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Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their 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.
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Analysis of the polar fraction of Haitian vetiver oil
inferredcites →https://doi.org/10.1002/cbdv.200900160openalex-snapshot
Four New Sesquiterpenes from Curcuma wenyujin and Their Inhibitory Effects on Nitric‐Oxide Production
inferredcites →https://doi.org/10.1002/chir.1037openalex-snapshot
Chiroptical properties of binuclear rhodium complexes of lanostane alcohols
inferredcites →https://doi.org/10.1002/hlca.200900059openalex-snapshot
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inferredcites →https://doi.org/10.1016/0031-9422(88)83038-3openalex-snapshot
Terpenoids from Curcuma heyneana
inferredcites →https://doi.org/10.1016/0031-9422(90)83038-3openalex-snapshot
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inferredcites →https://doi.org/10.1016/0031-9422(93)85179-uopenalex-snapshot
Anti-oxidative and anti-inflammatory curcumin-related phenolics from rhizomes of Curcuma domestica
inferredcites →https://doi.org/10.1016/0031-9422(95)00425-7openalex-snapshot
Guaiane sesquiterpene lactones from Curcuma aeruginosa
inferredcites →https://doi.org/10.1016/j.bmcl.2011.07.012openalex-snapshot
Diarylheptanoids from Curcuma kwangsiensis and their inhibitory activity on nitric oxide production in lipopolysaccharide-activated macrophages
inferredcites →https://doi.org/10.1016/j.phymed.2011.06.017openalex-snapshot
Anti-tumor potential of ethanol extract of Curcuma phaeocaulis Valeton against breast cancer cells
inferredcites →https://doi.org/10.1016/j.phytochem.2011.08.004openalex-snapshot
Linderolides A–F, eudesmane-type sesquiterpene lactones and linderoline, a germacrane-type sesquiterpene from the roots of Lindera strychnifolia and their inhibitory activity on NO production in RAW 264.7 cells in vitro
inferredcites →https://doi.org/10.1016/s0040-4020(01)00828-6openalex-snapshot
Absolute stereostructure of carabrane-type sesquiterpene and vasorelaxant-active sesquiterpenes from Zedoariae Rhizoma
inferredcites →https://doi.org/10.1016/s0040-4020(01)98282-1openalex-snapshot
Circulardichroismus—VIII
inferredcites →https://doi.org/10.1016/s0891-5849(00)00294-xopenalex-snapshot
Curcumin, an antioxidant and anti-inflammatory agent, induces heme oxygenase-1 and protects endothelial cells against oxidative stress
inferredcites →https://doi.org/10.1016/s0957-4166(99)00115-9openalex-snapshot
[Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols
inferredcites →https://doi.org/10.1016/s0960-894x(98)00021-3openalex-snapshot
Inhibitory effect and action mechanism of sesquiterpenes from zedoariae rhizoma on d-galactosamine / lipopolysaccharide-induced liver injury
inferredcites →https://doi.org/10.1016/s0968-0896(00)00306-0openalex-snapshot
Hepatoprotective constituents from Zedoariae Rhizoma: absolute stereostructures of three new carabrane-type sesquiterpenes, curcumenolactones A, B, and C
inferredcites →https://doi.org/10.1021/ja01022a027openalex-snapshot
Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds
inferredcites →https://doi.org/10.1021/np000496yopenalex-snapshot
Six New Diarylheptanoids from the Seeds of Alpinia blepharocalyx
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inferredcites →https://doi.org/10.1021/np100392mopenalex-snapshot
Diarylheptanoids from the Rhizomes of Curcuma kwangsiensis
inferredcites →https://doi.org/10.1021/np3002833openalex-snapshot
Alkaloids from the Root of Isatis indigotica
inferredcites →https://doi.org/10.1055/s-2005-871216openalex-snapshot
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inferredcites →https://doi.org/10.1055/s-2006-957473openalex-snapshot
The Griess Assay: Suitable for a Bio-Guided Fractionation of Anti-Inflammatory Plant Extracts?
