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Recent advances in research on lignans and neolignans
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201408641openalex-snapshot
A Bio‐Inspired Total Synthesis of Tetrahydrofuran Lignans
inferredcites →https://doi.org/10.1002/ardp.200300841openalex-snapshot
Two New Arylnaphthalide Lignans and Antiplatelet Constituents from Justicia procumbens
inferredcites →https://doi.org/10.1002/ejoc.200400700openalex-snapshot
The Use of Tosylhydrazone Salts as a Safe Alternative for Handling Diazo Compounds and Their Applications in Organic Synthesis
inferredcites →https://doi.org/10.1002/hlca.201500002openalex-snapshot
Three New Lignan Derivatives from Lindera glauca ( Siebold et Zucc .) Blume
inferredcites →https://doi.org/10.1007/s00404-011-2120-6openalex-snapshot
Antiproliferative activity of lignans against the breast carcinoma cell lines MCF 7 and BT 20
inferredcites →https://doi.org/10.1007/s11010-012-1487-4openalex-snapshot
Investigation of in vitro and in vivo antioxidant potential of secoisolariciresinol diglucoside
inferredcites →https://doi.org/10.1007/s11101-013-9311-7openalex-snapshot
Isolation of lignans as seed germination and plant growth inhibitors from Mediterranean plants and chemical synthesis of some analogues
inferredcites →https://doi.org/10.1007/s12272-009-1404-xopenalex-snapshot
A new furofuran lignan from Isodon japonicus
inferredcites →https://doi.org/10.1007/s12272-011-1206-9openalex-snapshot
A new lignan glycoside from Juniperus rigida
inferredcites →https://doi.org/10.1016/0166-3542(95)00020-mopenalex-snapshot
Differential inhibition of reverse transcriptase and cellular DNA polymerase-α activities by lignans isolated from Chinese herbs, Phyllanthus myrtifolius Moon, and tannins from Lonicera japonica Thunb and Castanopsis hystrix
inferredcites →https://doi.org/10.1016/j.antiviral.2009.11.002openalex-snapshot
Lignan, sesquilignans and dilignans, novel HIV-1 protease and cytopathic effect inhibitors purified from the rhizomes of Saururus chinensis
inferredcites →https://doi.org/10.1016/j.apsb.2013.02.004openalex-snapshot
A new lignan and active compounds inhibiting NF-κB signaling pathway from Caulis Trachelospermi
inferredcites →https://doi.org/10.1016/j.bioorg.2013.06.009openalex-snapshot
Lignans of sesame: Purification methods, biological activities and biosynthesis – A review
inferredcites →https://doi.org/10.1016/j.bmc.2009.06.010openalex-snapshot
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity
inferredcites →https://doi.org/10.1016/j.bmc.2009.10.031openalex-snapshot
Derivatives of schisandrin with increased inhibitory potential on prostaglandin E2 and leukotriene B4 formation in vitro
inferredcites →https://doi.org/10.1016/j.bmcl.2008.11.103openalex-snapshot
In vitro anti-inflammatory activity of lignans isolated from Magnolia fargesii
inferredcites →https://doi.org/10.1016/j.bmcl.2009.07.078openalex-snapshot
Schisanwilsonins A–G and related anti-HBV lignans from the fruits of Schisandra wilsoniana
inferredcites →https://doi.org/10.1016/j.bmcl.2010.10.135openalex-snapshot
Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production
inferredcites →https://doi.org/10.1016/j.bmcl.2011.02.102openalex-snapshot
Inhibition of nitric oxide production in lipopolysaccharide-stimulated RAW264.7 macrophage cells by lignans isolated from Euonymus alatus leaves and twigs
inferredcites →https://doi.org/10.1016/j.bmcl.2011.04.036openalex-snapshot
Three new cytotoxic aryltetralin lignans from Sinopodophyllum emodi
inferredcites →https://doi.org/10.1016/j.bmcl.2011.09.014openalex-snapshot
Synthesis and evaluation of cytotoxic effects of hanultarin and its derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2011.12.072openalex-snapshot
Enzymatic transformation of caffeic acid with enhanced cyclooxygenase-2 inhibitory activity
inferredcites →https://doi.org/10.1016/j.bmcl.2012.08.016openalex-snapshot
Phenolic constituents from the rhizomes of Acorus gramineus and their biological evaluation on antitumor and anti-inflammatory activities
inferredcites →https://doi.org/10.1016/j.bmcl.2013.01.046openalex-snapshot
Anti-hepatitis B virus lignans from the root of Streblus asper
inferredcites →https://doi.org/10.1016/j.bmcl.2013.07.062openalex-snapshot
Synthesis and antioxidant evaluation of (S,S)- and (R,R)-secoisolariciresinol diglucosides (SDGs)
inferredcites →https://doi.org/10.1016/j.bmcl.2013.08.004openalex-snapshot
Anti-inflammatory constituents from the fruits of Vitex rotundifolia
inferredcites →https://doi.org/10.1016/j.bmcl.2013.08.011openalex-snapshot
Corrigendum to “Two dimeric lignans with an unusual α,β-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production” [Bioorg. Med. Chem. Lett. 21 (2011) 373–376]
inferredcites →https://doi.org/10.1016/j.bmcl.2013.08.045openalex-snapshot
The cytotoxicity of 8-O-4′ neolignans from the seeds of Crataegus pinnatifida
