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Antidepressant Abietane Diterpenoids from Chinese Eaglewood
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-9422(93)85039-topenalex-snapshot
Fragrant sesquiterpenes from agarwood
inferredcites →https://doi.org/10.1016/j.jep.2008.02.005openalex-snapshot
Antinociceptive and anti-inflammatory activities of Aquilaria sinensis (Lour.) Gilg. Leaves extract
inferredcites →https://doi.org/10.1016/j.phytochem.2010.06.008openalex-snapshot
Diterpenoids from Pinus massoniana resin and their cytotoxicity against A431 and A549 cells
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.017openalex-snapshot
2-(2-Phenylethyl)chromones from Chinese eaglewood
inferredcites →https://doi.org/10.1016/j.tet.2008.02.069openalex-snapshot
Abiesanordines A–N: fourteen new norditerpenes from Abies georgei
inferredcites →https://doi.org/10.1016/j.tetlet.2005.04.072openalex-snapshot
Three novel diepoxy tetrahydrochromones from agarwood artificially produced by intentional wounding
inferredcites →https://doi.org/10.1016/s0031-9422(00)83839-xopenalex-snapshot
Agarol, a new sesquiterpene from Aquilaria agallocha
inferredcites →https://doi.org/10.1016/s0040-4020(01)88015-7openalex-snapshot
Further acidic constituents and neutral components of pinus massoniana Resin
inferredcites →https://doi.org/10.1016/s0040-4039(01)95098-1openalex-snapshot
The structure of agarotetrol, a novel highly oxygenated chromone from agarwood(jinko)
inferredcites →https://doi.org/10.1021/np0004505openalex-snapshot
Diterpenoids from the Leaves of Juniperus chinensis var. kaizuka
inferredcites →https://doi.org/10.1021/np010656lopenalex-snapshot
Oxidation Products of Abietic Acid and Its Methyl Ester
inferredcites →https://doi.org/10.1021/np50017a010openalex-snapshot
Plant Anticancer Agents. XIX. Constituents of Aquilaria malaccensis
inferredcites →https://doi.org/10.1021/np50048a024openalex-snapshot
A New and a Known Derivatives of 2-(2-Phenylethyl) Chromone from a Kind of Agarwood ("Kanankoh," in Japanese) Originating from Aquilaria agallocha
inferredcites →https://doi.org/10.1055/s-2006-957784openalex-snapshot
Effect of Jinkoh-eremol and Agarospirol from Agarwood on the Central Nervous System in Mice
inferredcites →https://doi.org/10.1080/10286020903508424openalex-snapshot
Two new 2-(2-phenylethyl)chromones from Chinese eaglewood
inferredcites →https://doi.org/10.1139/v99-218openalex-snapshot
New abietane diterpenoids from the cones of Larix kaempferi
inferredcites →https://doi.org/10.1248/cpb.50.419openalex-snapshot
Six New 2-(2-Phenylethyl)chromones from Agarwood.
inferredcites →https://doi.org/10.1248/cpb.51.560openalex-snapshot
Four New 2-(2-Phenylethyl)chromone Derivatives from Withered Wood of Aquilaria sinensis
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.2020.112554zenodo-depositor-declared
Neuroprotective compounds from the resinous heartwood of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1002/cbdv.201600091openalex-snapshot
Four New Diterpenoids from the Roots of Euphorbia pekinensis
inferred← citeshttps://doi.org/10.1002/ejoc.201402406openalex-snapshot
Merrilliadione – a Rare Isopropyl (13→11)‐abeo‐9,11‐seco Abietane Diterpene from Illicium merrillianum
inferred← citeshttps://doi.org/10.1002/slct.201701477openalex-snapshot
Regioselective Benzylic Oxidation of Aromatic Abietanes: Application to the Semisynthesis of the Naturally Occurring Picealactones A, B and C
inferred← citeshttps://doi.org/10.1007/978-3-030-03589-1_10openalex-snapshot
Endophytic Fungi: The Desired Biostimulants for Essential Oil Production
inferred← citeshttps://doi.org/10.1007/978-981-10-0833-7_4openalex-snapshot
Development of Agarwood Induction Technology Using Endophytic Fungi
inferred← citeshttps://doi.org/10.1007/s11427-019-9587-yopenalex-snapshot
Nature brings new avenues to the therapy of central nervous system diseases—An overview of possible treatments derived from natural products
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104413openalex-snapshot
Aquilaria sinensis (Lour.) Spreng: Phytochemical review and Chemotaxonomic values
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.108121openalex-snapshot
Organocatalytic enantioselective construction of bicyclic γ-butrolactones
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.01.010openalex-snapshot
Aquilariaenes A-H, eight new diterpenoids from Chinese eaglewood
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106143openalex-snapshot
Four new guaiane sesquiterpenes from Agarwood of Aquilaria sinensis and their biological activity toward renal fibrosis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121727openalex-snapshot
Optimizing pretreatment methods for agarwood (Aquilaria sinensis) essential oil: A comparative analysis of yield, physicochemical properties, and bioactivities
inferred← citeshttps://doi.org/10.1016/j.jas.2014.10.008openalex-snapshot
Use of Zanzibar copal (Hymenaea verrucosa Gaertn.) as incense at Unguja Ukuu, Tanzania in the 7–8th century CE: chemical insights into trade and Indian Ocean interactions
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.07.006openalex-snapshot
The protective effects of Aquilariae Lignum Resinatum extract on 5-Fuorouracil-induced intestinal mucositis in mice
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.07.003openalex-snapshot
Chemical constituents of Abies nukiangensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.10.008openalex-snapshot
