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Unraveling the Metabolic Pathway in Leucosceptrum canum by Isolation of New Defensive Leucosceptroid Degradation Products and Biomimetic Model Synthesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Recent Advances in Aldolase‐Catalyzed Asymmetric Synthesis
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Biomimetic Total Synthesis of Litseaverticillols A, C, D, F, and G: Singlet‐Oxygen‐Initiated Cascades
inferredcites →https://doi.org/10.1002/anie.201000449openalex-snapshot
Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids
inferredcites →https://doi.org/10.1002/anie.201208687openalex-snapshot
Asymmetric Total Synthesis of Leucosceptroid B
inferredcites →https://doi.org/10.1002/anie.201407477openalex-snapshot
One‐Pot Transformation of Simple Furans into 4‐Hydroxy‐2‐cyclopentenones in Water
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A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)‐Norleucosceptroid A, (−)‐Norleucosceptroid B, and (−)‐Leucosceptroid K
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Total Synthesis of Leucosceptroids A and B
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Kumulierte Ylide, XII. Eine stereoselektive Synthesemethode für (Z)‐α,β‐ungesättigte Aldehyde2)
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Maoecrystal V, Cytotoxic Diterpenoid with a Novel C19 Skeleton from Isodon eriocalyx (Dunn.) Hara.
inferredcites →https://doi.org/10.1007/s00425-010-1156-3openalex-snapshot
Apocarotenoids: hormones, mycorrhizal metabolites and aroma volatiles
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Directed evolution of aldolases for exploitation in synthetic organic chemistry
inferredcites →https://doi.org/10.1016/j.phytochem.2012.11.008openalex-snapshot
Defense sesterterpenoid lactones from Leucosceptrum canum
inferredcites →https://doi.org/10.1016/j.tet.2006.01.110openalex-snapshot
The power of singlet oxygen chemistry in biomimetic syntheses
inferredcites →https://doi.org/10.1016/j.tetlet.2012.11.010openalex-snapshot
Unusual antifeedant spiro-sesterterpenoid from the flowers of Leucosceptrum canum
inferredcites →https://doi.org/10.1016/s0040-4020(01)96576-7openalex-snapshot
Singlet oxygen photooxygenation of furans
inferredcites →https://doi.org/10.1021/ar800023vopenalex-snapshot
Using Singlet Oxygen to Synthesize Polyoxygenated Natural Products from Furans
inferredcites →https://doi.org/10.1021/cr9004023openalex-snapshot
Meliaceous Limonoids: Chemistry and Biological Activities
inferredcites →https://doi.org/10.1021/ja01146a542openalex-snapshot
THE BASE CATALYZED DECOMPOSITION OF A DIALKYL PEROXIDE
inferredcites →https://doi.org/10.1021/jo00368a025openalex-snapshot
Metabolites of the nudibranch Chromodoris funerea and the singlet oxygen oxidation products of furodysin and furodysinin
inferredcites →https://doi.org/10.1021/jo030337uopenalex-snapshot
LeucosceptrineA Novel Sesterterpene with Prolylendopeptidase Inhibitory Activity from Leucosceptrum canum
inferredcites →https://doi.org/10.1021/jo200899vopenalex-snapshot
Asymmetric Synthesis of the Core Structure of Leucosceptroids A–D
inferredcites →https://doi.org/10.1021/ol040040yopenalex-snapshot
Novel Sesterterpenes from Leucosceptrum canum of Nepalese Origin
inferredcites →https://doi.org/10.1021/ol0481535openalex-snapshot
Maoecrystal V, Cytotoxic Diterpenoid with a Novel C19 Skeleton from Isodon eriocalyx (Dunn.) Hara
inferredcites →https://doi.org/10.1021/ol200380vopenalex-snapshot
Defensive Sesterterpenoids with Unusual Antipodal Cyclopentenones from the Leaves of Leucosceptrum canum
inferredcites →https://doi.org/10.1021/ol3013205openalex-snapshot
Ternifolide A, a New Diterpenoid Possessing a Rare Macrolide Motif from Isodon ternifolius
inferredcites →https://doi.org/10.1021/ol3017879openalex-snapshot
Unique Proline–Benzoquinone Pigment from the Colored Nectar of “Bird’s Coca Cola Tree” Functions in Bird Attractions
inferredcites →https://doi.org/10.1021/ol302787copenalex-snapshot
New Antifeedant C20 Terpenoids from Leucosceptrum canum
inferredcites →https://doi.org/10.1021/ol4004756openalex-snapshot
Peltate Glandular Trichomes of Colquhounia coccinea var. mollis Harbor a New Class of Defensive Sesterterpenoids