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.2014.02.030openalex-snapshot
A novel neolignan glycoside from Aquilaria sinensis
inferredcites →https://doi.org/10.1016/j.cclet.2010.09.001openalex-snapshot
A new aryltetrahydronaphthalene lignan from Epimedium brevicornum
inferredcites →https://doi.org/10.1016/j.cclet.2010.10.013openalex-snapshot
Lignan glucoside from Sinopodophyllum emodi and its cytotoxic activity
inferredcites →https://doi.org/10.1016/j.cclet.2013.11.053openalex-snapshot
Two new eupodienone lignans from Gymnotheca chinensis
inferredcites →https://doi.org/10.1016/j.chembiol.2012.06.004openalex-snapshot
Chemical Ecology of Endophytic Fungi: Origins of Secondary Metabolites
inferredcites →https://doi.org/10.1016/j.fct.2012.07.014openalex-snapshot
Lignan constituents of Tilia amurensis and their biological evaluation on antitumor and anti-inflammatory activities
inferredcites →https://doi.org/10.1016/j.fct.2013.08.046openalex-snapshot
New inhibitors of nitric oxide production from the seeds of Myristica fragrans
inferredcites →https://doi.org/10.1016/j.fitote.2009.08.024openalex-snapshot
Study of anti-inflammatory, analgesic and antipyretic activities of seeds of Hyoscyamus niger and isolation of a new coumarinolignan
inferredcites →https://doi.org/10.1016/j.fitote.2010.08.008openalex-snapshot
Neolignans and flavonoids from the root bark of Illicium henryi
inferredcites →https://doi.org/10.1016/j.fitote.2012.01.009openalex-snapshot
Anti-HBV activities of Streblus asper and constituents of its roots
inferredcites →https://doi.org/10.1016/j.fitote.2012.03.020openalex-snapshot
Phenolics from Leontopodium leontopodioides inhibiting nitric oxide production
inferredcites →https://doi.org/10.1016/j.fitote.2012.12.028openalex-snapshot
Neolignans from leaves of Miliusa mollis
inferredcites →https://doi.org/10.1016/j.fitote.2013.04.002openalex-snapshot
Simonols A and B, two novel sesqui-neolignans from the fruits of Illicium simonsii
inferredcites →https://doi.org/10.1016/j.fitote.2013.08.009openalex-snapshot
Diastereomers of lithospermic acid and lithospermic acid B from Monarda fistulosa and Lithospermum erythrorhizon
inferredcites →https://doi.org/10.1016/j.fitote.2013.08.011openalex-snapshot
8-9′ linked neolignans with cytotoxicity from Alpinia conchigera
inferredcites →https://doi.org/10.1016/j.fitote.2013.09.011openalex-snapshot
Cytotoxic and antioxidant dihydrobenzofuran neolignans from the seeds of Crataegus pinnatifida
inferredcites →https://doi.org/10.1016/j.fitote.2014.01.025openalex-snapshot
Cytotoxic activity of lignans from Justicia procumbens
inferredcites →https://doi.org/10.1016/j.fitote.2014.09.008openalex-snapshot
Neolignans, lignans and glycoside from the fruits of Melia toosendan
inferredcites →https://doi.org/10.1016/j.fitote.2014.11.006openalex-snapshot
Penthorin A and B, two unusual 2,4′-epoxy-8,5′-neolignans from Penthorum chinese
inferredcites →https://doi.org/10.1016/j.fitote.2014.12.011openalex-snapshot
Two new lignans from Saururus chinensis and their DGAT inhibitory activity
inferredcites →https://doi.org/10.1016/j.fitote.2015.01.008openalex-snapshot
Antimicrobial and cytotoxic phenolics and phenolic glycosides from Sargentodoxa cuneata
inferredcites →https://doi.org/10.1016/j.fitote.2015.03.011openalex-snapshot
Lignans from the root of Paeonia lactiflora and their anti-β-amyloid aggregation activities
inferredcites →https://doi.org/10.1016/j.fitote.2015.03.015openalex-snapshot
New lignans from the roots of Schisandra sphenanthera
inferredcites →https://doi.org/10.1016/j.fitote.2015.05.010openalex-snapshot
Phenylpropanoids and neolignans from Smilax trinervula
inferredcites →https://doi.org/10.1016/j.foodchem.2009.04.057openalex-snapshot
Identification and distribution of lignans in Punica granatum L. fruit endocarp, pulp, seeds, wood knots and commercial juices by GC–MS
inferredcites →https://doi.org/10.1016/j.foodchem.2012.11.062openalex-snapshot
Root tubers of Lactuca tuberosa as a source of antioxidant phenolic compounds and new furofuran lignans
inferredcites →https://doi.org/10.1016/j.foodchem.2014.09.170openalex-snapshot
New neolignans from the seeds of Myristica fragrans that inhibit nitric oxide production
inferredcites →https://doi.org/10.1016/j.jep.2005.06.041openalex-snapshot
Euonymus alatus prevents the hyperglycemia and hyperlipidemia induced by high-fat diet in ICR mice
inferredcites →https://doi.org/10.1016/j.jphotobiol.2013.08.002openalex-snapshot
Isolation and characterization of bioactive compounds from the bark of Litsea costalis
inferredcites →https://doi.org/10.1016/j.phymed.2012.07.017openalex-snapshot
Chemical analysis of twelve lignans in the fruit of Schisandra sphenanthera by HPLC–PAD-MS
inferredcites →https://doi.org/10.1016/j.phytochem.2008.11.005openalex-snapshot
Dibenzocyclooctadiene lignans from Kadsura philippinensis