inferredcites →https://doi.org/10.1080/10286020903042358openalex-snapshot
Guaiane-type sesquiterpenes fromCurcuma wenyujinand their inhibitory effects on nitric oxide production
inferredcites →https://doi.org/10.1093/ecam/nel008openalex-snapshot
Comparison of Anti‐inflammatory Activities of Six Curcuma Rhizomes: A Possible Curcuminoid‐independent Pathway Mediated by Curcuma phaeocaulis Extract
inferredcites →https://doi.org/10.1158/0008-5472.can-06-3066openalex-snapshot
Curcumin, a Dietary Component, Has Anticancer, Chemosensitization, and Radiosensitization Effects by Down-regulating the MDM2 Oncogene through the PI3K/mTOR/ETS2 Pathway
inferredcites →https://doi.org/10.1177/1934578x1200700406openalex-snapshot
Transannular Cyclization of (4 S ,5 S )-Germacrone-4,5-epoxide into Guaiane and Secoguaiane-type Sesquiterpenes
inferredcites →https://doi.org/10.1186/1472-6882-8-55openalex-snapshot
Neuroprotective efficacy and therapeutic window of curcuma oil: in rat embolic stroke model
inferredcites →https://doi.org/10.1246/cl.1980.1625openalex-snapshot
RATES OF DISSOCIATION OF N,N-DIBENZYLANILINIUM IONS IN APROTIC SOLVENTS
inferredcites →https://doi.org/10.1246/cl.1991.1625openalex-snapshot
Structure of Aerugidiol, a New Bridge-head Oxygenated Guaiane Sesquiterpene
inferredcites →https://doi.org/10.1248/cpb.34.434openalex-snapshot
Chemical conversion of (4S,5S)-(+)-germacrone 4,5-epoxide, a plausible biogenetic intermediate found in the essential oil of Zedoariae rhizoma from Yakushima, Japan.
inferredcites →https://doi.org/10.1248/cpb.35.53openalex-snapshot
Structures of sesquiterpenes from Curcuma aromatica Salisb.
inferredcites →https://doi.org/10.1248/cpb.38.55openalex-snapshot
Structures of sesquiterpenes of Curcuma aromatica Salisb. II. Studies on minor sesquiterpenes.
inferredcites →https://doi.org/10.1248/cpb.42.1813openalex-snapshot
Crude Drugs from Aquatic Plants. IV. On the Constituents of Alismatis Rhizoma. (2). Stereostructures of Bioactive Sesquiterpenes, Alismol, Alismoxide, Orientalols A, B, and C, from Chinese Alismatis Rhizoma.
inferredcites →https://doi.org/10.1248/cpb.49.1558openalex-snapshot
Medicinal Foodstuffs. XXVIII. Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol, Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma.
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.2022.113164zenodo-depositor-declared
Guaiane-type sesquiterpenes from Curcuma wenyujin
inferred← citeshttps://doi.org/10.1002/cbdv.201900123openalex-snapshot
Sesquiterpenoid Compounds from Curcuma kwangsiensis
inferred← citeshttps://doi.org/10.1002/cbdv.202400098openalex-snapshot
Curcumae Radix: A Review of Traditional Use, Phytochemistry, Pharmacology, Toxicology and Quality Control
inferred← citeshttps://doi.org/10.1002/ejoc.201402465openalex-snapshot
Eudesmane‐Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Activities on Nitric Oxide Production in RAW 264.7 Cells
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Inducible nitric oxide synthase inhibitors: A comprehensive update
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Iodine and DMSO as Surrogate of Hazardous Metal and Non‐Metal Reagents in Organic Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-031-29006-0_19-1openalex-snapshot
Bioactive Compounds and Biological Activities of Curcuma Species
inferred← citeshttps://doi.org/10.1007/978-3-031-44746-4_19openalex-snapshot
Bioactive Compounds and Biological Activities of Curcuma Species
inferred← citeshttps://doi.org/10.1007/s10600-025-04837-6openalex-snapshot
Three New Sesquiterpenoids from Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1007/s11101-026-10219-9openalex-snapshot
Research progress on chemical constituents from Curcumae Rhizoma, and their pharmacological activity and biosynthesis
inferred← citeshttps://doi.org/10.1016/b978-0-444-63603-4.00004-8openalex-snapshot
Multitargeted Bioactive Materials of Plants in the Curcuma Genus and Related Compounds: Recent Advances
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.01.013openalex-snapshot
Orobanone analogues from acid-promoted aromatization rearrangement of curcumol inhibit hypoxia-inducible factor-1 (HIF-1) in cell-based reporter assays
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103267openalex-snapshot
