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Defensive Sesterterpenoids with Unusual Antipodal Cyclopentenones from the Leaves of Leucosceptrum canum

https://doi.org/10.1021/ol200380v
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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/10.1016/0031-9422(88)80440-0openalex-snapshot
Further sesterterpenes from Salvia hypoleuca
inferredcites →https://doi.org/10.1016/s0021-9258(19)81477-1openalex-snapshot
Biosynthesis of monoterpenes. Enantioselectivity in the enzymatic cyclization of (+)- and (-)-linalyl pyrophosphate to (+)- and (-)-pinene and (+)- and (-)-camphene.
inferredcites →https://doi.org/10.1016/s0040-4020(02)01491-6openalex-snapshot
Natural anti-HIV agents. Part 3: Litseaverticillols A–H, novel sesquiterpenes from Litsea verticillata
inferredcites →https://doi.org/10.1021/cr050286wopenalex-snapshot
Structural Biology and Chemistry of the Terpenoid Cyclases
inferredcites →https://doi.org/10.1021/ol040040yopenalex-snapshot
Novel Sesterterpenes from Leucosceptrum canum of Nepalese Origin
inferredcites →https://doi.org/10.1038/nchembio.2007.5openalex-snapshot
The function of terpene natural products in the natural world
inferredcites →https://doi.org/10.1111/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/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/10.1007/978-3-031-59567-7_2openalex-snapshot
The Chemical Ecology of Plant Natural Products
inferred← citeshttps://doi.org/10.1007/s11426-016-0076-6openalex-snapshot
Recent advances in terpenoid syntheses from China
inferred← citeshttps://doi.org/10.1007/s13659-014-0009-3openalex-snapshot
Antifeedant and Antiviral Diterpenoids from the Fresh Roots of Euphorbia jolkinii
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/b978-0-08-096805-6.00007-3openalex-snapshot
Five-Membered Ring Systems: Furans and Benzofurans
inferred← citeshttps://doi.org/10.1016/b978-0-08-096807-0.00007-5openalex-snapshot
Five-Membered Ring Systems: Furans and Benzofurans
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14668-2openalex-snapshot
Sesterterpene Biosynthesis: Cyclization Mechanisms and Oxidative Modifications
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.2012.11.008openalex-snapshot
Defense sesterterpenoid lactones from Leucosceptrum canum
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.2012.11.010openalex-snapshot
Unusual antifeedant spiro-sesterterpenoid from the flowers of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155554openalex-snapshot
New labdane diterpenoid glycosides from the leaves and flowers of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/s1875-5364(13)60036-9openalex-snapshot
Natural products chemistry research: progress in China in 2011
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/10.1016/s1875-5364(24)60657-6openalex-snapshot
Glasesterterpenoids A−C: three sesterterpenoids with 7-cyclohexyldecahydronaphthalene carbon skeleton isolated from the root of Lindera glauca
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.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.2c01364openalex-snapshot
Linderasesterterpenoids A and B: Two 7-Cyclohexyldecahydroazulene Carbon Skeleton Sesterterpenoids Isolated from the Root of Lindera glauca
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00586openalex-snapshot
(+)-Thalianatriene and (−)-Retigeranin B Catalyzed by Sesterterpene Synthases from Arabidopsis thaliana
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/jo200899vopenalex-snapshot
Asymmetric Synthesis of the Core Structure of Leucosceptroids A–D
inferred← citeshttps://doi.org/10.1021/np400678hopenalex-snapshot
Limonoids from Aphanamixis polystachya and Their Antifeedant Activity
inferred← citeshttps://doi.org/10.1021/ol3008149openalex-snapshot
Aphanamixoid A, a Potent Defensive Limonoid, with a New Carbon Skeleton from Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1021/ol302787copenalex-snapshot
New Antifeedant C20 Terpenoids from Leucosceptrum canum
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/ol401005jopenalex-snapshot
Asperterpenols A and B, New Sesterterpenoids Isolated from a Mangrove Endophytic Fungus Aspergillus sp. 085242
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/c2np20005hopenalex-snapshot
Synthetic approaches toward sesterterpenoids
inferred← citeshttps://doi.org/10.1039/c3cc37571dopenalex-snapshot
Regio- and stereoselective synthesis of 2-cyclopentenones via a hydrogenolysis-terminated Heck cyclization of β-alkylthio dienones
inferred← citeshttps://doi.org/10.1039/c3np20089bopenalex-snapshot
Sesterterpenoids
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/10.1073/pnas.1705567114openalex-snapshot
Unearthing a sesterterpene biosynthetic repertoire in the Brassicaceae through genome mining reveals convergent evolution
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
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2011.03894.xopenalex-snapshot
Dark purple nectar as a foraging signal in a bird‐pollinated Himalayan plant
inferred← citeshttps://doi.org/10.2174/1389557523666230417083143openalex-snapshot
Biomimetic Synthesis of Biologically Active Natural Products: An Updated Review
inferred← citeshttps://doi.org/10.3389/fcell.2023.1125723openalex-snapshot
Updated perspective of EPAS1 and the role in pulmonary hypertension
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/10.3762/bjoc.12.200openalex-snapshot
The direct oxidative diene cyclization and related reactions in natural product synthesis
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