inferredcites →https://doi.org/10.1016/j.phytochem.2009.05.016openalex-snapshot
Glycosides of arylnaphthalene lignans from Acanthus mollis having axial chirality
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.010openalex-snapshot
PAF-antagonistic bicyclo[3.2.1]octanoid neolignans from leaves of Ocotea macrophylla Kunth. (Lauraceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.021openalex-snapshot
Gentisic acid conjugates of Medicago truncatula roots
inferredcites →https://doi.org/10.1016/j.phytochem.2009.07.029openalex-snapshot
Antihyperglycemic activity of phenylpropanoyl esters of catechol glycoside and its dimers from Dodecadenia grandiflora
inferredcites →https://doi.org/10.1016/j.phytochem.2009.12.008openalex-snapshot
Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses
inferredcites →https://doi.org/10.1016/j.phytochem.2010.06.014openalex-snapshot
Dibenzocyclooctadiene lignans from Magnolia and Talauma (Magnoliaceae): Their absolute configuration ascertained by circular dichroism and X-ray crystallography and re-evaluation of previously published pyramidatin structures
inferredcites →https://doi.org/10.1016/j.phytochem.2010.06.015openalex-snapshot
Lignans in flowering aerial parts of Linum species – Chemodiversity in the light of systematics and phylogeny
inferredcites →https://doi.org/10.1016/j.phytochem.2011.05.008openalex-snapshot
Triterpenes and neolignans from the roots of Nannoglottis carpesioides
inferredcites →https://doi.org/10.1016/j.phytochem.2011.09.019openalex-snapshot
An unusual caffeic acid derived bicyclic [2.2.2] octane lignan and other constituents from Cordia rufescens
inferredcites →https://doi.org/10.1016/j.phytochem.2012.06.023openalex-snapshot
Anti-hepatitis B virus constituents from the stem bark of Streblus asper
inferredcites →https://doi.org/10.1016/j.phytochem.2013.03.008openalex-snapshot
Neolignans and phenylpropanoids from the roots of Piper taiwanense and their antiplatelet and antitubercular activities
inferredcites →https://doi.org/10.1016/j.phytochem.2013.07.022openalex-snapshot
Antioxidant lignoids from leaves of Ribes nigrum
inferredcites →https://doi.org/10.1016/j.phytochem.2014.04.014openalex-snapshot
Dibenzocyclooctadiene lignans from Schisandra chinensis and their inhibitory activity on NO production in lipopolysaccharide-activated microglia cells
inferredcites →https://doi.org/10.1016/j.phytochem.2014.10.032openalex-snapshot
Hispidacine, an unusual 8,4′-oxyneolignan-alkaloid with vasorelaxant activity, and hispiloscine, an antiproliferative phenanthroindolizidine alkaloid, from Ficus hispida Linn.
inferredcites →https://doi.org/10.1016/j.phytochem.2015.03.009openalex-snapshot
Isolation and anti-hepatitis B virus activity of dibenzocyclooctadiene lignans from the fruits of Schisandra chinensi s
inferredcites →https://doi.org/10.1016/j.phytochem.2015.06.012openalex-snapshot
Chemical constituents of Abies fabri
inferredcites →https://doi.org/10.1016/j.phytochem.2015.10.002openalex-snapshot
Phenylpropanoid and lignan glycosides from the aerial parts of Lespedeza cuneata
inferredcites →https://doi.org/10.1016/j.phytol.2010.12.006openalex-snapshot
Lignans from Phillyrea angustifolia L.
inferredcites →https://doi.org/10.1016/j.phytol.2011.03.007openalex-snapshot
Phytochemical and bioactivity studies on constituents of the leaves of Vitex quinata
inferredcites →https://doi.org/10.1016/j.phytol.2011.08.010openalex-snapshot
Neolignans from Callistemon lanceolatus
inferredcites →https://doi.org/10.1016/j.phytol.2012.01.003openalex-snapshot
Two new neolignan glycosides from Pittosporum glabratum Lindl.
inferredcites →https://doi.org/10.1016/j.phytol.2012.02.004openalex-snapshot
Two pairs of new diastereoisomeric flavonolignans from the seeds of Hovenia acerba
inferredcites →https://doi.org/10.1016/j.phytol.2012.12.008openalex-snapshot
Lignans from the fruit of Schisandra sphenanthera, and their inhibition of HSV-2 and adenovirus
inferredcites →https://doi.org/10.1016/j.phytol.2013.06.004openalex-snapshot
New ellagitannin and galloyl esters of phenolic glycosides from sapwood of Quercus mongolica var. crispula (Japanese oak)
inferredcites →https://doi.org/10.1016/j.phytol.2014.06.005openalex-snapshot
Lignans from the roots of Kadsura coccinea and their inhibitory activities on LPS-induced NO production
inferredcites →https://doi.org/10.1016/j.phytol.2014.12.004openalex-snapshot
Bioactive lignans from Zanthoxylum planispinum with cytotoxic potential
inferredcites →https://doi.org/10.1016/j.phytol.2015.06.001openalex-snapshot
Aryltetralols from Holostylis reniformis and syntheses of lignan analogous
inferredcites →https://doi.org/10.1016/j.procbio.2015.01.023openalex-snapshot
Identification and isolation of new neolignan and sesquineolignan species: Their acid-catalyzed ring closure and specific accumulation in the fruit wall of Cirsium eriophorum (L.) Scop.
