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New Antifeedant C20 Terpenoids from Leucosceptrum canum

https://doi.org/10.1021/ol302787c
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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/anie.201000449openalex-snapshot
Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.030openalex-snapshot
Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants
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/ol200380vopenalex-snapshot
Defensive Sesterterpenoids with Unusual Antipodal Cyclopentenones from the Leaves of Leucosceptrum canum
inferredcites →https://doi.org/10.1038/nchembio.2007.5openalex-snapshot
The function of terpene natural products in the natural world
inferredcites →https://doi.org/10.1038/nchembio.578openalex-snapshot
Structure and mechanism of the diterpene cyclase ent-copalyl diphosphate synthase
inferredcites →https://doi.org/10.1039/b109860hopenalex-snapshot
Diversity of the biosynthesis of the isoprene units
inferredcites →https://doi.org/10.1093/jnci/83.11.757openalex-snapshot
Feasibility of a High-Flux Anticancer Drug Screen Using a Diverse Panel of Cultured Human Tumor Cell Lines
inferredcites →https://doi.org/10.1111/j.1469-185x.2006.00005.xopenalex-snapshot
Coloured nectar: distribution, ecology, and evolution of an enigmatic floral trait

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.201208687openalex-snapshot
Asymmetric Total Synthesis of Leucosceptroid B
inferred← citeshttps://doi.org/10.1002/ange.201407788openalex-snapshot
A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)‐Norleucosceptroid A, (−)‐Norleucosceptroid B, and (−)‐Leucosceptroid K
inferred← citeshttps://doi.org/10.1002/ange.201410134openalex-snapshot
Total Synthesis of Leucosceptroids A and B
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.201208687openalex-snapshot
Asymmetric Total Synthesis of Leucosceptroid B
inferred← citeshttps://doi.org/10.1002/anie.201407788openalex-snapshot
A General Entry to Antifeedant Sesterterpenoids: Total Synthesis of (+)‐Norleucosceptroid A, (−)‐Norleucosceptroid B, and (−)‐Leucosceptroid K
inferred← citeshttps://doi.org/10.1002/anie.201410134openalex-snapshot
Total Synthesis of Leucosceptroids A and B
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/cbdv.71143openalex-snapshot
Ent ‐Labdane Diterpenoids from the Medicinal Plant Leucosceptrum canum
inferred← citeshttps://doi.org/10.1002/chem.201603061openalex-snapshot
A Divergent Approach to the Marine Diterpenoids (+)‐Dictyoxetane and (+)‐Dolabellane V
inferred← citeshttps://doi.org/10.1002/ffj.70017openalex-snapshot
Leucosceptrum canum Sm. Essential Oil: A Natural Solution for Sustainable Nematode and Bacterial Management
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/10.1007/978-981-99-7329-3_4openalex-snapshot
Diverse Novel Sesterterpenoids
inferred← citeshttps://doi.org/10.1007/s11426-016-0076-6openalex-snapshot
Recent advances in terpenoid syntheses from China
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.fitote.2026.107328openalex-snapshot
Chemical diversity of abietane diterpenoids from Nepeta stewartiana Diels and their anti-bacterial and antifeedant effects
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.01.009openalex-snapshot
Isolation of an acidic polysaccharide from the flowers of Leucosceptrum canum Smith and its immunomodulatory activity evaluation
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106294openalex-snapshot
Bioactive flavonoids from Leucosceptrum canum with nematicidal efficacy and mechanistic insights through acetylcholinesterase inhibition and docking study
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.2024.114305openalex-snapshot
Immunosuppressive leucosceptrane-type sesterterpenoids with antipodal cyclopentenones isolated from Leucosceptrum canum
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/j.tetlet.2021.153356openalex-snapshot
Leucoabietenes A and B, rearranged abietane and ent-abietane diterpene hydrocarbons against resistant infectious fungus and bacterium from the leaves of Leucosceptrum canum
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.joc.6c00172openalex-snapshot
Exploring Diversified Abietane Diterpenoids from Leucosceptrum canum with Immunosuppressive and Antifungal Activities
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.1c00369openalex-snapshot
Immunosuppressive and Adipogenesis Inhibitory Sesterterpenoids with a Macrocyclic Ether System from Eurysolen gracilis
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/10.1021/ol4004756openalex-snapshot
Peltate Glandular Trichomes of Colquhounia coccinea var. mollis Harbor a New Class of Defensive Sesterterpenoids
inferred← citeshttps://doi.org/10.1021/ol503230sopenalex-snapshot
Unraveling the Metabolic Pathway in Leucosceptrum canum by Isolation of New Defensive Leucosceptroid Degradation Products and Biomimetic Model Synthesis
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/d1np00021gopenalex-snapshot
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/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/10.1101/2024.12.20.629783openalex-snapshot
Rule-Based Deconstruction and Reconstruction of Diterpene Libraries: Categorizing Patterns & Unravelling the Structural Landscape
inferred← citeshttps://doi.org/10.1111/nph.15778openalex-snapshot
Promiscuous terpene synthases from Prunella vulgaris highlight the importance of substrate and compartment switching in terpene synthase evolution
inferred← citeshttps://doi.org/10.3389/fpls.2026.1833733openalex-snapshot
Integrated characterization of six sesquiterpene synthases unravels diversified terpene biosynthesis in the mint species Leucosceptrum canum
inferred← citeshttps://doi.org/10.3390/molecules23010057openalex-snapshot
Cytotoxic Terpenoids from the Roots of Dracocephalum taliense
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