inferredcites →https://doi.org/10.1023/a:1022523329255openalex-snapshot
Photooxidation of Nimbin and Salannin, Tetranortriterpenoids from the Neem Tree (Azadirachta indica)
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The function of terpene natural products in the natural world
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Triterpenoids from the Schisandraceae family
inferredcites →https://doi.org/10.1104/pp.102.017921openalex-snapshot
Elucidation of the Indirect Pathway of Abscisic Acid Biosynthesis by Mutants, Genes, and Enzymes
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The Strigolactone Germination Stimulants of the Plant-Parasitic Striga and Orobanche spp. Are Derived from the Carotenoid Pathway
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Identification and Regulation of TPS04/GES, an Arabidopsis Geranyllinalool Synthase Catalyzing the First Step in the Formation of the Insect-Induced Volatile C16-Homoterpene TMTT
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The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles β‐ionone, pseudoionone, and geranylacetone
inferredcites →https://doi.org/10.1111/j.1742-4658.2008.06820.xopenalex-snapshot
Characterization of the rice carotenoid cleavage dioxygenase 1 reveals a novel route for geranial biosynthesis
inferredcites →https://doi.org/10.1126/science.1116232openalex-snapshot
Genetic Engineering of Terpenoid Metabolism Attracts Bodyguards to Arabidopsis
inferredcites →https://doi.org/10.3390/70200112openalex-snapshot
Photooxygenation of Nimonol, a Tetranortriterpenoid from Azadirachta indica. A. Juss.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112780zenodo-depositor-declared
Immunosuppressive gentianellane-type sesterterpenoids from the traditional Uighur medicine Gentianella turkestanorum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113531zenodo-depositor-declared
Labdane diterpenoids from the heartwood of Leucosceptrum canum that impact on root growth and seed germination of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1002/ange.202421497openalex-snapshot
Discovery and Total Synthesis of a New Class of Minor Immunosuppressive Plant Sesterterpenoids
inferred← citeshttps://doi.org/10.1002/anie.202421497openalex-snapshot
Discovery and Total Synthesis of a New Class of Minor Immunosuppressive Plant Sesterterpenoids
inferred← citeshttps://doi.org/10.1002/rcm.7632openalex-snapshot
Analysis of the lithiated leucosceptroids from Leucosceptrum canum to facilitate their identification and differentiation by electrospray ionization tandem mass spectrometry
inferred← citeshttps://doi.org/10.1002/slct.202500108openalex-snapshot
Phytochemical Profiling and Bioactivity of Leucosceptrum Canum Extracts from the Uttarakhand Himalayas: Nematicidal and Acetylcholinesterase Inhibitory Potential
inferred← citeshttps://doi.org/10.1007/s13659-016-0094-6openalex-snapshot
Drimane Sesquiterpenoids and Isochromone Derivative from the Endophytic Fungus Pestalotiopsis sp. M-23
inferred← citeshttps://doi.org/10.1016/j.bmc.2018.12.023openalex-snapshot
Leucoflavonine, a new bioactive racemic flavoalkaloid from the leaves of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.bse.2024.104849openalex-snapshot
Leucosceptrum canum sm.: A comprehensive review on phytochemistry, biological applications and chemophenetic values
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.07.004openalex-snapshot
Total synthesis of norleucosceptroids F and G
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.10.010openalex-snapshot
Diversified abietane family diterpenoids from the leaves of Leucosceptrum canum and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112325openalex-snapshot
Unusual glycosidic labdane diterpenoids with cytotoxicity from the root of Phlomoides betonicoides
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114185openalex-snapshot
Immunosuppressive leucosesterterpane and penta-nor-leucosesterterpane sesterterpenoids from Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114706openalex-snapshot
γ-lactam and γ-lactone-containing sesterterpenoids from Colquhounia coccinea var. mollis with immunosuppressive activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114844openalex-snapshot