inferredcites →https://doi.org/10.1016/j.talanta.2010.12.025openalex-snapshot
Identification and quantification of lignans in wheat bran by gas chromatography-electron capture detection
inferredcites →https://doi.org/10.1016/j.tet.2011.03.019openalex-snapshot
Uragogin and blepharodin, unprecedented hetero-Diels–Alder adducts from Celastraceae species
inferredcites →https://doi.org/10.1016/j.tet.2011.04.105openalex-snapshot
New dibenzocyclooctadiene lignans from the Kadsura ananosma
inferredcites →https://doi.org/10.1016/j.tet.2013.04.086openalex-snapshot
Rh(II)-catalyzed enantioselective synthesis of acuminatin through a C–H insertion reaction of a non-stabilized carbenoid
inferredcites →https://doi.org/10.1016/j.tetlet.2013.05.144openalex-snapshot
New neolignans and a lignan from Miliusa fragrans, and their anti-herpetic and cytotoxic activities
inferredcites →https://doi.org/10.1016/j.tetlet.2013.06.109openalex-snapshot
A cytotoxic decahydronaphthalenylpropenal derivative and tetrahydrofuran lignans from the stems of Cameraria latifolia
inferredcites →https://doi.org/10.1016/s0031-9422(01)00100-5openalex-snapshot
Bioactive Compounds from Natural Sources: Isolation, Characterisation and Biological Properties
inferredcites →https://doi.org/10.1016/s0378-8741(98)00042-7openalex-snapshot
Central inhibitory effects of water extract of Acori graminei rhizoma in mice
inferredcites →https://doi.org/10.1021/acs.jafc.5b02838openalex-snapshot
New Butyrolactone Type Lignans from Arctii Fructus and Their Anti-inflammatory Activities
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00220openalex-snapshot
Neolignans from Aristolochia fordiana Prevent Oxidative Stress-Induced Neuronal Death through Maintaining the Nrf2/HO-1 Pathway in HT22 Cells
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00328openalex-snapshot
(±)-Acortatarinowins A–F, Norlignan, Neolignan, and Lignan Enantiomers from Acorus tatarinowii
inferredcites →https://doi.org/10.1021/jf053048aopenalex-snapshot
Antioxidant Potentials of Flaxseed by in Vivo Model
inferredcites →https://doi.org/10.1021/jf100323qopenalex-snapshot
Lignans from the Tuber-barks of Colocasia antiquorum var. esculenta and Their Antimelanogenic Activity
inferredcites →https://doi.org/10.1021/jf1041933openalex-snapshot
Isolation and Identification of Compounds Responsible for Antioxidant Capacity of Euryale ferox Seeds
inferredcites →https://doi.org/10.1021/jf202119mopenalex-snapshot
Antioxidant and Tyrosinase Inhibitory Constituents from a Desugared Sugar Cane Extract, a Byproduct of Sugar Production
inferredcites →https://doi.org/10.1021/jf204660copenalex-snapshot
Lignans from the Root of Rhodiola crenulata
inferredcites →https://doi.org/10.1021/jf4007104openalex-snapshot
Recent Advances in the Metabolic Engineering of Lignan Biosynthesis Pathways for the Production of Transgenic Plant-Based Foods and Supplements
inferredcites →https://doi.org/10.1021/jf501859xopenalex-snapshot
Hepatoprotective Activity of Twelve Novel 7′-Hydroxy Lignan Glucosides from Arctii Fructus
inferredcites →https://doi.org/10.1021/jo010779aopenalex-snapshot
Asymmetric Syntheses of New Functionalized β-Amino Alcohols via Diastereoselective Addition of Organometallic Reagents onto Oxazolidines
inferredcites →https://doi.org/10.1021/jo1022712openalex-snapshot
Glucokinase-Activating Sesquinlignans from the Rhizomes of Acorus tatarinowii Schott
inferredcites →https://doi.org/10.1021/jo301225vopenalex-snapshot
Gymnothelignans A–O: Conformation and Absolute Configuration Analyses of Lignans Bearing Tetrahydrofuran from Gymnotheca chinensis
inferredcites →https://doi.org/10.1021/jo962423iopenalex-snapshot
Shortcut Syntheses of Naturally Occurring 5-Alkylresorcinols with DNA-Cleaving Properties
inferredcites →https://doi.org/10.1021/jo990263fopenalex-snapshot
Novel C19 Homolignans, Taiwanschirin A, B, and Cytotoxic Taiwanschirin C, and a New C18 Lignan, Schizanrin A, from Schizandra arisanensis
inferredcites →https://doi.org/10.1021/np0600447openalex-snapshot
Bioactive Secolignans from Peperomia dindygulensis
inferredcites →https://doi.org/10.1021/np100067wopenalex-snapshot
Dibenzocyclooctadiene Lignans from Schisandra wilsoniana and Their Anti-HIV-1 Activities
inferredcites →https://doi.org/10.1021/np100263eopenalex-snapshot
Substituted Dineolignans from Magnolia garrettii
inferredcites →https://doi.org/10.1021/np100332vopenalex-snapshot
Lignans and Triterpenes from the Bark of Durio carinatus and Durio oxleyanus
inferredcites →https://doi.org/10.1021/np1005357openalex-snapshot
Caffeic Acid Esters and Lignans from Piper sanguineispicum
inferredcites →https://doi.org/10.1021/np100607sopenalex-snapshot
Microbial Transformations of Aryltetralone and Aryltetralin Lignans by Cunninghamella echinulata and Beauveria bassiana
inferredcites →https://doi.org/10.1021/np1007476openalex-snapshot
An Unprecedented Neolignan Skeleton from Chimarrhis turbinata
inferredcites →https://doi.org/10.1021/np100891yopenalex-snapshot
Spirocyclic Lignans from Guaiacum (Zygophyllaceae) Induce Apoptosis in Human Breast Cancer Cell Lines
inferredcites →https://doi.org/10.1021/np1009288openalex-snapshot
Dibenzocyclooctadiene Lignans with Antineurodegenerative Potential from Kadsura ananosma
inferredcites →https://doi.org/10.1021/np200117yopenalex-snapshot
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations
