl Monolignol Biosynthesis in Angiosperms Is Regulated by a Novel Gene Encoding Sinapyl Alcohol Dehydrogenase
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02857.xopenalex-snapshot
Multi‐site genetic modulation of monolignol biosynthesis suggests new routes for formation of syringyl lignin and wall‐bound ferulic acid in alfalfa (Medicago sativa L.)
inferredcites →https://doi.org/10.1126/science.148.3670.595openalex-snapshot
Lignin: Its Constitution and Formation from p -Hydroxycinnamyl Alcohol
inferredcites →https://doi.org/10.1139/o63-073openalex-snapshot
STUDIES OF LIGNIN BIOSYNTHESIS USING ISOTOPIC CARBON: XII. THE BIOSYNTHESIS AND METABOLISM OF SINAPIC ACID
inferredcites →https://doi.org/10.1139/v53-064openalex-snapshot
THE SYNTHESIS OF SYRINGALDEHYDE FROM VANILLIN
inferredcites →https://doi.org/10.1139/v62-334openalex-snapshot
THE SYNTHESIS OF LIGNIN MODEL SUBSTANCES: 5-HYDROXYVANILLIN AND 5-HYDROXYACETOGUAIACONE
inferredcites →https://doi.org/10.1271/bbb.58.230openalex-snapshot
Enantioselective Lignan Synthesis by Cell-free Extracts ofForsythia koreana
inferredcites →https://doi.org/10.1271/bbb.60.736openalex-snapshot
Formation of the Lignan (+)-Secoisolariciresinol by Cell-free Extracts ofArctium lappa
inferredcites →https://doi.org/10.1271/bbb.62.1468openalex-snapshot
Stereochemical Difference in Secoisolariciresinol Formation between Cell-free Extracts from Petioles and from Ripening Seeds ofArctium lappaL.
inferredcites →https://doi.org/10.1271/bbb.66.1262openalex-snapshot
Stereochemical Diversity in Lignan Biosynthesis ofArctium lappaL.
inferredcites →https://doi.org/10.1515/znb-1964-0810openalex-snapshot
Das Lignanglykosid Arctiin als chemotaxonomisches Merkmal in der Familie der Compositae
inferredcites →https://doi.org/10.3891/acta.chem.scand.33b-0105openalex-snapshot
Synthesis of Some Bromophenols Present in Red Algae.
inferredcites →https://doi.org/10.3987/r-1987-05-1169openalex-snapshot
The Syntheses of (R)-(+)-b-Vanillyl-g-butyrolactone and of Chiral Lignans Therefrom
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4760635openalex-extracted
Phytochemical Investigation on Trichilia Elegans a. Juss (Meliaceae) and its Chemotaxonomic Significance
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0015openalex-snapshot
Biosynthesis of Phenylpropanoids and Related Compounds (From APR Volume 2)
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0426openalex-snapshot
Biosynthesis of Phenylpropanoids and Related Compounds (From APR Volume 40)
inferred← citeshttps://doi.org/10.1002/9781444320503.ch4openalex-snapshot
Biosynthesis of Phenylpropanoids and Related Compounds
inferred← citeshttps://doi.org/10.1002/cssc.201601595openalex-snapshot
Syringaresinol: A Renewable and Safer Alternative to Bisphenol A for Epoxy‐Amine Resins
inferred← citeshttps://doi.org/10.1002/jlcr.3933openalex-snapshot
Synthesis of deuterium‐labeled cinnamic acids: Understanding the volatile benzenoid pathway in the flowers of the Japanese loquat Eriobotrya japonica
inferred← citeshttps://doi.org/10.1002/pca.2360openalex-snapshot
Optimum Yields of Dibenzylbutyrolactone‐type Lignans from Cynareae Fruits, During their Ripening, Germination and Enzymatic Hydrolysis Processes, Determined by On‐line Chromatographic Methods
inferred← citeshttps://doi.org/10.1007/978-3-319-20397-3_4openalex-snapshot
O-Methyltransferases Involved in Lignan Biosynthesis
inferred← citeshttps://doi.org/10.1007/s00210-024-03428-6openalex-snapshot
Chemistry, biosynthesis, and theranostics of antioxidant flavonoids and polyphenolics of genus Rhododendron: an overview
inferred← citeshttps://doi.org/10.1007/s10086-007-0892-xopenalex-snapshot
Biosynthesis of lignans and norlignans
inferred← citeshttps://doi.org/10.1007/s10086-008-0958-4openalex-snapshot
At5g54160 gene encodes Arabidopsis thaliana 5-hydroxyconiferaldehyde O-methyltransferase
inferred← citeshttps://doi.org/10.1007/s10086-009-1059-8openalex-snapshot
Profiling of phenylpropanoid monomers in developing xylem tissue of transgenic aspen (Populus tremuloides)
inferred← citeshttps://doi.org/10.1007/s10600-014-0977-xopenalex-snapshot
A New Flavanone Glucoside from the Flowers of Carthamus tinctorius and Assignment of Absolute Configuration
inferred← citeshttps://doi.org/10.1007/s10600-014-1034-5openalex-snapshot
Chemical Constituents of Metabolites Produced by the Actinomycete Acrocarpospora punica
inferred← citeshttps://doi.org/10.1007/s11101-009-9155-3openalex-snapshot
The cinnamate/monolignol pathway
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113462openalex-snapshot
Comprehensive review of two groups of flavonoids in Carthamus tinctorius L.
