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Bi-linderone, a Highly Modified Methyl-linderone Dimer from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity in Vitro
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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.200890223openalex-snapshot
Antimycobacterial Butanolides from the Root of Lindera akoensis
inferredcites →https://doi.org/10.1016/j.antiviral.2005.02.007openalex-snapshot
Identification of natural compounds with antiviral activities against SARS-associated coronavirus
inferredcites →https://doi.org/10.1016/j.fitote.2008.09.009openalex-snapshot
Sesquiterpene lactones from Carpesium abrotanoides
inferredcites →https://doi.org/10.1016/j.lfs.2005.04.018openalex-snapshot
Water extract of the root of Lindera strychnifolia slows down the progression of diabetic nephropathy in db/db mice
inferredcites →https://doi.org/10.1016/j.phytochem.2009.03.007openalex-snapshot
Alstonic acids A and B, unusual 2,3-secofernane triterpenoids from Alstonia scholaris
inferredcites →https://doi.org/10.1016/j.tetlet.2005.10.051openalex-snapshot
New sesquiterpene lactones from water extract of the root of Lindera strychnifolia with cytotoxicity against the human small cell lung cancer cell, SBC-3
inferredcites →https://doi.org/10.1016/s0031-9422(97)00947-3openalex-snapshot
A dihydrochalcone from Lindera lucida
inferredcites →https://doi.org/10.1021/np50036a043openalex-snapshot
Alkaloids From Lindera strychnifolia
inferredcites →https://doi.org/10.1021/np900354qopenalex-snapshot
Sesquiterpene Lactones from the Root Tubers of Lindera aggregata
inferredcites →https://doi.org/10.1021/np900449ropenalex-snapshot
ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound
inferredcites →https://doi.org/10.1039/jr9620004338openalex-snapshot
843. The structure of linderone and methyl-linderone
inferredcites →https://doi.org/10.1080/10286020903048975openalex-snapshot
New geranyloxycoumarins fromToddalia asiatica
inferredcites →https://doi.org/10.1142/s0192415x04002223openalex-snapshot
Lindera strychnifolia is Protective Against Post-ischemic Myocardial Dysfunction Through Scavenging Hydroxyl Radicals and Opening the Mitochondrial K ATP Channels in Isolated Rat Hearts
inferredcites →https://doi.org/10.1248/cpb.48.614openalex-snapshot
New Cytotoxic Butanolides from Lindera obtusiloba BLUME.
inferredcites →https://doi.org/10.1248/cpb.56.864openalex-snapshot
Sulfonated Guaianolides from Saussurea lappa
inferredcites →https://doi.org/10.1248/cpb.57.525openalex-snapshot
New Terpenoids from Isodon sculponeata
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112924zenodo-depositor-declared
Linderanoids A–O, dimeric sesquiterpenoids from the roots of Lindera aggregata (Sims) Kosterm
inferred← citeshttps://doi.org/10.1002/ajoc.201200184openalex-snapshot
Concise Synthesis of Linderaspirone A and Bi‐linderone
inferred← citeshttps://doi.org/10.1002/chin.201038219openalex-snapshot
ChemInform Abstract: Bi‐linderone (I), a Highly Modified Methyl‐linderone Dimer from Lindera aggregata with Activity Toward Improvement of Insulin Sensitivity in vitro
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_13openalex-snapshot
Other Novel Skeletal Plant Natural Products
inferred← citeshttps://doi.org/10.1007/s11101-015-9432-2openalex-snapshot
The genus Lindera: a source of structurally diverse molecules having pharmacological significance
inferred← citeshttps://doi.org/10.1007/s13659-015-0078-yopenalex-snapshot
Pterocarpadiols A–D, Rare 6a,11b-Dihydroxypterocarpans from Derris robusta
inferred← citeshttps://doi.org/10.1007/s13659-016-0090-xopenalex-snapshot
Derrisisoflavones H–K and One Isoflavan Derivative from Derris robusta
inferred← citeshttps://doi.org/10.1016/b978-0-08-102822-3.00035-3openalex-snapshot
Linderaspirone A and Bi-linderone
inferred← citeshttps://doi.org/10.1016/b978-0-443-27482-4.00012-5openalex-snapshot
Advances in ultrasound-assisted synthesis of bioactive spiro compounds and naturally occurring spiro compounds: A clean and convenient approach
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.11.027openalex-snapshot
Isolinderalactone regulates the BCL-2/caspase-3/PARP pathway and suppresses tumor growth in a human glioblastoma multiforme xenograft mouse model
