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Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids

https://doi.org/10.1002/anie.201000449
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4899-5355-1_8openalex-snapshot
The Chemistry of Biologically Active Constituents Secreted and Stored in Plant Glandular Trichomes
inferredcites →https://doi.org/10.1007/s00425-006-0376-zopenalex-snapshot
Microchemical analysis of laser-microdissected stone cells of Norway spruce by cryogenic nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1016/0014-5793(94)80475-3openalex-snapshot
A novel prenyltransferase, farnesylgeranyl diphosphate synthase, from the haloalkaliphilic archaeon, Natronobacterium pharaonis
inferredcites →https://doi.org/10.1021/jo030337uopenalex-snapshot
LeucosceptrineA Novel Sesterterpene with Prolylendopeptidase Inhibitory Activity from Leucosceptrum canum
inferredcites →https://doi.org/10.1021/ol040040yopenalex-snapshot
Novel Sesterterpenes from Leucosceptrum canum of Nepalese Origin
inferredcites →https://doi.org/10.1038/5202openalex-snapshot
Strategies for bioengineering the development and metabolism of glandular tissues in plants
inferredcites →https://doi.org/10.1038/86770openalex-snapshot
Suppression of a P450 hydroxylase gene in plant trichome glands enhances natural-product-based aphid resistance
inferredcites →https://doi.org/10.1038/nchembio.2007.5openalex-snapshot
The function of terpene natural products in the natural world
inferredcites →https://doi.org/10.1039/b617259hopenalex-snapshot
Sesterterpenoids
inferredcites →https://doi.org/10.1046/j.1432-1327.2000.00967.xopenalex-snapshot
Novel prenyltransferase gene encoding farnesylgeranyl diphosphate synthase from a hyperthermophilic archaeon, Aeropyrum pernix
inferredcites →https://doi.org/10.1093/aob/mch011openalex-snapshot
New Approaches for Studying and Exploiting an Old Protuberance, the Plant Trichome
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.

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Labdane diterpenoids from the heartwood of Leucosceptrum canum that impact on root growth and seed germination of Arabidopsis thaliana
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Harnessing Plant Trichome Biochemistry for the Production of Useful Compounds
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Chirality
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From Monocyclization to Pentacyclization: A Versatile Plant Cyclase Produces Diverse Sesterterpenes with Anti‐Liver Fibrosis Potential
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Asymmetric Total Synthesis of Leucosceptroid B
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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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A Cryptic Plant Terpene Cyclase Producing Unconventional 18‐ and 14‐Membered Macrocyclic C25 and C20 Terpenoids with Immunosuppressive Activity
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Discovery and Total Synthesis of a New Class of Minor Immunosuppressive Plant Sesterterpenoids
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Asymmetric Cyclopropanation of Alkenes with Dimethyl Diazomalonate Catalyzed by Chiral Diene–Rhodium Complexes
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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.202110842openalex-snapshot
A Cryptic Plant Terpene Cyclase Producing Unconventional 18‐ and 14‐Membered Macrocyclic C25 and C20 Terpenoids with Immunosuppressive Activity
inferred← citeshttps://doi.org/10.1002/anie.202421497openalex-snapshot
Discovery and Total Synthesis of a New Class of Minor Immunosuppressive Plant Sesterterpenoids
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New Bioactive Macrocyclic Diterpenoids from Euphorbia helioscopia
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Ent ‐Labdane Diterpenoids from the Medicinal Plant Leucosceptrum canum
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A Divergent Approach to the Marine Diterpenoids (+)‐Dictyoxetane and (+)‐Dolabellane V
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ChemInform Abstract: Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids.