STAT3-inhibitory activity of sesquiterpenoids and diterpenoids from Curcuma phaeocaulis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103820openalex-snapshot
Seven pairs of new enantiomeric sesquiterpenoids from Curcuma phaeocaulis
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.08.092openalex-snapshot
β-Elemene attenuates atherosclerosis in apolipoprotein E-deficient mice via restoring NO levels and alleviating oxidative stress
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.05.037openalex-snapshot
Two pairs of farnesyl phenolic enantiomers as natural nitric oxide inhibitors from Ganoderma sinense
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104579openalex-snapshot
Terpenoids from the roots of Chloranthus henryi Hemsl. var. hupehensis (Pamp.) K. F. Wu and their chemotaxonomic significance
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Cytotoxic sesquiterpenes and diterpenes from the rhizomes of Curcuma zedoaroides Chaveer. & Tanee
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.03.043openalex-snapshot
Sesquiterpenoids from Curcuma wenyujin dreg and their biological activities
inferred← citeshttps://doi.org/10.1016/j.cjac.2022.100167openalex-snapshot
Rapid identification for the species discrimination of Curcumae Rhizoma using spectrophotometry and flash gas chromatography e-nose combined with chemometrics
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.03.020openalex-snapshot
Cadinane sesquiterpenes from Curcuma phaeocaulis with their inhibitory activities on nitric oxide production in RAW 264.7 cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.03.021openalex-snapshot
Sesquiterpenes from the essential oil of Curcuma wenyujin and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.03.015openalex-snapshot
Caroguaianolide A–E, five new cytotoxic sesquiterpene lactones from Carpesium abrotanoides L.
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112935openalex-snapshot
Anti-inflammatory and antinociceptive effects of Curcuma kwangsiensis and its bioactive terpenoids in vivo and in vitro
inferred← citeshttps://doi.org/10.1016/j.jep.2020.113689openalex-snapshot
Review of the traditional uses, phytochemistry, and pharmacology of Curcuma wenyujin Y. H. Chen et C. Ling
inferred← citeshttps://doi.org/10.1016/j.jep.2026.122246openalex-snapshot
Unlocking the therapeutic potential of Curcuma phaeocaulis Valeton: An integrative review of its ethnopharmacology, processing with vinegar, and pharmacological mechanisms
inferred← citeshttps://doi.org/10.1016/j.jpba.2021.114144openalex-snapshot
High performance liquid chromatography fingerprint and headspace gas chromatography-mass spectrometry combined with chemometrics for the species authentication of Curcumae Rhizoma
inferred← citeshttps://doi.org/10.1016/j.jpba.2021.114145openalex-snapshot
UV spectroscopy and HPLC combined with chemometrics for rapid discrimination and quantification of Curcumae Rhizoma from three botanical origins
inferred← citeshttps://doi.org/10.1016/j.molcatb.2015.01.005openalex-snapshot
Stereo- and regiospecific biotransformation of curcumenol by four fungal strains
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112293openalex-snapshot
Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114592openalex-snapshot
Norsesquiterpenoids from terrestrial and marine organisms: Chemistry, activity and possible biosynthetic pathways (1963–2024)
inferred← citeshttps://doi.org/10.1016/j.phytol.2014.05.009openalex-snapshot
Guaianolides from Curcuma kwangsiensis
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.10.017openalex-snapshot
Four new sesquiterpenoids as natural nitric oxide (NO) inhibitors from the rhizomes of Curcuma phaeocaulis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.079openalex-snapshot
Antimicrobial and anti-inflammatory compounds from a marine fungus Pleosporales sp.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00062openalex-snapshot
Gelstriamine A, a Triamino Monoterpene Indole Alkaloid with a Caged 6/5/7/6/6/5 Scaffold and Analgesic Alkaloids from Gelsemium elegans Stems
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00165openalex-snapshot