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127682openalex-snapshot
A new sesquineolignan and four new neolignans isolated from the leaves of Piper betle, a traditional medicinal plant in Myanmar
inferred← citeshttps://doi.org/10.1016/j.jplph.2014.09.003openalex-snapshot
Concentration of hinokinin, phenolic acids and flavonols in leaves and stems of Hydrocotyle leucocephala is differently influenced by PAR and ecologically relevant UV-B level
inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.08.013openalex-snapshot
Lignans as food constituents with estrogen and antiestrogen activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.03.008openalex-snapshot
Neolignans and phenylpropanoids from the roots of Piper taiwanense and their antiplatelet and antitubercular activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.05.015openalex-snapshot
Secondary metabolites produced by the fungus Monascus pilosus and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.052openalex-snapshot
Reactivity of sarcosine and 1,3-thiazolidine-4-carboxylic acid towards salicylaldehyde-derived alkynes and allenes
inferred← citeshttps://doi.org/10.1021/acs.jafc.5b00214openalex-snapshot
Electrophilic Aromatic Deuteration of Lignans: Mostly Reliable but Occasionally Aberrant Selectivities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00670openalex-snapshot
Acylated Lignans Isolated from Brachanthemum gobicum and Their Trypanocidal Activity
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00710openalex-snapshot
Modular Enantioselective Total Syntheses of the erythro-7,9-Dihydroxy- and 9-Hydroxy-7-Keto-8,4′-Oxyneolignans
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b01271openalex-snapshot
Isocyanate-Free Synthesis and Characterization of Renewable Poly(hydroxy)urethanes from Syringaresinol
inferred← citeshttps://doi.org/10.1021/np9004294openalex-snapshot
Flavanone and Diphenylpropane Glycosides and Glycosidic Acyl Esters from Viscum articulatum
inferred← citeshttps://doi.org/10.1038/s41598-019-47957-0openalex-snapshot
OsCAldOMT1 is a bifunctional O-methyltransferase involved in the biosynthesis of tricin-lignins in rice cell walls
inferred← citeshttps://doi.org/10.1055/s-0032-1328300openalex-snapshot
New Concepts, Experimental Approaches, and Dereplication Strategies for the Discovery of Novel Phytoestrogens from Natural Sources
inferred← citeshttps://doi.org/10.1074/jbc.m801131200openalex-snapshot
Characterization of Arabidopsis thaliana Pinoresinol Reductase, a New Type of Enzyme Involved in Lignan Biosynthesis
inferred← citeshttps://doi.org/10.1080/14786419.2022.2127708openalex-snapshot
A new alkaloid and a new benzaldehyde derivative from the twig of Zanthoxylum rhetsa (Roxb.) DC.
inferred← citeshttps://doi.org/10.1093/pcp/pcac164openalex-snapshot
TwoO-Methyltransferases from Phylogenetically Unrelated Cow Parsley (Anthriscus sylvestris) and Hinoki-Asunaro (Thujopsis dolabratavar.hondae) as a Signature of Lineage-Specific Evolution in Lignan Biosynthesis
inferred← citeshttps://doi.org/10.1093/plcell/koaa014openalex-snapshot
Seed-coat protective neolignans are produced by the dirigent protein AtDP1 and the laccase AtLAC5 in Arabidopsis
inferred← citeshttps://doi.org/10.1111/nph.20101openalex-snapshot
Systematic synthesis and identification of monolignol pathway metabolites
inferred← citeshttps://doi.org/10.1142/s0192415x16500130openalex-snapshot
Phytochemistry and Pharmacology ofCarthamus tinctoriusL.
inferred← citeshttps://doi.org/10.1186/s10086-022-02048-zopenalex-snapshot
Synthesis of highly deuterated coniferyl alcohol for silencing of NMR signals in the resulting dehydrogenative polymer
inferred← citeshttps://doi.org/10.2488/jwrs.65.1openalex-snapshot
Recent Advances in Lignan OMT Studies
inferred← citeshttps://doi.org/10.3389/fpls.2013.00325openalex-snapshot
Navigating the transcriptional roadmap regulating plant secondary cell wall deposition
inferred← citeshttps://doi.org/10.3390/molecules27113611openalex-snapshot
Biochemometry-Based Discovery of Phenylpropanoids from Azadirachta indica Fruits as Inhibitors of In Vitro Osteoclast Formation
inferred← citeshttps://doi.org/10.3390/plants9091232openalex-snapshot
Chemical Constituents of the Leaves of Campanula takesimana (Korean Bellflower) and Their Inhibitory Effects on LPS-induced PGE2 Production
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.10.0823copenalex-snapshot
Occurrence of guaiacyl/p-hydroxyphenyl lignin in Arabidopsis thaliana T87 cells
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.12.0515bopenalex-snapshot
Characterization of Jatropha curcas lignins
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.12.0618aopenalex-snapshot
Retraction: Characterization of lignocellulose of Erianthus ravennae in relation to enzymatic saccharification efficiency
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.12.1230aopenalex-snapshot
A lignan O-methyltransferase catalyzing the regioselective methylation of matairesinol in Carthamus tinctorius
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.13.0206aopenalex-snapshot
Characterization of three cinnamyl alcohol dehydrogenases from Carthamus tinctorius
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.13.0219aopenalex-snapshot
Characterization of 5-Hydroxyconiferaldehyde O-Methyltransferase in Oryza sativa
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.13.0527bopenalex-snapshot
A novel O-methyltransferase involved in the first methylation step of yatein biosynthesis from matairesinol in Anthriscus sylvestris
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.14.0722aopenalex-snapshot
Substrate-enantiomer selectivity of matairesinol O-methyltransferases
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.14.0903aopenalex-snapshot
A new O-methyltransferase for monolignol synthesis in Carthamus tinctorius
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.25.309openalex-snapshot
Tree Biotechnology of Tropical Acacia
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.27.305openalex-snapshot
Microscale alkaline nitrobenzene oxidation method for high-throughput determination of lignin aromatic components
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