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Enantiomeric Lignans and Neolignans from Phyllanthus glaucus: Enantioseparation and Their Absolute Configurations

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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/cbdv.201000110openalex-snapshot

Two New Lignans and Anti‐HBV Constituents from Illicium henryi

inferredcites →https://doi.org/10.1002/cbdv.201200244openalex-snapshot

Chemical Constituents of the Plants from the Genus Phyllanthus

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Chiroptical properties of 2,3‐dihydrobenzo[b]furan and chromane chromophores in naturally occurring O‐heterocycles

inferredcites →https://doi.org/10.1007/s10086-007-0892-xopenalex-snapshot

Biosynthesis of lignans and norlignans

inferredcites →https://doi.org/10.1007/s12272-012-1005-yopenalex-snapshot

Phenylpropanoids and lignanoids from Euonymus acanthocarpus

inferredcites →https://doi.org/10.1016/0031-9422(80)83107-4openalex-snapshot

A new neolignan and other phenolic constituents from Cedrus deodara

inferredcites →https://doi.org/10.1016/0031-9422(90)80144-6openalex-snapshot

Flavanone xyloside and lignans from Prunus jamasakura bark

inferredcites →https://doi.org/10.1016/0031-9422(95)00072-fopenalex-snapshot

Lignans from the wood of Aralia bipinnata

inferredcites →https://doi.org/10.1016/j.bmcl.2012.01.062openalex-snapshot

New antitumor compounds from Carya cathayensis

inferredcites →https://doi.org/10.1016/j.bmcl.2015.03.015openalex-snapshot

(+)- and (−)-liriodenol, a pair of novel enantiomeric lignans from Liriodendron hybrid

inferredcites →https://doi.org/10.1016/j.bse.2013.06.004openalex-snapshot

Chemical constituents from Metasequoia glyptostroboides Hu et Cheng

inferredcites →https://doi.org/10.1016/j.bse.2014.03.030openalex-snapshot

Neolignans from the seeds of Prunus tomentosa (Rosaceae) and their chemotaxonomic interest

inferredcites →https://doi.org/10.1016/j.bse.2014.04.016openalex-snapshot

Phytochemical and chemotaxonomic studies on Phyllanthus urinaria

inferredcites →https://doi.org/10.1016/j.fbp.2010.04.008openalex-snapshot

A review of the antioxidant potential of medicinal plant species

inferredcites →https://doi.org/10.1016/j.phytochem.2007.08.022openalex-snapshot

Neolignan glycosides from Symplocos caudata

inferredcites →https://doi.org/10.1016/j.phytochem.2008.04.002openalex-snapshot

Trypanocidal structure–activity relationship for cis- and trans-methylpluviatolide

inferredcites →https://doi.org/10.1016/j.phytochem.2011.04.007openalex-snapshot

Schistosomicidal and trypanocidal structure–activity relationships for (±)-licarin A and its (−)- and (+)-enantiomers

inferredcites →https://doi.org/10.1016/j.phytochem.2013.10.003openalex-snapshot

Scapiformolactones A–I: Germacrane sesquiterpenoids with an unusual Δ3-15,6-lactone moiety from Salvia scapiformis

inferredcites →https://doi.org/10.1016/j.phytol.2011.09.007openalex-snapshot

New phenolics from the wood of Casearia grewiifolia

inferredcites →https://doi.org/10.1016/j.phytol.2013.11.013openalex-snapshot

A new flavone sulfonic acid from Phyllanthus urinaria

inferredcites →https://doi.org/10.1016/j.tetlet.2013.06.082openalex-snapshot

Phyllanflexoid C: first example of phenylacetylene-bearing 18-nor-diterpenoid glycoside from the roots of Phyllanthus flexuosus

inferredcites →https://doi.org/10.1016/s0031-9422(96)00885-0openalex-snapshot

Heartwood constituents of Betula maximowicziana

inferredcites →https://doi.org/10.1016/s0040-4020(01)92310-5openalex-snapshot

Optical rotatory dispersion and circular dichroism or aromatic compounds: a general survey

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Modeling NMR Parameters by DFT Methods as an Aid to the Conformational Analysis of cis-Fused 7a(8a)-Methyl Octa(hexa)hydrocyclopenta[d][1,3]oxazines and [3,1]benzoxazines

inferredcites →https://doi.org/10.1021/ja105035ropenalex-snapshot

Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability

inferredcites →https://doi.org/10.1021/ja511813gopenalex-snapshot

Phainanoids A–F, A New Class of Potent Immunosuppressive Triterpenoids with an Unprecedented Carbon Skeleton from Phyllanthus hainanensis

inferredcites →https://doi.org/10.1021/jf502171zopenalex-snapshot

Antioxidant and Anti-inflammatory Active Dihydrobenzofuran Neolignans from the Seeds of Prunus tomentosa

