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Diterpenoids and Diacetylenes from the Roots of Aralia cordata with Inhibitory Effects on Nitric Oxide Production
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf02969263openalex-snapshot
Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata
inferredcites →https://doi.org/10.1007/bf02975131openalex-snapshot
Inhibitory Constituents against Cyclooxygenases fromAralia cordata Thunb
inferredcites →https://doi.org/10.1007/bf02976683openalex-snapshot
Inhibitory effect of kaurane type diterpenoids fromAcanthopanax koreanum on TNF-α secretion from trypsin-stimulated HMC-1 cells
inferredcites →https://doi.org/10.1007/bf02977364openalex-snapshot
Cytotoxic and DNA topoisomerases I and II inhibitory constituents from the roots ofAralia cordata
inferredcites →https://doi.org/10.1007/s12272-009-2009-0openalex-snapshot
Cholinesterase and BACE1 inhibitory diterpenoids from Aralia cordata
inferredcites →https://doi.org/10.1016/j.bioorg.2018.05.022openalex-snapshot
Nitric oxide inhibitory constituents from Siegesbeckia pubescens
inferredcites →https://doi.org/10.1016/j.bmc.2006.09.048openalex-snapshot
Synthesis and trypanocidal activity of ent-kaurane glycosides
inferredcites →https://doi.org/10.1016/j.pupt.2009.12.004openalex-snapshot
Inhibitory effects of diterpene acids from root of Aralia cordata on IgE-mediated asthma in guinea pigs
inferredcites →https://doi.org/10.1016/j.tet.2014.05.006openalex-snapshot
Diterpenes and sesquiterpenes with anti-Coxsackie virus B3 activity from the stems of Illicium jiadifengpi
inferredcites →https://doi.org/10.1016/s0031-9422(00)80485-9openalex-snapshot
Ent-pimaranes, ent-kauranes, Heliangolides and other Constituents of three Helianthus species
inferredcites →https://doi.org/10.1016/s0031-9422(00)84785-8openalex-snapshot
Diterpenoids and a sesquiterpene lactone from viguiera ladibractate
inferredcites →https://doi.org/10.1016/s0031-9422(00)97022-5openalex-snapshot
Kaurane and trachylobane diterpenes from Xylopia aethiopica
inferredcites →https://doi.org/10.1016/s0040-4039(00)77990-1openalex-snapshot
Structures of stevia diterpene-glucosides : Application of 13C NMR
inferredcites →https://doi.org/10.1016/s0040-4039(01)89652-0openalex-snapshot
The occurrence of (−)pimarane-type diterpene in aralia cordata thunb
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00150openalex-snapshot
ent-Strobane andent-Pimarane Diterpenoids fromSiegesbeckia pubescens
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00691openalex-snapshot
Polyacetylenes from Oplopanax horridus and Panax ginseng: Relationship between Structure and PPARγ Activation
inferredcites →https://doi.org/10.1021/np0104018openalex-snapshot
Gymnasterkoreaynes A−F, Cytotoxic Polyacetylenes from Gymnaster koraiensis
inferredcites →https://doi.org/10.1021/np0202475openalex-snapshot
New Chemical Constituents of Euphorbia q uinquecostata and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
inferredcites →https://doi.org/10.1021/np500125xopenalex-snapshot
Anti-inflammatory Diterpenoids from the Root Bark of Acanthopanax gracilistylus
inferredcites →https://doi.org/10.1021/np50060a005openalex-snapshot
Pimaradiene Diterpenes from Acanthopanax koreanum
inferredcites →https://doi.org/10.1021/np800581sopenalex-snapshot
Antibacterial Diterpenes from Plectranthus ernstii
inferredcites →https://doi.org/10.1021/np960224oopenalex-snapshot
Cytotoxic Falcarinol Oxylipins from Dendropanax arboreus
inferredcites →https://doi.org/10.1021/np980418zopenalex-snapshot
Stereoselective Total Synthesis of (3R,8S)-Falcarindiol, a Common Polyacetylenic Compound from Umbellifers
inferredcites →https://doi.org/10.1039/c6ra08986kopenalex-snapshot
Diterpenoids from the shed trunk barks of the endangered plant Pinus dabeshanensis and their PTP1B inhibitory effects
inferredcites →https://doi.org/10.1055/s-0042-104349openalex-snapshot
Cytotoxic Diterpenoids from the Roots of Aralia melanocarpa
inferredcites →https://doi.org/10.1055/s-2001-16491openalex-snapshot
Two New Bislabdane-Type Diterpenoids and Three New Diterpenoids from the Roots of Cunninghamia lanceolata
inferredcites →https://doi.org/10.1080/10286020.2019.1567503openalex-snapshot
Three new diterpenoids from Aralia dumetorum
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1107/s2053229614024929openalex-snapshot
PLATON SQUEEZE: a tool for the calculation of the disordered solvent contribution to the calculated structure factors
inferredcites →https://doi.org/10.1248/cpb.22.1629openalex-snapshot
Minor Diterpenes of Aralia cordata THUNB. : 17-Hydroxy-ent-kaur-15-en-19-oic Acid and Grandifloric Acid
inferredcites →https://doi.org/10.2174/1568026615666141208110021openalex-snapshot
The Medicinal Chemistry of Genus Aralia
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.2022.113301zenodo-depositor-declared
Anti-inflammatory withanolides from the aerial parts of Physalis minima
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113319zenodo-depositor-declared
Polyacetylenes from the roots of Cirsium japonicum var. ussuriense
inferred← citeshttps://doi.org/10.1002/cjoc.202200220openalex-snapshot
Isosteroidal Alkaloids from Fritillaria verticillata Willd. and Their NMR Spectroscopic Characteristics
inferred← citeshttps://doi.org/10.1007/s00226-024-01566-xopenalex-snapshot
Extraction and investigation of the lipophilic fraction from Norway spruce (Picea abies) and Scots pine (Pinus sylvestris) forestry side-stream biomass
inferred← citeshttps://doi.org/10.1007/s11101-023-09887-8openalex-snapshot
The standardization of officinal medicinal plants used in the Eurasian Economic Union: comparison with other pharmacopoeias
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114671openalex-snapshot
Traditional uses, phytochemistry, pharmacology, toxicity and quality control of medicinal genus Aralia: A review
inferred← citeshttps://doi.org/10.1016/j.joim.2023.06.006openalex-snapshot
Phytochemical interventions for post-traumatic stress disorder: A cluster co-occurrence network analysis using CiteSpace
inferred← citeshttps://doi.org/10.1039/d3ob00575eopenalex-snapshot
Asymmetric syntheses of ent -pimarane diterpenoids
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10998138/v1openalex-snapshot
Chromosome-level genome assembly of Aralia cordata unveils evolution history and genomic landscape diversification in Aralia-Panax
inferred← citeshttps://doi.org/10.3389/fntpr.2022.1086897openalex-snapshot
Computational methods and points for attention in absolute configuration determination
inferred← citeshttps://doi.org/10.3390/antiox13080950openalex-snapshot
Phytochemical and Functional Diversity of Enzyme-Assisted Extracts from Hippophae rhamnoides L., Aralia cordata Thunb., and Cannabis sativa L.
inferred← citeshttps://doi.org/10.3390/plants11131704openalex-snapshot
Aralia cordata Thunb. as a Source of Bioactive Compounds: Phytochemical Composition and Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/su16062582openalex-snapshot
Utilization of Inedible Parts of Aralia cordata with High-Content Chlorogenic Acid Cultivated in Tokyo
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