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Dibenzylbutyrolactone and Dibenzylbutanediol Lignans from Peperomia duclouxii

https://doi.org/10.1021/np030247k
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What this work says

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

inferredcites →https://doi.org/10.1016/s0031-9422(00)80428-8openalex-snapshot
Biological activities of lignans
inferredcites →https://doi.org/10.1016/s0031-9422(00)84995-xopenalex-snapshot
Neolignans from Ocotea aciphylla
inferredcites →https://doi.org/10.1016/s0031-9422(00)89595-3openalex-snapshot
4-O-Demethylyatein from the branch wood ofThuja occidentalis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00932-1openalex-snapshot
A prenylated benzopyran derivative from peperomia clusiifolia
inferredcites →https://doi.org/10.1016/s0031-9422(97)01050-9openalex-snapshot
Phenolic compounds from peperomia obtusifolia
inferredcites →https://doi.org/10.1016/s0031-9422(98)00393-8openalex-snapshot
Two secolignans from Peperomia dindigulensis
inferredcites →https://doi.org/10.1021/np960148popenalex-snapshot
New Prenylated Quinones from Peperomia galioides
inferredcites →https://doi.org/10.1021/np990447popenalex-snapshot
Proctoriones A−C: 2-Acylcyclohexane-1,3-dione Derivatives from Peperomia proctorii

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4529481openalex-extracted
Two Novel Butyrolactone Lignan Dimers from Leaves of Chastanopsis Chinensis and Their Anti-Inflammatory Activities
inferred← citeshttps://doi.org/10.1002/ejoc.201000318openalex-snapshot
General Approach to 2,3‐Dibenzyl‐γ‐butyrolactone Lignans: Application to the Total Synthesis of (±)‐5′‐Methoxyyatein, (±)‐5′‐Methoxyclusin, and (±)‐4′‐Hydroxycubebinone
inferred← citeshttps://doi.org/10.1002/hlca.200790230openalex-snapshot
A Novel Norlignan and a Novel Phenylpropanoid from Peperomia tetraphylla
inferred← citeshttps://doi.org/10.1002/jms.4676openalex-snapshot
Top–down lignomics analysis of the French oak lignin by atmospheric pressure photoionization and electrospray ionization quadrupole time‐of‐flight tandem mass spectrometry: Identification of a novel series of lignans
inferred← citeshttps://doi.org/10.1002/ptr.4932openalex-snapshot
The Lignan (‐)‐Cubebin Inhibits Vascular Contraction and Induces Relaxation Via Nitric Oxide Activation in Isolated Rat Aorta
inferred← citeshttps://doi.org/10.1007/s11101-016-9461-5openalex-snapshot
Natural products from Peperomia: occurrence, biogenesis and bioactivity
inferred← citeshttps://doi.org/10.1007/s11418-024-01864-5openalex-snapshot
Two novel butyrolactone lignan dimers from leaves of Castanopsis chinensis and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.12.012openalex-snapshot
Unusual chromenes from Peperomia blanda
inferred← citeshttps://doi.org/10.1016/j.phytochem.2006.01.019openalex-snapshot
Configurational analysis of cubebins and bicubebin from Aristolochia lagesiana and Aristolochia pubescens
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.11.008openalex-snapshot
Phenylpropanoids and a diarylpentanol from Stellera chamaejasme with acetylcholinesterase inhibitory activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00300openalex-snapshot
Sumatranins A–J: Lignans with Immunosuppressive Activity from Cleistanthus sumatranus
inferred← citeshttps://doi.org/10.1021/ol302358jopenalex-snapshot
Enantioselective Route to Ketones and Lactones from Exocyclic Allylic Alcohols via Metal and Enzyme Catalysis
inferred← citeshttps://doi.org/10.1039/c2ob25109dopenalex-snapshot
VCD to determine absolute configuration of natural product molecules: secolignans from Peperomia blanda
inferred← citeshttps://doi.org/10.1080/14786410701628739openalex-snapshot
Cytotoxic activity ofIpomoea cairica
inferred← citeshttps://doi.org/10.1080/14786410802236432openalex-snapshot
A new lignan glycoside fromPeperomia duclouxii
inferred← citeshttps://doi.org/10.1080/14786419.2012.708658openalex-snapshot
Three new diarylbutane lignans from the resin ofBursera fagaroides
inferred← citeshttps://doi.org/10.1177/1934578x0600100205openalex-snapshot
Two New Dibenzylbutyrolactone Type Lignans from the Stems of Kadsura heteroclita
inferred← citeshttps://doi.org/10.1248/cpb.52.1466openalex-snapshot
Matrix Metalloproteinase-1 Inhibitor from the Stem Bark of Styrax japonica S. et Z.
inferred← citeshttps://doi.org/10.20307/nps.2025.31.4.209openalex-snapshot
Extraction, Isolation, and Structural Elucidation of Lignans from Natural Resources
inferred← citeshttps://doi.org/10.3184/030823409x12506792542747openalex-snapshot
Synthesis, anti-virus and anti-tumour activities of dibenzylbutyrolactone lignans and their analogues
inferred← citeshttps://doi.org/10.3390/m855openalex-snapshot
(S)-2-Methyl-2-(4-methylpent-3-enyl)-6-(propan-2-ylidene)-3,4,6,7-tetrahydropyrano[4,3-g]chromen-9(2H)-one
inferred← citeshttps://doi.org/10.3390/molecules24214005openalex-snapshot
Isolation, Structure Elucidation, and Antiproliferative Activity of Butanolides and Lignan Glycosides from the Fruit of Hernandia nymphaeifolia
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