Nine previously undescribed immunosuppressive ent-labdane diterpenoids from the roots of Eurysolen gracilis
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30109-8openalex-snapshot
Leucosceptroid B from glandular trichomes of Leucosceptrum canum reduces fat accumulation in Caenorhabditis elegans through suppressing unsaturated fatty acid biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c01759openalex-snapshot
Leucosceptrane Sesterterpenoids as a New Type of Natural Immunosuppressive Agents in Treating Sepsis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00553openalex-snapshot
Discovery of Unusual Sesterterpenoids from Colquhounia coccinea var. mollis and Their Metabolic Implications
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02597openalex-snapshot
Synthetic Studies toward Leucosceptroid Family of Natural Products
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00374openalex-snapshot
Immunosuppresive Sesterterpenoids and Norsesterterpenoids from Colquhounia coccinea var. mollis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02796openalex-snapshot
Syntheses of Linear Biosynthetic C25-Precursors of Leucosceptroids
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02459openalex-snapshot
Spectroscopic and Computational Strategy for the Absolute Configuration Determination of Immunosuppressive Spiroketal and Cyclopentanone-Containing Sesterterpenoids from Colquhounia coccinea var. mollis
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01672openalex-snapshot
Stereoselective Construction of the Highly Congested Tricyclic Core Structure in Leucosceptroid H
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04812openalex-snapshot
Macrocyclic Decanor- (C15) and Pentanor- (C20) Sesterterpenoids and C25 Precursor with Immunosuppressive Activity from Leucosceptrum canum
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04044openalex-snapshot
Detoxification of Plant Aromatic Abietanoids via Cleavage of the Benzene Ring into 11,12-Seco-diterpene Polyenes by a Specialist Insect of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1021/jacs.5b02021openalex-snapshot
Total Synthesis of the Leucosceptroid Family of Natural Products
inferred← citeshttps://doi.org/10.1039/c5cc00879dopenalex-snapshot
Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone
inferred← citeshttps://doi.org/10.1039/c6ob02488bopenalex-snapshot
Bioinspired total syntheses of terpenoids
inferred← citeshttps://doi.org/10.1039/c8np00050fopenalex-snapshot
Total synthesis of sesterterpenoids
inferred← citeshttps://doi.org/10.1039/d0np00070aopenalex-snapshot
Sesterterpenoids: chemistry, biology, and biosynthesis
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The untapped potential of plant sesterterpenoids: chemistry, biological activities and biosynthesis
inferred← citeshttps://doi.org/10.1039/d2qo00138aopenalex-snapshot
A monocarbocyclic sesterterpenoid biosynthetic precursor of leucosceptroids from Leucosceptrum canum and its metabolic isomerization by a specialist insect
inferred← citeshttps://doi.org/10.1039/d3np00058copenalex-snapshot
The Kornblum DeLaMare rearrangement in natural product synthesis: 25 years of innovation
inferred← citeshttps://doi.org/10.1039/d4cc03674copenalex-snapshot
Selenium dioxide promoted selenylation/cyclization of leucosceptrane sesterterpenoids
inferred← citeshttps://doi.org/10.1039/d4np00041bopenalex-snapshot
Sesterterpenoids: sources, structural diversity, biological activity, and data management
inferred← citeshttps://doi.org/10.1039/d4ob00334aopenalex-snapshot
Unusual immunosuppressive pyridine-containing bisnor - (c 23 ), tetranor - (c 21 ) and pentanor - (c 20 ) sesterterpenoids from Tibetan Leucosceptrum canum
inferred← citeshttps://doi.org/10.1105/tpc.15.00715openalex-snapshot
A Geranylfarnesyl Diphosphate Synthase Provides the Precursor for Sesterterpenoid (C25) Formation in the Glandular Trichomes of the Mint Species Leucosceptrum canum
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Biomimetic Synthesis of Biologically Active Natural Products: An Updated Review
inferred← citeshttps://doi.org/10.3390/molecules23010057openalex-snapshot
Cytotoxic Terpenoids from the Roots of Dracocephalum taliense
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