inferredcites →https://doi.org/10.1021/np2001896openalex-snapshot
Bioactive Neolignans and Lignans from the Bark of Machilus robusta
inferredcites →https://doi.org/10.1021/np200279ropenalex-snapshot
Anti-inflammatory Endiandric Acid Analogues from the Roots of Beilschmiedia tsangii
inferredcites →https://doi.org/10.1021/np200541mopenalex-snapshot
Bioactive Lignans from the Rhizomes of Acorus gramineus
inferredcites →https://doi.org/10.1021/np200678nopenalex-snapshot
Phenolic Glycosides from Sugar Maple (Acer saccharum) Bark
inferredcites →https://doi.org/10.1021/np200937hopenalex-snapshot
Dibenzocyclooctadiene Lignans fromKadsura polyspermaand Their Antineurodegenerative Activities
inferredcites →https://doi.org/10.1021/np3003832openalex-snapshot
Cytotoxic Lignans from Fruits of Cleistanthus indochinensis: Synthesis of Cleistantoxin Derivatives
inferredcites →https://doi.org/10.1021/np300699fopenalex-snapshot
Anti-inflammatory Diterpenoids from Croton tonkinensis
inferredcites →https://doi.org/10.1021/np300745qopenalex-snapshot
Dibenzocyclooctadiene Lignans and Norlignans from Fruits of Schisandra wilsoniana
inferredcites →https://doi.org/10.1021/np3007638openalex-snapshot
Antioxidant Lignans and Chromone Glycosides from Eurya japonica
inferredcites →https://doi.org/10.1021/np400070xopenalex-snapshot
Bioactive Dibenzocyclooctadiene Lignans from the Stems of Schisandra neglecta
inferredcites →https://doi.org/10.1021/np4005322openalex-snapshot
Bioactive Lignans from the Trunk of Abies holophylla
inferredcites →https://doi.org/10.1021/np400533hopenalex-snapshot
Protein Tyrosine Phosphatase 1B (PTP1B) Inhibitors from Morinda citrifolia (Noni) and Their Insulin Mimetic Activity
inferredcites →https://doi.org/10.1021/np400772hopenalex-snapshot
Lignans from the Aerial Parts of Saururus chinensis: Isolation, Structural Characterization, and Their Effects on Platelet Aggregation
inferredcites →https://doi.org/10.1021/np500187copenalex-snapshot
Antimicrobial Constituents of the Mature Carpels of Manglietiastrum sinicum
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/np50057a030openalex-snapshot
Justicidin B, a Cytotoxic Principle from Justicia pectoralis
inferredcites →https://doi.org/10.1021/np5008153openalex-snapshot
Neolignans and Other Metabolites from Ocotea cymosa from the Madagascar Rain Forest and Their Biological Activities
inferredcites →https://doi.org/10.1021/np500951sopenalex-snapshot
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum
inferredcites →https://doi.org/10.1021/np800488popenalex-snapshot
Antioxidant Lignans from the Fruits of Broussonetia papyrifera
inferredcites →https://doi.org/10.1021/np900086yopenalex-snapshot
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inferredcites →https://doi.org/10.1021/np900123zopenalex-snapshot
Lignans with Anti-HIV Activity from Schisandra propinqua var. sinensis
inferredcites →https://doi.org/10.1021/np900203yopenalex-snapshot
Constituents of the Leaves of Magnolia ovata
inferredcites →https://doi.org/10.1021/np9003678openalex-snapshot
Oxygenated Lignans from the Fruits of Schisandra arisanensis
inferredcites →https://doi.org/10.1021/np9006298openalex-snapshot
Antiestrogenic Constituents of the Thai Medicinal Plants Capparis flavicans and Vitex glabrata
inferredcites →https://doi.org/10.1021/np900667hopenalex-snapshot
Silver-Catalyzed One-Pot Synthesis of Arylnaphthalene Lactone Natural Products
inferredcites →https://doi.org/10.1021/np9007393openalex-snapshot
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inferredcites →https://doi.org/10.1021/ol8026208openalex-snapshot
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inferredcites →https://doi.org/10.1023/a:1006847310741openalex-snapshot
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inferredcites →https://doi.org/10.1039/b910940dopenalex-snapshot
An update on lignans: natural products and synthesis
inferredcites →https://doi.org/10.1039/b913685aopenalex-snapshot
Advances in the methodology of a multicomponent synthesis of arylnaphthalene lactones
inferredcites →https://doi.org/10.1039/c5np00048copenalex-snapshot
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inferredcites →https://doi.org/10.1055/s-0035-1546127openalex-snapshot
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inferredcites →https://doi.org/10.1055/s-2003-39706openalex-snapshot
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inferredcites →https://doi.org/10.1071/ch9911627openalex-snapshot
Constituents of Eupomatia Species. XIII. The Structures of New Lignans From the Tubers and Aerial Parts of Eupomatia bennettii
inferredcites →https://doi.org/10.1074/jbc.m112.400689openalex-snapshot
Next Generation Sequencing in Predicting Gene Function in Podophyllotoxin Biosynthesis
inferredcites →https://doi.org/10.1080/10286020.2010.543131openalex-snapshot
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inferredcites →https://doi.org/10.1093/chromsci/bmv124openalex-snapshot
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Metabolic Engineering of Lignan Biosynthesis in Forsythia Cell Culture
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The constituents of Schizandra chinensis Baill. I. Isolation and structure determination of five new lignans, gomisin A, B, C, F and G, and the absolute structure of schizandrin.
