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Antifungal Stilbenoids from Stemona collinsae
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Outgoing claims: the papers this work cites, builds on, or argues with.
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inferredcites →https://doi.org/10.1021/jf990509hopenalex-snapshot
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Isoprenoid-substituted phenolic compounds of moraceous plants
inferredcites →https://doi.org/10.1055/s-2006-960822openalex-snapshot
2,3-Dihydrobiflavone fromGinkgo biloba
inferredcites →https://doi.org/10.1201/9780203752647openalex-snapshot
Handbook of Phytoalexin Metabolism and Action
inferredcites →https://doi.org/10.1515/zna-1993-0705openalex-snapshot
Composite Particle Theory in Quantum Electrodynamics
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
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inferred← citeshttps://doi.org/10.1002/anie.201206233openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbdv.200490023openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11745-005-1449-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-394591-4.00001-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91097-2.00006-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chembiol.2007.05.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e07970openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e38539openalex-snapshot
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Pesticidal plants as a possible alternative to synthetic acaricides in tick control: A systematic review and meta-analysis
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The traditional uses, phytochemistry, and pharmacology of Stemona species: A review
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114633openalex-snapshot
Anti-neuroinflammatory activity of 6,7-dihydroxy-2,4-dimethoxy phenanthrene isolated from Dioscorea batatas Decne partly through suppressing the p38 MAPK/NF-κB pathway in BV2 microglial cells
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2011.04.021openalex-snapshot
Antimetastatic activity of pinosylvin, a natural stilbenoid, is associated with the suppression of matrix metalloproteinases
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.09.034openalex-snapshot
Synthesis of stemofurans C, L and T using organomanganese arene chemistry; Revised structure for stemofuran L
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Determination and assay validation of pinosylvin in rat serum: application to drug metabolism and pharmacokinetics
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2003.09.015openalex-snapshot
Dihydrophenanthrenes and other antifungal stilbenoids from Stemona cf. pierrei
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.03.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.07.012openalex-snapshot
Antibacterial stilbenoids from the roots of Stemona tuberosa
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.12.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.12.014openalex-snapshot
Prenylated arylbenzofuran derivatives from Morus mesozygia with antioxidant activity
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Aryl benzofuran derivatives from the stem bark of Calpocalyx dinklagei attenuate inflammation
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A phytochemical investigation of Stemona parviflora roots reveals several compounds with nematocidal activity
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Phenylbenzofuran-type stilbenoids from Stemona species
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Metabolites isolated from the rhizomes of Dorstenia contrajerva with anti-leishmanial activity
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Parvistemins A–D, a new type of dimeric phenylethyl benzoquinones from Stemona parviflora Wright
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inferred← citeshttps://doi.org/10.1016/s0031-9422(03)00332-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0031-9422(03)00348-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0031-9422(03)00417-5openalex-snapshot
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Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s1005-9040(07)60010-5openalex-snapshot
Rapid Identification of Bibenzyls of Stemona sessilifolia using Hyphenated LC-UV-NMR and LC-MS Methods
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inferred← citeshttps://doi.org/10.1016/s1572-5995(08)80032-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c00616openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.3c07103openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.5c05183openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00930openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00539openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.1c05450openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.2c01572openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.2c03681openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acscatal.8b01364openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsinfecdis.4c00828openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jf0205615openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo3000805openalex-snapshot
Homo- and Hetero-oxidative Coupling of Benzyl Anions
inferred← citeshttps://doi.org/10.1021/jo400984hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np0497043openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np0504154openalex-snapshot
Neuroprotective Bibenzyl Glycosides of Stemona tuberosa Roots
