On the public citation graph
CYP712K4 Catalyzes the C-29 Oxidation of Friedelin in the Maytenus ilicifolia Quinone Methide Triterpenoid Biosynthesis Pathway
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1 of the 51 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1046/j.1365-313x.2003.01676.x (notice 2015-11-13).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/pca.626openalex-snapshotQuantitative determination of cytotoxicFriedo‐nor‐oleanane derivatives from five morphological types of Maytenus ilicifolia (celastraceae) by reverse‐phase high‐performance liquid chromatography
inferredcites →https://doi.org/10.1002/yea.1502openalex-snapshotA suite of Gateway® cloning vectors for high‐throughput genetic analysis in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.phrs.2017.11.027openalex-snapshotA promising natural product, pristimerin, results in cytotoxicity against breast cancer stem cells in vitro and xenografts in vivo through apoptosis and an incomplete autopaghy in breast cancer
inferredcites →https://doi.org/10.1038/ncomms14153openalex-snapshotThe ancient CYP716 family is a major contributor to the diversification of eudicot triterpenoid biosynthesis
inferredcites →https://doi.org/10.1038/srep22627openalex-snapshotMevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging
inferredcites →https://doi.org/10.1038/srep36858openalex-snapshotFriedelin Synthase from Maytenus ilicifolia: Leucine 482 Plays an Essential Role in the Production of the Most Rearranged Pentacyclic Triterpene
inferredcites →https://doi.org/10.1073/pnas.1323369111openalex-snapshotCombinatorial biosynthesis of sapogenins and saponins in Saccharomyces cerevisiae using a C-16α hydroxylase from Bupleurum falcatum
inferredcites →https://doi.org/10.1111/nph.12325openalex-snapshotBioengineering of plant (tri)terpenoids: from metabolic engineering of plants to synthetic biology in vivo and in vitro
inferredcites →https://doi.org/10.1111/nph.15809openalex-snapshotFriedelane‐type triterpene cyclase in celastrol biosynthesis from Tripterygium wilfordii and its application for triterpenes biosynthesis in yeast
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/med.21751openalex-snapshotBiosynthesis, total synthesis, structural modifications, bioactivity, and mechanism of action of the quinone‐methide triterpenoid celastrol
inferred← citeshttps://doi.org/10.1007/s00299-021-02748-8openalex-snapshotDe novo transcriptome analysis and identification of candidate genes associated with triterpenoid biosynthesis in Trichosanthes cucumerina L.
inferred← citeshttps://doi.org/10.1111/nph.18272openalex-snapshotThe tomato cytochrome P450 CYP712G1 catalyses the double oxidation of orobanchol en route to the rhizosphere signalling strigolactone, solanacol
inferred← citeshttps://doi.org/10.17504/protocols.io.bspfndjnopenalex-snapshotProtocols for "The genome analysis of Tripterygium wilfordii reveals TwCYP712K1 and TwCYP712K2 responsible for oxidation of friedelin in celastrol biosynthesis pathway" v1
inferred← citeshttps://doi.org/10.3390/molecules26226806openalex-snapshotThe Methionine 549 and Leucine 552 Residues of Friedelin Synthase from Maytenus ilicifolia Are Important for Substrate Binding Specificity
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