inferredcites →https://doi.org/10.1248/cpb.27.1395openalex-snapshot
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inferredcites →https://doi.org/10.1351/pac200072081493openalex-snapshot
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inferredcites →https://doi.org/10.3390/molecules17089506openalex-snapshot
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inferredcites →https://doi.org/10.3390/molecules18022297openalex-snapshot
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inferredcites →https://doi.org/10.3390/molecules18066573openalex-snapshot
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inferredcites →https://doi.org/10.3390/molecules18089641openalex-snapshot
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inferredcites →https://doi.org/10.3390/molecules20022165openalex-snapshot
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inferredcites →https://doi.org/10.3762/bjoc.10.313openalex-snapshot
Trogopterins A–C: Three new neolignans from feces of Trogopterus xanthipes
inferredcites →https://doi.org/10.4236/ajps.2011.24072openalex-snapshot
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inferredcites →https://doi.org/10.4236/ajps.2015.65073openalex-snapshot
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inferredcites →https://doi.org/10.5511/plantbiotechnology.12.1230aopenalex-snapshot
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inferredcites →https://doi.org/10.5511/plantbiotechnology.13.0527bopenalex-snapshot
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inferredcites →https://doi.org/10.5511/plantbiotechnology.14.0722aopenalex-snapshot
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inferredcites →https://doi.org/10.5935/0103-5053.20130253openalex-snapshot
Novel Bioactive Dibenzocyclooctadiene Lignans fromSchisandra neglecta
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inferred← citeshttps://doi.org/10.1016/j.addr.2021.113870openalex-snapshot
Multifaceted role of phyto-derived polyphenols in nanodrug delivery systems
inferred← citeshttps://doi.org/10.1016/j.apsb.2023.05.001openalex-snapshot
A new class of potent liver injury protective compounds: Structural elucidation, total synthesis and bioactivity study
inferred← citeshttps://doi.org/10.1016/j.apsb.2023.08.011openalex-snapshot
The ERF transcription factor LTF1 activates DIR1 to control stereoselective synthesis of antiviral lignans and stress defense in Isatis indigotica roots
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105463openalex-snapshot
An integrated strategy for comprehensive characterization of chemical components in Qingqiao Kangdu granules by UHPLC-Q-Exactive-MS coupled with feature-based molecular networking
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2022.105546openalex-snapshot
In vitro evaluation of the antibacterial and cytotoxic activities of the Euclea natalensis crude extract and fractions against oral infection agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.08.033openalex-snapshot
Stereoisomeric guaiacylglycerol-β-coniferyl aldehyde ether induces distinctive apoptosis by downregulation of MEK/ERK pathway in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104093openalex-snapshot
Anti-tyrosinase, anti-cholinesterase and cytotoxic activities of extracts and phytochemicals from the Tunisian Citharexylum spinosum L.: Molecular docking and SAR analysis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105252openalex-snapshot
New lignans from the fruits of Leonurus japonicus and their hepatoprotective activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105492openalex-snapshot
Natural-product-inspired design and synthesis of two series of compounds active against Trypanosoma cruzi: Insights into structure–activity relationship, toxicity, and mechanism of action
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105986openalex-snapshot
Unusual sesquilignans with anti-inflammatory activities from the resin of Ferula sinkiangensis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107732openalex-snapshot
Novel lignans from Syringa pinnatifolia and protective effect against H2O2-induced oxidative injury through regulating the expression of Nrf2/HO-1 in H9c2 cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109189openalex-snapshot
Isolation and bioactivity evaluation of ten novel norlignans and additional neuroprotective compounds from Curculigo gracilis
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.10.145openalex-snapshot
An overview of neuroprotective and cognitive enhancement properties of lignans from Schisandra chinensis
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110714openalex-snapshot
Pleotropic Effects of Polyphenols in Cardiovascular System
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111592openalex-snapshot
The pro-apoptotic properties of a phytonutrient rich infusion of A. cherimola leaf extract on AML cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111963openalex-snapshot
An overview on plants cannabinoids endorsed with cardiovascular effects
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114145openalex-snapshot
Podophyllotoxin and its derivatives: Potential anticancer agents of natural origin in cancer chemotherapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116376openalex-snapshot
Mechanistic insights into the potential role of dietary polyphenols and their nanoformulation in the management of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117486openalex-snapshot
The mechanisms of multidrug resistance of breast cancer and research progress on related reversal agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.07.026openalex-snapshot
Comparative analysis of stilbene and benzofuran neolignan derivatives as acetylcholinesterase inhibitors with neuroprotective and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127354openalex-snapshot
Synthesis and biological evaluation of Schizandrin derivatives as tubulin polymerization inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127413openalex-snapshot
Synthesis of novel lignan-like compounds and their antimicrobial activity
inferred← citeshttps://doi.org/10.1016/j.carbpol.2023.121373openalex-snapshot
Polysaccharide metabolism in Anacardiaceae (Asian lacquer) cross-linked polymers elucidated using in situ trimethylsilylation pyrolysis-gas chromatography–mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.cbi.2019.04.028openalex-snapshot
Eudesmin exerts antitumor effects by down-regulating EZH2 expression in nasopharyngeal carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.cbpa.2020.09.006openalex-snapshot
Synthetic biology for natural product drug production and engineering
inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.102462openalex-snapshot
Functions and mechanisms of enzymes assembling lignans and norlignans
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.110969openalex-snapshot
Palladium-catalyzed modular biomimetic synthesis of lignans derivatives
inferred← citeshttps://doi.org/10.1016/j.chmed.2020.03.006openalex-snapshot
Kadsura coccinea: A rich source of structurally diverse and biologically important compounds
inferred← citeshttps://doi.org/10.1016/j.chmed.2022.03.004openalex-snapshot
Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2021.111724openalex-snapshot
Antiviral zinc oxide nanoparticles mediated by hesperidin and in silico comparison study between antiviral phenolics as anti-SARS-CoV-2