inferred← citeshttps://doi.org/10.1021/np070010eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np100474yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np100668sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np2004374openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np300690copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np400379uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol049564oopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol201246eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol202478uopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol202858fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-023-42500-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c005018kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2gc16457dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c2np20049jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c3cc42326copenalex-snapshot
Facile synthesis of benzofurans via copper-catalyzed aerobic oxidative cyclization of phenols and alkynes
inferred← citeshttps://doi.org/10.1039/c4ob00575aopenalex-snapshot
Palladium-catalyzed tandem reaction of 2-hydroxyarylacetonitriles with sodium sulfinates: one-pot synthesis of 2-arylbenzofurans
inferred← citeshttps://doi.org/10.1039/c4ob02691hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5ob02336jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c6qo00112bopenalex-snapshot
Hydrazone–palladium catalyzed annulation of 1-cinnamyloxy-2-ethynylbenzene derivatives
inferred← citeshttps://doi.org/10.1039/c7ra03551aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9ra10835aopenalex-snapshot
Antioxidation of 2-phenylbenzofuran derivatives: structural-electronic effects and mechanisms
inferred← citeshttps://doi.org/10.1039/d2sc06725kopenalex-snapshot
Regioselective C–H alkylation of anisoles with olefins by cationic imidazolin-2-iminato scandium( iii ) alkyl complexes
inferred← citeshttps://doi.org/10.1080/07929978.2015.1006424openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10286020500382678openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10286020600604310openalex-snapshot
Stilbenoids from Stemona sessilifolia
inferred← citeshttps://doi.org/10.1080/10286020701189286openalex-snapshot
Antibacterial constituents fromStemona sessilifolia
inferred← citeshttps://doi.org/10.1080/10286020802133555openalex-snapshot
Antifungal stilbenoids fromStemona japonica
inferred← citeshttps://doi.org/10.1080/14786419.2015.1045507openalex-snapshot
Non-alkaloids extract from Stemona sessilifolia enhances the activity of chemotherapeutic agents through P-glycoprotein-mediated multidrug-resistant cancer cells
inferred← citeshttps://doi.org/10.1080/14786419.2020.1798662openalex-snapshot
Stilbenoids from the roots of Stemona tuberosa
inferred← citeshttps://doi.org/10.1155/2022/2599689openalex-snapshot
Pharmacological Properties to Pharmacological Insight of Sesamin in Breast Cancer Treatment: A Literature-Based Review Study
inferred← citeshttps://doi.org/10.1186/s13765-019-0436-2openalex-snapshot
Anti-inflammatory and antioxidant effects of 2, 7-dihydroxy-4, 6-dimethoxy phenanthrene isolated from Dioscorea batatas Decne
inferred← citeshttps://doi.org/10.1248/bpb.29.1490openalex-snapshot
Growth Inhibition of Stilbenoids in Welwitschiaceae and Gnetaceae through Induction of Apoptosis in Human Leukemia HL60 Cells
inferred← citeshttps://doi.org/10.1248/cpb.60.270openalex-snapshot
Synthesis of 2-Phenylbenzofuran Derivatives and Selective Binding Activities on Estrogen Receptor
inferred← citeshttps://doi.org/10.1248/yakushi.128.1139openalex-snapshot
Selective Synthesis of Benzofurans and Dihydrobenzofurans via Efficient Rearrangement as Key Reaction
inferred← citeshttps://doi.org/10.20307/nps.2018.24.4.266openalex-snapshot
Five New Stilbenes from the Stem Bark ofArtocarpus communis
inferred← citeshttps://doi.org/10.2174/0118756298307930240531072440openalex-snapshot
A Comprehensive Review on History, Sources, Biosynthesis, Chemical Synthesis and Applications of Stilbenes
inferred← citeshttps://doi.org/10.3390/catal8040136openalex-snapshot
[(PhCH2O)2P(CH3)2CHNCH(CH3)2]2PdCl2/CuI as Cocatalyst for Coupling-Cyclization of 2-Iodophenol with Terminal Alkynes in Water
inferred← citeshttps://doi.org/10.3390/cimb47030204openalex-snapshot
Pinosylvin: A Multifunctional Stilbenoid with Antimicrobial, Antioxidant, and Anti-Inflammatory Potential
inferred← citeshttps://doi.org/10.3390/molecules27227676openalex-snapshot
Phenylpropanoid Derivatives from the Tuber of Asparagus cochinchinensis with Anti-Inflammatory Activities
inferred← citeshttps://doi.org/10.3390/molecules30091982openalex-snapshot
Stilbenes Against Alzheimer’s Disease: A Comprehensive Review of Preclinical Studies of Natural and Synthetic Compounds Combined with the Contributions of Developed Nanodrug Delivery Systems
inferred← citeshttps://doi.org/10.3839/jabc.2017.034openalex-snapshot
Antifungal activity of pinosylvin fromPinus densifloraon turfgrass fungal diseases
inferred← citeshttps://doi.org/10.3987/rev-08-645openalex-snapshot
Efficient Synthesis of Indoles and Benzo[b]furans via [3,3]-Sigmatropic Rearrangement of N-Trifluoroacetylenehydrazines and Enehydroxylamines
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.10.3027openalex-snapshot
Concise Synthesis of Stemofurans A, C, and Derivatives
inferred← citeshttps://doi.org/10.5012/bkcs.2011.32.2.566openalex-snapshot
Efficient Synthesis of Bibenzyl Derivatives Bearing Pyranyl Moieties: First Total Synthesis of Bauhinol D
inferred← citeshttps://doi.org/10.5012/bkcs.2012.33.7.2247openalex-snapshot
Two New Bibenzyl Glucosides from Dendrobium chrysotoxum
inferred← citeshttps://doi.org/10.5958/j.0975-4261.2.1.001openalex-snapshot
Oral absorption and antitussive activity of tuberostemonine alkaloids from the roots of Stemona tuberosa
inferred← citeshttps://doi.org/10.70675/1125fe31z1ec3z49c6zbbc7zaa4f9719f0f0openalex-snapshot
Non-covalent interactions in natural products
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