inferred← citeshttps://doi.org/10.1016/j.jep.2023.116954openalex-snapshot
Traditional uses, phytochemistry, pharmacology, processing methods and quality control of Lindera aggregata (Sims) Kosterm: A critical review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.02.008openalex-snapshot
Chlorantholides A–F, eudesmane-type sesquiterpene lactones from Chloranthus elatior
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.07.005openalex-snapshot
Hybridaphniphyllines A and B, Daphniphyllum alkaloid and iridoid hybrids suggestive of Diels–Alder cycloaddition in Daphniphyllum longeracemosum
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.2024.114150openalex-snapshot
Highly oxidized guaiane 12(8),15(6)-dilactones with neuroprotective activities from the roots of Lindera aggregata (Sims) Kosterm
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.03.081openalex-snapshot
One-step biomimetic synthesis of (±)-linderaspirone A and (±)-bi-linderone
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01768openalex-snapshot
Domino Michael–Michael and Aldol–Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00522openalex-snapshot
Linderalides A–D, Disesquiterpenoid–Geranylbenzofuranone Conjugates from Lindera aggregata
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02166openalex-snapshot
Aggreganoids A–F, Carbon-Bridged Sesquiterpenoid Dimers and Trimers from Lindera aggregata
inferred← citeshttps://doi.org/10.1021/ol1011289openalex-snapshot
A Pair of Windmill-Shaped Enantiomers from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity
inferred← citeshttps://doi.org/10.1021/ol200418eopenalex-snapshot
Biomimetic Total Syntheses of Linderaspirone A and Bi-linderone and Revisions of Their Biosynthetic Pathways
inferred← citeshttps://doi.org/10.1039/c5ob01524copenalex-snapshot
Total syntheses of natural products containing spirocarbocycles
inferred← citeshttps://doi.org/10.1039/c8ra03094dopenalex-snapshot
Lindera cyclopentenedione intermediates from the roots of Lindera aggregata
inferred← citeshttps://doi.org/10.1055/a-2021-7993openalex-snapshot
Investigations on Biomimetic Dimerization in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1071/ch14655openalex-snapshot
A Simple, One-Pot Synthesis of Trans-Substituted Spiro [5,5] undecane-1,5,9-triones with Aromatic Aldehydes and Meldrum’s Acid as the Starting Materials
inferred← citeshttps://doi.org/10.1080/14786419.2021.1939332openalex-snapshot
Two new sesquiterpenoid lactone derivatives from Lindera aggregata
inferred← citeshttps://doi.org/10.1248/cpb.58.1267openalex-snapshot
Scutebarbatines W-Z, New neo-Clerodane Diterpenoids from Scutellaria barbata and Structure Revision of a Series of 13-Spiro neo-Clerodanes
inferred← citeshttps://doi.org/10.1248/cpb.59.484openalex-snapshot
Pterisolic Acids A-F, New ent-Kaurane Diterpenoids from the Fern Pteris semipinnata
inferred← citeshttps://doi.org/10.3389/fnut.2022.1071276openalex-snapshot
A review on the chemical constituents and pharmacological efficacies of Lindera aggregata (Sims) Kosterm
inferred← citeshttps://doi.org/10.3390/ijms21207530openalex-snapshot
Isolinderalactone Induces Cell Death via Mitochondrial Superoxide- and STAT3-Mediated Pathways in Human Ovarian Cancer Cells
inferred← citeshttps://doi.org/10.3390/ijms23137122openalex-snapshot
Effects of Compounds Isolated from Lindera erythrocarpa on Anti-Inflammatory and Anti-Neuroinflammatory Action in BV2 Microglia and RAW264.7 Macrophage
inferred← citeshttps://doi.org/10.3390/molecules28124590openalex-snapshot
New Phenolic Dimers from Plant Paeonia suffruticosa and Their Cytotoxicity and NO Production Inhibition
inferred← citeshttps://doi.org/10.37360/blacpma.20.19.6.37openalex-snapshot
Lindera aggregata (Sims) Kosterm: Review on phytochemistry and biological activities
inferred← citeshttps://doi.org/10.3892/ol.2022.13448openalex-snapshot
Isolinderalactone inhibits glioblastoma cell supernatant‑induced angiogenesis
inferred← citeshttps://doi.org/10.3892/or.2015.4503openalex-snapshot
Isolinderalactone enhances the inhibition of SOCS3 on STAT3 activity by decreasing miR-30c in breast cancer
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