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2018.06.003openalex-snapshot
Tyrosinase inhibition by a rare neolignan: Inhibition kinetics and mechanistic insights through in vitro and in silico studies
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112622openalex-snapshot
Natural sesquiterpenoid oligomers: A chemical perspective
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.119339openalex-snapshot
Photochemical expansion of the dihydrobenzofuran neolignan chemical space enables suppression of c-myc transcription in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.119358openalex-snapshot
Neolignans as emerging anticancer leads: Isolation, chemical diversity, structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173651openalex-snapshot
α-Conidendrin inhibits the expression of intercellular adhesion molecule-1 induced by tumor necrosis factor-α in human lung adenocarcinoma A549 cells
inferred← citeshttps://doi.org/10.1016/j.engmic.2025.100250openalex-snapshot
Effect of resistant starch type 5 on gut health through modulating gut microbiota
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104946openalex-snapshot
The phenylcoumaran benzylic ether reductase gene PtPCBER improves the salt tolerance of transgenic poplar through lignan-mediated reactive oxygen species scavenging
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.110070openalex-snapshot
Development of multi-substrate red yeast rice with no detectable citrinin by co-culture fermentation of Monascus purpureus C5.17 and Saccharomyces cerevisiae: foodomics characterization and metabolic evaluation in diabetic mice
inferred← citeshttps://doi.org/10.1016/j.fct.2019.04.061openalex-snapshot
Activation of TRPC6 channels contributes to (+)-conocarpan-induced apoptotic cell death in HK-2 cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.06.004openalex-snapshot
Furofuran lignans from the Simpson Desert species Eremophila macdonnellii
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.02.019openalex-snapshot
Five new schinortriterpenoids from Schisandra propinqua var. propinqua
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.12.021openalex-snapshot
Biological activity, phytochemistry and traditional uses of genus Lobelia (Campanulaceae): A systematic review
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104403openalex-snapshot
Enantiomeric 8,4′-type oxyneolignans from the root barks of Ailanthus altissima (Mill.) Swingle and their neuroprotective effects against H2O2-induced SH-SY5Y cells injury
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105403openalex-snapshot
Lignans from the genus Piper L. and their pharmacological activities: An updated review
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.105903openalex-snapshot
Undescribed (2–7′)-neolignans and polyoxygenated cyclohexene glycosides from the aerial parts of Piper mutabile C. DC. and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.105982openalex-snapshot
Anti-inflammatory naphthoquinone-monoterpene adducts and neolignans from Eugenia caryophyllata
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106549openalex-snapshot
Aristolochia species (Aristolochiaceae) from the Americas, a review of their traditional medicinal uses, phytochemistry, and pharmacological properties
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106717openalex-snapshot
NMR characterization and anti-inflammatory activity of lignans isolated from the roots of Solanum Verbascifolium L.
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106831openalex-snapshot
Discovery of lignans from leaves of Phyllanthus emblica L. and their antioxidant-antiinflammatory activity
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132464openalex-snapshot
A comprehensive strategy integrating metabolomics with multiple chemometric for discovery of function related active markers for assessment of foodstuffs: A case of hawthorn (Crataegus cuneata) fruits
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.144162openalex-snapshot
Recent insights into functional, structural, and digestibility modifications of starch through complexation with polyphenols: A review
inferred← citeshttps://doi.org/10.1016/j.foodchem.2025.146637openalex-snapshot
Metabolite-based color codes and antioxidant mechanisms in carrots: insights from untargeted metabolomics and bioinformatics
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.116168openalex-snapshot
Foodomics approaches: New insights in phenolic compounds analysis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e22897openalex-snapshot
New lignan glycosides from Justicia secunda Vahl (Acanthaceae) with antimicrobial and antiparasitic properties
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e32899openalex-snapshot
An insight into the anticancer potentials of lignan arctiin: A comprehensive review of molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.hermed.2026.101100openalex-snapshot
Gynaecological healing: exploring traditional ethno-medicinal plants of Himachal Pradesh, India
inferred← citeshttps://doi.org/10.1016/j.indcrop.2019.112077openalex-snapshot
Chemical constituents from temperate and subtropical trees with reference to knotwood
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.116483openalex-snapshot
IiUGT71B2 catalyzes lignan glycosylation in Isatis indigotica with substrates specificity
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102211openalex-snapshot
Pharmaceutically relevant (hetero)cyclic compounds and natural products from lignin-derived monomers: Present and perspectives
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110876openalex-snapshot
Gold-catalyzed highly enantioselective cycloadditions of 1,6-enynes and 1,6-diynes assisted by remote hydrogen bonding interaction
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115148openalex-snapshot
Aconitum carmichaelii Debeaux: A systematic review on traditional use, and the chemical structures and pharmacological properties of polysaccharides and phenolic compounds in the roots
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115819openalex-snapshot
Crataegus pinnatifida: A botanical, ethnopharmacological, phytochemical, and pharmacological overview
inferred← citeshttps://doi.org/10.1016/j.jep.2023.116764openalex-snapshot
Vetiver aerial parts and roots ameliorate rheumatoid arthritis in complete Freund's adjuvant rat model, a phytochemical profiling and mechanistic study
inferred← citeshttps://doi.org/10.1016/j.jff.2017.06.038openalex-snapshot
The Breast Cancer Resistance Protein (BCRP/ABCG2) influences the levels of enterolignans and their metabolites in plasma, milk and mammary gland
inferred← citeshttps://doi.org/10.1016/j.jpba.2018.03.002openalex-snapshot
Qualitative and quantitative analysis of furofuran lignans, iridoid glycosides, and phenolic acids in Radix Dipsaci by UHPLC-Q-TOF/MS and UHPLC-PDA
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2017.01.006openalex-snapshot
Effects of photoperiod regimes and ultraviolet-C radiations on biosynthesis of industrially important lignans and neolignans in cell cultures of Linum usitatissimum L. (Flax)
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153087openalex-snapshot
Increase in cytotoxic lignans production after smut infection in sugar cane plants
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154098openalex-snapshot
Functional analysis of a dirigent protein AtsDIR23 in Acorus tatarinowii