inferredcites →https://doi.org/10.1021/jo5004604openalex-snapshot

Anti-Hepatitis B Virus Norbisabolane Sesquiterpenoids from Phyllanthus acidus and the Establishment of Their Absolute Configurations Using Theoretical Calculations

inferredcites →https://doi.org/10.1021/np010370gopenalex-snapshot

Phyllanemblinins A−F, New Ellagitannins from Phyllanthus e mblica

inferredcites →https://doi.org/10.1021/np200117yopenalex-snapshot

Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations

inferredcites →https://doi.org/10.1021/np5002785openalex-snapshot

Potent Cytotoxic Arylnaphthalene Lignan Lactones from Phyllanthus poilanei

inferredcites →https://doi.org/10.1021/np500528uopenalex-snapshot

(±)-Torreyunlignans A–D, Rare 8–9′ Linked Neolignan Enantiomers as Phosphodiesterase-9A Inhibitors from Torreya yunnanensis

inferredcites →https://doi.org/10.1021/np50060a011openalex-snapshot

Alkaloids from the Leaves of Phyllanthus discoideus

inferredcites →https://doi.org/10.1021/np5010533openalex-snapshot

Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium

inferredcites →https://doi.org/10.1021/np900712vopenalex-snapshot

Neolignans and Glycosides from the Stem Bark of Illicium difengpi

inferredcites →https://doi.org/10.1021/np980003dopenalex-snapshot

Isolation and Absolute Structures of Enantiomeric 1,2-Bis(4-hydroxy-3-methoxyphenyl)-1,3-propanediol 1-O-Glucosides from the Bark of Hovenia trichocarpa

inferredcites →https://doi.org/10.1021/ol502649aopenalex-snapshot

Chiral Resolution and Absolute Configuration of a Pair of Rare Racemic Spirodienone Sesquineolignans from Xanthium sibiricum

inferredcites →https://doi.org/10.1021/ol5030579openalex-snapshot

Bioactive Acylphloroglucinols with Adamantyl Skeleton from Hypericum sampsonii

inferredcites →https://doi.org/10.1038/ki.2011.341openalex-snapshot

Antioxidant therapy in hemodialysis patients: a systematic review

inferredcites →https://doi.org/10.1038/mp.2014.111openalex-snapshot

Traumatic stress, oxidative stress and post-traumatic stress disorder: neurodegeneration and the accelerated-aging hypothesis

inferredcites →https://doi.org/10.1038/nrd4002openalex-snapshot

Modulation of oxidative stress as an anticancer strategy

inferredcites →https://doi.org/10.1038/nrrheum.2013.147openalex-snapshot

Oxidative stress in the pathology and treatment of systemic lupus erythematosus

inferredcites →https://doi.org/10.1039/b514045popenalex-snapshot

An update on bioactive plant lignans

inferredcites →https://doi.org/10.1039/b910940dopenalex-snapshot

An update on lignans: natural products and synthesis

inferredcites →https://doi.org/10.1039/c4ra16624hopenalex-snapshot

Stereochemistry of cleistanthane diterpenoid glucosides from Phyllanthus emblica

inferredcites →https://doi.org/10.1080/10286020.2013.848429openalex-snapshot

Two new compounds from Crataegus pinnatifida and their antithrombotic activities

inferredcites →https://doi.org/10.1080/14786419.2015.1023198openalex-snapshot

New cytotoxic lignan glycosides fromPhyllanthus glaucus

inferredcites →https://doi.org/10.1203/pdr.0b013e3181a9eafbopenalex-snapshot

Oxygen Toxicity and Reactive Oxygen Species: The Devil Is in the Details

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Medicinal Foodstuffs. XXXI. Structures of New Aromatic Constituents and Inhibitors of Degranulation in RBL-2H3 Cells from a Japanese Folk Medicine, the Stem Bark of Acer nikoense.

inferredcites →https://doi.org/10.1515/znb-2006-1018openalex-snapshot

Lignans from the Roots and Rhizomes of Clematis manshurica

inferredcites →https://doi.org/10.2174/0929867033456828openalex-snapshot

Contribution of Reactive Oxygen Species to Cartilage Degradation in Rheumatic Diseases: Molecular Pathways, Diagnosis and Potential Therapeutic Strategies

inferredcites →https://doi.org/10.3724/sp.j.1009.2011.00115openalex-snapshot

Chemical Constituents of Toona ciliata var. pubescens

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Lignans from the seeds of Herpetospermum pedunculosum and their farnesoid X receptor-activating effect

inferred← citeshttps://doi.org/10.1002/9783527825578.c02-67openalex-snapshot

Phyllanthus Species

inferred← citeshttps://doi.org/10.1002/cbdv.202100231openalex-snapshot

Lignans from Lepidium meyenii and Their Anti‐Inflammatory Activities

inferred← citeshttps://doi.org/10.1002/cbdv.202402483openalex-snapshot

An Updated Review on the Anti‐Inflammatory Potential of Phyllanthus Genus

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Chemical Constituents from Ethanoic Extracts of the Aerial Parts of Leea aequata L., a Traditional Folk Medicine of Myanmar