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Defensive Sesquiterpenoids from Leaves of Eupatorium adenophorum
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Stereoselective Strategies for the Synthesis of Functionalized Cis ‐Hydrindanes in Natural Product Synthesis
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Localisation of Two Bioactive Labdane Diterpenoids in the Peltate Glandular Trichomes of Leonurus japonicus by Laser Microdissection Coupled with UPLC‐MS/MS
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Discovery of diversified cassane diterpenoids as potent antibacterial agents from Caesaplinia pulcherrima and their mechanisms
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/s10886-026-01749-9openalex-snapshot
Microbes Isolated from Ailanthus altissima Leaves Contribute to Samia cynthia’s Tolerance to the Toxic Quassinoid Diterpenoid
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Recent advances in terpenoid syntheses from China
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Developmental Ultrastructure of Glandular Trichomes of Rosmarinus officinalis: Secretory Cavity and Secretory Vesicle Formation
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
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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.cclet.2015.07.004openalex-snapshot
Total synthesis of norleucosceptroids F and G
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.04.067openalex-snapshot
Characterization of two chimeric sesterterpene synthases from a fungal symbiont isolated from a sesterterpenoid-producing Lamiaceae plant Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105379openalex-snapshot
Chemical investigation of Buddleja officinalis leaves and localization of defensive triterpenoids to its glandular trichomes
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106158openalex-snapshot
Leucosceptrane sesterterpenoids from Tibetan Leucosceptrum canum and their immunosuppressive activity
inferred← citeshttps://doi.org/10.1016/j.foodres.2022.112323openalex-snapshot
Morphology and mass spectrometry-based chemical profiling of peltate glandular trichomes on Mentha haplocalyx Briq leaves
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.indcrop.2019.03.039openalex-snapshot
Wormwood (Artemisia absinthium L.) as a promising nematicidal and antifungal agent: Chemical composition, comparison of extraction techniques and bioassay-guided isolation
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122020openalex-snapshot
Novel β-macrocarpene sesquiterpenoids from maize with inhibition potential against Spodoptera pests via species-specific mechanisms
inferred← citeshttps://doi.org/10.1016/j.molp.2015.10.010openalex-snapshot
Structural Analyses of Short-Chain Prenyltransferases Identify an Evolutionarily Conserved GFPPS Clade in Brassicaceae Plants
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.2016.12.021openalex-snapshot
Chemical profile and defensive function of the latex of Euphorbia peplus
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.2019.03.009openalex-snapshot
Characterization of a sesquiterpene cyclase from the glandular trichomes of Leucosceptrum canum for sole production of cedrol in Escherichia coli and Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112285openalex-snapshot
Peltate glandular trichomes of Colquhounia vestita harbor diterpenoid acids that contribute to plant adaptation to UV radiation and cold stresses
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.2021.112731openalex-snapshot
Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112780openalex-snapshot
Immunosuppressive gentianellane-type sesterterpenoids from the traditional Uighur medicine Gentianella turkestanorum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113852openalex-snapshot
Defensive furofuran lignans localized to the oil cells of Neocinnamomum delavayi and their metabolism by a specialist insect
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.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.pld.2017.05.004openalex-snapshot
Localization of a defensive volatile 4-hydroxy-4-methylpentan-2-one in the capitate glandular trichomes of Oenothera glazioviana
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.005openalex-snapshot
Grob-type fragmentation of 5-oxabicyclo[2.1.1]hexane system: a strategy for synthesis of annulated and 2,2,5-trisubstituted tetrahydrofurans
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.2016.11.007openalex-snapshot
Recent application of oxa-Michael reaction in complex natural product synthesis
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/j.tetlet.2025.155554openalex-snapshot
New labdane diterpenoid glycosides from the leaves and flowers of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.155972openalex-snapshot
Gentianellin A, an unusual immunosuppressive sesterterpenoid from the traditional Tibetan medicine Gentianella azurea
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100051openalex-snapshot
Molecular Basis for Sesterterpene Diversity Produced by Plant Terpene Synthases
inferred← citeshttps://doi.org/10.1016/j.xplc.2021.100184openalex-snapshot
Occurrence and biosynthesis of plant sesterterpenes (C25), a new addition to terpene diversity
