On the public citation graph

A Pair of Windmill-Shaped Enantiomers from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity

https://doi.org/10.1021/ol1011289
0 signed · 66 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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/10.1002/ejoc.200900422openalex-snapshot
Assignment of the Absolute Configuration of Concentricolide – Absolute Configuration Determination of Its Bioactive Analogs Using DFT Methods
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.cmet.2007.08.014openalex-snapshot
SIRT1 Improves Insulin Sensitivity under Insulin-Resistant Conditions by Repressing PTP1B
inferredcites →https://doi.org/10.1016/j.cplett.2004.11.082openalex-snapshot
Coupled cluster calculations of the optical rotation of S-propylene oxide in gas phase and solution
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.tetasy.2008.02.030openalex-snapshot
Study of syntheses and specific rotations of (S)-3-phenylhexan-3-ol and its derivatives
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/10.1021/ja050483copenalex-snapshot
Determination of Molecular Structure in Solution Using Vibrational Circular Dichroism Spectroscopy: the Supramolecular Tetramer of S -2,2‘-Dimethyl-Biphenyl-6,6‘-Dicarboxylic Acid
inferredcites →https://doi.org/10.1021/jp040724nopenalex-snapshot
Conformational Effects on Optical Rotation. 2-Substituted Butanes
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/10.1021/ol1007247openalex-snapshot
Bi-linderone, a Highly Modified Methyl-linderone Dimer from Lindera aggregata with Activity toward Improvement of Insulin Sensitivity in Vitro
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/adsc.201100592openalex-snapshot
Chiral Biscarboline N,N′‐Dioxide Derivatives: Highly Enantioselective Addition of Allyltrichlorosilane to Aldehydes
inferred← citeshttps://doi.org/10.1002/ajoc.201200184openalex-snapshot
Concise Synthesis of Linderaspirone A and Bi‐linderone
inferred← citeshttps://doi.org/10.1007/978-3-319-67062-1_11openalex-snapshot
Radix Linderae – Wuyao
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/s13659-013-0053-4openalex-snapshot
Isoprenylated flavonoids and clerodane diterpenoids from Dodonaea viscosa
inferred← citeshttps://doi.org/10.1007/s13659-015-0076-0openalex-snapshot
Lanostane-Type Triterpenoids from Scilla scilloides and Structure Revision of Drimiopsin D
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.bmcl.2020.127224openalex-snapshot
Anti-inflammatory principles from Lindera aggregata
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.fitote.2019.104285openalex-snapshot
The NCI library of traditional Chinese medicinal plant extracts – Preliminary assessment of the NCI-60 activity and chemical profiling of selected species
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.jff.2024.106188openalex-snapshot
The sesquiterpene lactone-enriched extract from Linderae Radix ameliorated high glucose-induced renal tubular epithelial injury via mediating PPARγ/Nrf2 pathway
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.phytochem.2026.114881openalex-snapshot
Structurally diverse sesquiterpenoids from the roots of Lindera aggregata and their anti-necroptosis activities
inferred← citeshttps://doi.org/10.1016/j.prmcm.2024.100387openalex-snapshot
A brief history: Traditional Chinese medicinal system
inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.082openalex-snapshot
Determining the absolute configuration of benzopyrenomycin by optical rotation, electronic circular dichroism, and population analysis of different conformations via DFT methods and experiments
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.032openalex-snapshot
Discussion of absolute configuration for bioactive Griseusins by comparing computed optical rotations and electronic circular dichroism with the experimental results
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/10.1016/j.tetlet.2013.03.125openalex-snapshot
Two pairs of new benzofuran enantiomers with unusual skeletons from Eupatorium chinense
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.06.097openalex-snapshot
Flueggedine, a novel axisymmetric indolizidine alkaloid dimer from Flueggea virosa
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.088openalex-snapshot
A pair of unprecedented cyclohexylethanoid enantiomers containing unusual trioxabicyclo[4.2.1]nonane ring from Clerodendrum bungei
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/acsomega.0c06349openalex-snapshot
Linderaggrenolides A–N, Oxygen-Conjugated Sesquiterpenoid Dimers from the Roots of Lindera aggregata
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/10.1080/10286020.2011.565747openalex-snapshot
A novel phenolic compound from Pinus yunnanensis
inferred← citeshttps://doi.org/10.1080/10286020.2014.965161openalex-snapshot
A new phenylpropanoid and a new isoflavone glycoside from Shenqi Fuzheng Injection
inferred← citeshttps://doi.org/10.1080/10286020.2017.1307186openalex-snapshot
A new α-pyrone from the deep-sea actinomycete Nocardiopsis dassonvillei subsp. dassonvillei DSM 43111(T)
inferred← citeshttps://doi.org/10.1080/14786419.2021.1939332openalex-snapshot
Two new sesquiterpenoid lactone derivatives from Lindera aggregata
inferred← citeshttps://doi.org/10.1177/1934578x1200701010openalex-snapshot
In Silico Prediction of the Cosmetic Whitening Effects of Naturally Occurring Lead Compounds
inferred← citeshttps://doi.org/10.1177/1934578x1501001229openalex-snapshot
New Benzenoids from the Roots of Lindera aggregata
inferred← citeshttps://doi.org/10.1186/s13020-017-0145-xopenalex-snapshot
A network pharmacology-based strategy deciphers the underlying molecular mechanisms of Qixuehe Capsule in the treatment of menstrual disorders
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/10.3389/fphar.2021.627920openalex-snapshot
Linderae Radix Ethanol Extract Alleviates Diet-Induced Hyperlipidemia by Regulating Bile Acid Metabolism Through gut Microbiota
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/10.3892/or.2015.4503openalex-snapshot
Isolinderalactone enhances the inhibition of SOCS3 on STAT3 activity by decreasing miR-30c in breast cancer
inferred← citeshttps://doi.org/10.3945/an.111.000703openalex-snapshot
Research Advances at the Institute for Nutritional Sciences at Shanghai, China
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.