Diterpenoids from Croton crassifolius include a novel skeleton possibly generated via an intramolecular [2+2]-photocycloaddition reaction
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113360openalex-snapshot
Diterpenes from Pinus kesiya var. langbianensis (A.Chev.) Gaussen ex Bui (Pinaceae) and their protective effects in LPS-treated BEAS-2B cells
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.011openalex-snapshot
Microbial transformations of buagarofuran, an anti-anxietic agent
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.030openalex-snapshot
Holophyllin A, a rearranged abietane-type diterpenoid from the trunk of Abies holophylla
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01292openalex-snapshot
Diterpenoids with Aromatase Inhibitory Activity from the Rhizomes of Kaempferia elegans
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00018openalex-snapshot
Bioactive Diterpenoids from the Leaves of Callicarpa macrophylla
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00462openalex-snapshot
Aquilanols A and B, Macrocyclic Humulene-Type Sesquiterpenoids from the Agarwood of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00266openalex-snapshot
A Highly Rearranged Nor-Abietane Diterpenoid with an Unusual 6/6/6/5/4 Pentacyclic System and Three Other Diterpenoids from Lycopus lucidus var. hirtus and Antineuroinflammatory Activities
inferred← citeshttps://doi.org/10.1021/acscatal.3c05918openalex-snapshot
From Functional Plasticity of Two Diterpene Synthases (IrTPS2/IrKSL3a) to Enzyme Evolution
inferred← citeshttps://doi.org/10.1021/acsomega.8b01401openalex-snapshot
Catalytic, Tunable, One-Step Bismuth(III) Triflate Reaction with Alcohols: Dehydration Versus Dimerization
inferred← citeshttps://doi.org/10.1021/ol403289yopenalex-snapshot
Synthesis of a Dicyano Abietane, a Key Intermediate for the Anti-inflammatory Agent TBE-31
inferred← citeshttps://doi.org/10.1039/c4np00108gopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c4np00110aopenalex-snapshot
Aromatic abietane diterpenoids: their biological activity and synthesis
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1080/10286020.2022.2097078openalex-snapshot
Chemical constituents from Abies chensiensis and their antifungal activity
inferred← citeshttps://doi.org/10.1080/10412905.2024.2447706openalex-snapshot
Essential oil from Aquilaria spp. (agarwood): a comprehensive review on the impact of extraction methods on yield, chemical composition, and biological activities
inferred← citeshttps://doi.org/10.1080/14756366.2019.1576657openalex-snapshot
Sesquiterpenoids and 2-(2-phenylethyl)chromones respectively acting as α-glucosidase and tyrosinase inhibitors from agarwood of an Aquilaria plant
inferred← citeshttps://doi.org/10.1080/14786419.2013.825915openalex-snapshot
Three new diterpenoids from the resin ofLiquidambar formosana
inferred← citeshttps://doi.org/10.1080/14786419.2014.942662openalex-snapshot
Microphynolides A and B, new spiro-γ-lactone glycosides fromThymelaea microphylla
inferred← citeshttps://doi.org/10.1088/1755-1315/54/1/012062openalex-snapshot
Agarwood-planted tree inventory in Indonesia
inferred← citeshttps://doi.org/10.1093/jimb/kuaf003openalex-snapshot
Biocatalytic diversification of abietic acid in Streptomyces
inferred← citeshttps://doi.org/10.2139/ssrn.4868523openalex-snapshot
Five New Guaiacol Sesquiterpenes from Agarwood of Aquilaria Sinensis and Their Biological Activity Toward Renal Fibrosis
inferred← citeshttps://doi.org/10.2174/1570180820666230726111321openalex-snapshot
In silico Pharmacodynamics, Antineoplastic Activity and Molecular Docking of two Phytochemicals Isolated from Thymelaea microphylla
inferred← citeshttps://doi.org/10.2174/1570193x14666170721143041openalex-snapshot
Review: Secondary Metabolites of Aquilaria, a Thymelaeaceae Genus
inferred← citeshttps://doi.org/10.3184/174751917x15021050367558openalex-snapshot
Pseudo-Natural Products, Some Artefacts Formed during the Isolation of Terpenoids
inferred← citeshttps://doi.org/10.3390/ijms17030398openalex-snapshot
Antiallergic Phorbol Ester from the Seeds of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.3390/ijms19113468openalex-snapshot
Agarwood Essential Oil Ameliorates Restrain Stress-Induced Anxiety and Depression by Inhibiting HPA Axis Hyperactivity
inferred← citeshttps://doi.org/10.3390/molecules21030281openalex-snapshot
Three New Sesquiterpenoids and One New Sesquiterpenoid Derivative from Chinese Eaglewood
inferred← citeshttps://doi.org/10.3390/molecules23020342openalex-snapshot
Chemical Constituents and Pharmacological Activity of Agarwood and Aquilaria Plants
inferred← citeshttps://doi.org/10.3390/molecules26247708openalex-snapshot
Aquilaria Species (Thymelaeaceae) Distribution, Volatile and Non-Volatile Phytochemicals, Pharmacological Uses, Agarwood Grading System, and Induction Methods
inferred← citeshttps://doi.org/10.3390/molecules27113386openalex-snapshot
Agarwood—The Fragrant Molecules of a Wounded Tree
inferred← citeshttps://doi.org/10.3390/molecules29020468openalex-snapshot
Solid-Phase Microextraction/Gas Chromatography–Time-of-Flight Mass Spectrometry Approach Combined with Network Pharmacology Analysis to Evaluate the Quality of Agarwood from Different Regions against Anxiety Disorder
inferred← citeshttps://doi.org/10.3892/br.2023.1598openalex-snapshot
Agarwood essential oil inhalation exerts antianxiety and antidepressant effects via the regulation of Glu/GABA system homeostasis
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