inferred← citeshttps://doi.org/10.1016/j.xplc.2021.100233openalex-snapshot
An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids
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.accounts.0c00727openalex-snapshot
In Pursuit of Synthetic Efficiency: Convergent Approaches
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00834openalex-snapshot
Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c00853openalex-snapshot
Cassane Diterpenoids from the Aerial Parts of Caesalpinia pulcherrima and Their Antifeedant and Insecticidal Activities against Mythimna separate and Plutella xylostella
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c04218openalex-snapshot
Negative Interactions Balance Growth and Defense in Plants Confronted with Herbivores or Pathogens
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c02779openalex-snapshot
Caterpillars Detoxify Diterpenoid from Nepeta stewartiana by the Molting Hormone Gene CYP306A1
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.0c00272openalex-snapshot
Gentianelloids A and B: Immunosuppressive 10,11-seco-Gentianellane Sesterterpenoids from the Traditional Uighur Medicine Gentianella turkestanorum
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.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.5c05377openalex-snapshot
Enantioselective Synthesis of Bicyclo[4.3.0]nonatrienones via Palladium-Catalyzed Desymmetric 1,5-Enyne Cycloisomerization
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/jf401921xopenalex-snapshot
Neopierisoids A and B, Two New Chlorinated 3,4-seco-Grayanane Diterpenoids with Antifeedant Activity from Flowers of Pieris japonica
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/np400971ropenalex-snapshot
Biologically Active Dichapetalins from Dichapetalum gelonioides
inferred← citeshttps://doi.org/10.1021/ol200380vopenalex-snapshot
Defensive Sesterterpenoids with Unusual Antipodal Cyclopentenones from the Leaves of Leucosceptrum canum
inferred← citeshttps://doi.org/10.1021/ol300099eopenalex-snapshot
Schilancitrilactones A–C: Three Unique Nortriterpenoids from Schisandra lancifolia
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/ol3017879openalex-snapshot
Unique Proline–Benzoquinone Pigment from the Colored Nectar of “Bird’s Coca Cola Tree” Functions in Bird Attractions
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/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/10.1038/s41467-025-63055-4openalex-snapshot
Noncanonical terpene cyclases for the biosynthesis of diterpenoids regulating chlamydospore formation in plant-associated Trichoderma
inferred← citeshttps://doi.org/10.1039/c2np20005hopenalex-snapshot
Synthetic approaches toward sesterterpenoids
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/c8np00077hopenalex-snapshot
Non-volatile natural products in plant glandular trichomes: chemistry, biological activities and biosynthesis
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/10.1039/d6np00005copenalex-snapshot
Syntheses of furan natural products
inferred← citeshttps://doi.org/10.1039/d6np00035eopenalex-snapshot
Growth, signals, and survival: the evolutionary divergence of terpenoid metabolism in terrestrial plants
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/10.1093/treephys/tpy115openalex-snapshot
Storage of defense metabolites in the leaves of Myrtaceae: news of the eggs in different baskets
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/10.1111/jipb.12242openalex-snapshot
Peltate glandular trichomes ofColquhounia seguiniiharbor new defensive clerodane diterpenoids
inferred← citeshttps://doi.org/10.1111/tpj.13064openalex-snapshot
Arabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate geranylfarnesyl diphosphate
inferred← citeshttps://doi.org/10.1126/sciadv.adw2578openalex-snapshot
Plant defense-directed discovery of a natural anti-psoriasis agent targeting GAPDH
inferred← citeshttps://doi.org/10.1360/n052015-00073openalex-snapshot
Specialized Metabolism in Plant Glandular Trichomes
inferred← citeshttps://doi.org/10.18174/543999openalex-snapshot
Mapping natural product diversity through genomics
inferred← citeshttps://doi.org/10.2174/1389557523666230417083143openalex-snapshot
Biomimetic Synthesis of Biologically Active Natural Products: An Updated Review
inferred← citeshttps://doi.org/10.32615/bp.2022.027openalex-snapshot
Glandular trichomes of medicinal plants: types, separation and purification, biological activities
inferred← citeshttps://doi.org/10.3389/fpls.2019.01166openalex-snapshot
Terpene Synthases as Metabolic Gatekeepers in the Evolution of Plant Terpenoid Chemical Diversity
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/foods13182993openalex-snapshot
Qualitative Profiling, Antioxidant and Antimicrobial Activities of Polar and Nonpolar Basil Extracts
inferred← citeshttps://doi.org/10.3390/ijms222413262openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/insects16020136openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules22091431openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules23010057openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ph15111392openalex-snapshot
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inferred← citeshttps://doi.org/10.7717/peerj.17866openalex-snapshot
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