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Nudibaccatumone, a Trimer Comprising a Phenylpropanoid and Two Sesquiterpene Moieties from Piper nudibaccatum
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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.
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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/(sici)1096-987x(19991130)20:15<1671::aid-jcc7>3.0.co;2-yopenalex-snapshot
Low-mode conformational search elucidated: Application to C39H80 and flexible docking of 9-deazaguanine inhibitors into PNP
inferredcites →https://doi.org/10.1006/abbi.1999.1122openalex-snapshot
Isolation, Characterization, and Mechanistic Studies of (−)-α-Gurjunene Synthase fromSolidago canadensis
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0031-9422(86)88017-7openalex-snapshot
Juvenile-adult chemical dimorphism in foliage of Dacrydium biforme
inferredcites →https://doi.org/10.1016/j.tet.2010.05.078openalex-snapshot
Hypervalent iodine-mediated oxygenative phenol dearomatization reactions
inferredcites →https://doi.org/10.1016/s0031-9422(00)90406-0openalex-snapshot
Cadinane-type sesquiterpenoids from the liverwort Scapania undulata
inferredcites →https://doi.org/10.1016/s0031-9422(97)00328-2openalex-snapshot
Phytochemistry of the genus Piper
inferredcites →https://doi.org/10.1016/s0040-4039(00)79578-5openalex-snapshot
Macrocarpals: HIV-RTase inhibitors of Eucalyptus globulus
inferredcites →https://doi.org/10.1021/jp003919dopenalex-snapshot
Evaluation and Reparametrization of the OPLS-AA Force Field for Proteins via Comparison with Accurate Quantum Chemical Calculations on Peptides
inferredcites →https://doi.org/10.1021/jp810292nopenalex-snapshot
Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions
inferredcites →https://doi.org/10.1021/np100606uopenalex-snapshot
Cytotoxic Amide Alkaloids from Piper boehmeriaefolium
inferredcites →https://doi.org/10.1021/ol103079vopenalex-snapshot
How Many Secondary Carbocations Are Involved in the Biosynthesis of Avermitilol?
inferredcites →https://doi.org/10.1021/tx00039a024openalex-snapshot
Evidence That 4-Allyl-o-quinones Spontaneously Rearrange to Their More Electrophilic Quinone Methides: Potential Bioactivation Mechanism for the Hepatocarcinogen Safrole
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1351/pac200779040529openalex-snapshot
Chemistry and evolution of the Piperaceae
inferredcites →https://doi.org/10.1590/s0103-50532003000500020openalex-snapshot
Antifungal aromadendrane sesquiterpenoids from the leaves of Xylopia brasiliensis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.316.2.8zenodo-depositor-declared
Piper magen (Piperaceae), a new species from Yunnan, China
inferred← citeshttps://doi.org/10.1002/cbdv.202100458openalex-snapshot
Neolignans and Sesquiterpenoid from Piper yunnanense
inferred← citeshttps://doi.org/10.1002/pfm2.70007openalex-snapshot
Orthoquinone, Cyclic, and Acyclic α‐Diketone Natural Products: From Food Applications to Pharmacotherapy
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_8openalex-snapshot
Classification of Diverse Novel Meroterpenoids
inferred← citeshttps://doi.org/10.1007/s11101-020-09698-1openalex-snapshot
Natural disesquiterpenoids: an overview of their chemical structures, pharmacological activities, and biosynthetic pathways
inferred← citeshttps://doi.org/10.1007/s13659-013-0073-0openalex-snapshot
New amide alkaloids from Piper longum fruits
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.08.063openalex-snapshot
Multidrug resistance-selective antiproliferative activity of Piper amide alkaloids and synthetic analogues
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115014openalex-snapshot
Artemselenolides I–N, sesquiterpenoid trimers from Artemisia selengensis with antihepatoma activity – structural elucidation, molecular docking and dynamics studies
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.03.005openalex-snapshot
Xanthine oxidase inhibitors isolated from Piper nudibaccatum
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.005openalex-snapshot
Isolation and synthesis of two hydroxychavicol heterodimers from Piper nudibaccatum
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00522openalex-snapshot
Linderalides A–D, Disesquiterpenoid–Geranylbenzofuranone Conjugates from Lindera aggregata
inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferred← citeshttps://doi.org/10.1039/d5np00065copenalex-snapshot
Trimeric natural products: structural diversity, biosynthesis, bioactivities and chemical synthesis
inferred← citeshttps://doi.org/10.1177/1934578x1601100948openalex-snapshot
A Survey of the Chemical Compounds of Piper spp. (Piperaceae) and Their Biological Activities
inferred← citeshttps://doi.org/10.4103/2225-4110.124811openalex-snapshot
Anticancer Principles from Medicinal Piper (胡椒 Hú Jiāo) Plants
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