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154138openalex-snapshot
Pour some sugar on me: The diverse functions of phenylpropanoid glycosylation
inferred← citeshttps://doi.org/10.1016/j.mec.2022.e00205openalex-snapshot
A targeted metabolomics method for extra- and intracellular metabolite quantification covering the complete monolignol and lignan synthesis pathway
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130947openalex-snapshot
Synthesis, Characterization, Crystal Structure, Hirshfeld surface analysis and DFT studies of novel compounds based on the methoxynaphthalene ring
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131566openalex-snapshot
Relating the crystal structure and third-order nonlinear susceptibility of a new Neolignan derivative
inferred← citeshttps://doi.org/10.1016/j.phrs.2019.104284openalex-snapshot
Lignans and Neolignans: Plant secondary metabolites as a reservoir of biologically active substances
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.156140openalex-snapshot
A neolignan enantiomer from Piper hancei with anti-neuroinflammatory effect by attenuating NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.phymed.2025.156717openalex-snapshot
The antidiabetic properties of lignans: a comprehensive review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.05.008openalex-snapshot
Isolation of enantiomeric furolactones and furofurans from Rubus idaeus L. with neuroprotective activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112461openalex-snapshot
Lignans and neolignans with isovaleroyloxy moiety from Solanum lyratum Thunb.: Chiral resolution, configurational assignment and neuroprotective effects
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112589openalex-snapshot
Schipropins A–J, structurally diverse triterpenoids from Schisandra propinqua
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113242openalex-snapshot
Naturally occurring dimeric triterpenoids: Occurrence, chemistry and bioactivities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113801openalex-snapshot
Rapid determination of the relative configuration of diverse 8,4′-oxyneolignans by NMR analysis: Retrospective studies, improvement and structural revision
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113913openalex-snapshot
Rare 7,9′-dinorlignans with neuroprotective activity from the roots of Lindera aggregata (Sims) Kosterm
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.113978openalex-snapshot
9,9′-epoxylignans from Syringa pinnatifolia: A typical case of stereochemical assignment by a quantum chemical calculation with MAEΔΔ parameter
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114050openalex-snapshot
Guided isolation of enantiomeric lignans from Cimicifuga heracleifolia Kom. by antioxidant activity and molecular networking
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114132openalex-snapshot
Honokiol and magnolol: A review of structure-activity relationships of their derivatives
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114458openalex-snapshot
Minor dibenzocyclooctadiene lignans with antifibrotic potential from the fruits of Schisandra chinensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114588openalex-snapshot
Eugenol-based meroterpenoids with neural differentiation activity from Eugenia caryophyllata
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114900openalex-snapshot
Obovatollignols A–E, five racemic forms of obovatol-derived dimeric neolignans from Magnolia officinalis var. biloba
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.01.014openalex-snapshot
New bicyclic [3.2.1] octane neolignans derivatives from Aniba firmula with potent in vivo anti-inflammatory activity on account of dual inhibition of PGE2 production and cell recruitment
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.04.013openalex-snapshot
New cyclolignans of Larrea tridentata and their antibacterial and cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.07.015openalex-snapshot
Natural Products Research & The Wealth of Brazilian Biodiversity (NPR & WBB)
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.08.009openalex-snapshot
Bio-active constituents from Schisandra grandiflora: Isolation, semi-synthesis and evaluation of their anticancer activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.07.021openalex-snapshot
Two new norneolignans and other components from Strophioblachia fimbricalyx
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.09.007openalex-snapshot
Justicidin B and related lignans from two South African Monsonia species with potent activity against HeLa cervical cancer cells
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.12.005openalex-snapshot
Laxilignans A-C from the leaves of Terminalia laxiflora Engl. and their α-glucosidase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.phytol.2024.09.002openalex-snapshot
8’,9’-Bis-nor-neolignans from Cedrela odorata and their antiangiogenic activity
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111564openalex-snapshot
Time-resolved transcriptomics reveals ABA-related regulation and phenylpropanoid responses in Herpetospermum pedunculosum roots under salt stress
inferred← citeshttps://doi.org/10.1016/j.procbio.2018.12.025openalex-snapshot
Enhanced production of lignans and neolignans in chitosan-treated flax (Linum usitatissimum L.) cell cultures
inferred← citeshttps://doi.org/10.1016/j.saa.2023.123283openalex-snapshot
Absolute configuration reassignment of nectamazin A: Implications to related neolignans
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.02.017openalex-snapshot
Association of polar fraction of Ageratum conyzoides from the Brazilian Amazon with doxycycline against infection of macrophages with Ehrlichia canis
inferred← citeshttps://doi.org/10.1016/j.sajb.2023.04.043openalex-snapshot
Metabolomic profiling of three Rhododendron species from Eastern Siberia by liquid chromatography with high-resolution mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.021openalex-snapshot
Unusual visible-light photolytic cleavage of tertiary amides during the synthesis of cyclolignans related to podophyllotoxin
inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.005openalex-snapshot
The total synthesis of sevanol, a novel lignan isolated from the thyme plant (Thymus armeniacus)
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132535openalex-snapshot
Highly selective electroreductive linear dimerization of electron-deficient vinylarenes
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133287openalex-snapshot
Catalytic asymmetric synthesis of (−)-arctigenin using a chiral Ir complex
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134887openalex-snapshot
Furofuran lignans involving their unusual oligomers from Indonesian Dysoxylum parasiticum (Osbeck) Kosterm.: discovery and structural assignment
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.11.011openalex-snapshot
Asymmetric synthesis of furofurans
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154309openalex-snapshot
Progress on total synthesis and their divergent transformations of aryltetrahydrofuran-type lignans
inferred← citeshttps://doi.org/10.1016/j.toxrep.2022.05.019openalex-snapshot
Effects of dibenzylbutyrolactone lignans arctigenin and trachelogenin on the motility of isolated rat ileum
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