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In vitro hepatoprotective lignan production from Phyllanthus species

inferred← citeshttps://doi.org/10.1016/b978-0-443-30170-4.00011-5openalex-snapshot

Chemistry and pharmacology of lignans and stilbenes reported in African medicinal plants

inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.05.016openalex-snapshot

Discovery of dihydrobenzofuran neolignans from Rubus ideaus L. with enantioselective anti-Aβ1–42 aggregation activity

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Stereoisomeric guaiacylglycerol-β-coniferyl aldehyde ether induces distinctive apoptosis by downregulation of MEK/ERK pathway in hepatocellular carcinoma cells

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Chiral resolution and neuroprotective activities of enantiomeric dihydrobenzofuran neolignans from the fruit of Crataegus pinnatifida

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Synthesis of novel derivatives from machilin C/D as antiproliferative agents against triple negative breast cancer

inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116445openalex-snapshot

Sesquilignans: Current research and potential prospective

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.10.022openalex-snapshot

Azacoccones A − E, five new aza-epicoccone derivatives from Aspergillus flavipes

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.12.010openalex-snapshot

Seven new sesquineolignans isolated from the seeds of hawthorn and their neuroprotective activities

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.01.012openalex-snapshot

Chiral resolution and bioactivity of enantiomeric benzofuran neolignans from the fruit of Rubus ideaus L.

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.05.006openalex-snapshot

Phenylacetylene-bearing 3,4-seco-cleistanthane diterpenoids from the roots of Phyllanthus glaucus

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.06.014openalex-snapshot

Novel sesquilignan and lignan glycoside from the twigs and leaves of Illicium majus

inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104287openalex-snapshot

Racemic neolignans from Crataegus pinnatifida: Chiral resolution, configurational assignment, and cytotoxic activities against human hepatoma cells

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104591openalex-snapshot

Sesquineolignans derivatives with neuroprotective activity from the fruits of Crataegus pinnatifida

inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105701openalex-snapshot

Aromatic glycosides and lignans glycosides with their acetylcholinesterase inhibitory activities from the leaves of Picrasma quassioides

inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.09.065openalex-snapshot

A novel alkaloid isolated from Crotalaria paulina and identified by NMR and DFT calculations

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Chiral separation of sesquineolignans from the stems and leaves of Neoshirakia japonica

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Two new compounds from the aerial parts of Stelleropsis tianschanica and their cytotoxic activity

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Two new norneolignans and other components from Strophioblachia fimbricalyx

inferred← citeshttps://doi.org/10.1016/s1674-6384(17)60095-9openalex-snapshot

Triterpenoids from Whole Plants of Phyllanthus urinaria

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Neolignans from Red Raspberry (Rubus idaeus L.) Exhibit Enantioselective Neuroprotective Effects against H2O2-Induced Oxidative Injury in SH-SY5Y Cells

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Phenolics and Phenolic Glycosides from Wrightia pubescens and Their Hepatoprotective Activities

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Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line

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Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00670openalex-snapshot

Acylated Lignans Isolated from Brachanthemum gobicum and Their Trypanocidal Activity

inferred← citeshttps://doi.org/10.1038/s41598-017-15423-4openalex-snapshot

LC-MS guided isolation of three pairs of enantiomeric alkaloids from Macleaya cordata and their enantioseparations, antiproliferative activity, apoptosis-inducing property

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Bioassay-guided isolation of hepatoprotective lignans from Vernonia cinerea : DeepSAT-driven structural elucidation and predictive mechanistic insights against drug-induced liver injury

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Threo-2,3-bis-(4-hydroxy-3-methoxyphenyl)-3-methoxypropanol (THMP) Inhibits Bladder Cancer Cell Proliferation via Oxidative Stress-dependent Apoptosis and DNA Damage

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Two new sesquineolignans from the seeds of Crataegus pinnatifida and their β-amyloid aggregation inhibitory activitiy

inferred← citeshttps://doi.org/10.1080/14786419.2019.1577839openalex-snapshot

Chiral resolution and bioactivity of enantiomeric furofuran lignans from Juglans mandshurica Maxim

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Thermal priming enhances heat tolerance in alfalfa (Medicago sativa L.) through activation of multiple metabolic pathways

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Chemical Components and Biological Activities of the Genus Phyllanthus: A Review of the Recent Literature

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Natural Enantiomers: Occurrence, Biogenesis and Biological Properties

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