Cafestol-Type Diterpenoids from the Twigs of Tricalysia fruticosa with Potential Anti-inflammatory Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00844openalex-snapshot
Chlorinated Guaiane-Type Sesquiterpene Lactones of Natural Origin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01100openalex-snapshot
Sesqui- and Diterpenoids from the Radix of Curcuma aromatica
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00690openalex-snapshot
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated fromPogostemon cablin
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01907openalex-snapshot
Collective Syntheses of Guaiane Sesquiterpenes: Stereoselective Syntheses of (+)-Dysodensiol F, (+)-10β,14-Dihydroxy-allo-aromadendrane, and (−)-Dendroside C Aglycon
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03971openalex-snapshot
Four-Step Synthesis of (±)-Nanolobatolide via Site-Selective Functionalization
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Stereoselective Synthesis of 1,4,5-Tri-cis-guaiane Sesquiterpene: First Total Synthesis of (−)-Dendroside C Aglycon
inferred← citeshttps://doi.org/10.1021/acscatal.3c00132openalex-snapshot
Fully Biocatalytic Rearrangement of Furans to Spirolactones
inferred← citeshttps://doi.org/10.1021/jacs.2c02188openalex-snapshot
Asymmetric Total Synthesis of (−)-Phaeocaulisin A
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inferred← citeshttps://doi.org/10.1021/jacs.4c12121openalex-snapshot
Ten-Step Total Synthesis of (±)-Phaeocaulisin A Enabled by Cyclopropanol Ring-Opening Carbonylation
inferred← citeshttps://doi.org/10.1021/np400873vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np400984copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np500845zopenalex-snapshot
Biotransformation of Curcumenol by Mucor polymorphosporus
inferred← citeshttps://doi.org/10.1021/np500951sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-017-18841-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/srep43576openalex-snapshot
(+)/(−)-Phaeocaulin A-D, four pairs of new enantiomeric germacrane-type sesquiterpenes from Curcuma phaeocaulis as natural nitric oxide inhibitors
inferred← citeshttps://doi.org/10.1039/c4cc02641aopenalex-snapshot
Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls
inferred← citeshttps://doi.org/10.1039/c4ra13136copenalex-snapshot
Sesquiterpenoids isolated from an endophyte fungus Diaporthe sp.
inferred← citeshttps://doi.org/10.1039/c5ob00964bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c7np00043jopenalex-snapshot
Recent progress in the isolation, bioactivity, biosynthesis, and total synthesis of natural spiroketals
inferred← citeshttps://doi.org/10.1039/c8fo02549eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8nj02027bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9cc09159aopenalex-snapshot
Pseudoguaianelactones A–C: three unusual sesquiterpenoids from Lindera glauca with anti-inflammatory activities by inhibiting the LPS-induced expression of iNOS and COX-2
inferred← citeshttps://doi.org/10.1039/d1ra08631fopenalex-snapshot
Guaiane sesquiterpenes from the gorgonian Echinogorgia flora collected in the South China Sea
inferred← citeshttps://doi.org/10.1039/d2nj06011fopenalex-snapshot
Sesquiterpenoids isolated from the rhizome of Curcuma phaeocaulis Valeton: antitumor activity, in silico molecular docking and molecular dynamics study
inferred← citeshttps://doi.org/10.1039/d2qo01261hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3ra08686kopenalex-snapshot
Sesquiterpenoids and hexanorcucurbitacin from Aquilaria malaccensis agarwood with anti-inflammatory effects by inhibiting the STAT1/AKT/MAPK/NLRP3 pathway
inferred← citeshttps://doi.org/10.1055/a-0668-0962openalex-snapshot
Diarylheptanoids from Curcuma phaeocaulis Suppress IL-6-Induced STAT3 Activation
inferred← citeshttps://doi.org/10.1055/a-1326-9148openalex-snapshot
Total Synthesis of (±)-Phaeocaulisin D
inferred← citeshttps://doi.org/10.1055/a-2706-0821openalex-snapshot
Total Synthesis of (±)-Phaeocaulisin A Enabled Chemistry Innovation and Biological Discovery
inferred← citeshttps://doi.org/10.1080/10286020.2015.1046449openalex-snapshot
Four new sesquiterpenes from the rhizomes ofCurcuma phaeocaulisand their iNOS inhibitory activities
inferred← citeshttps://doi.org/10.1080/10286020.2023.2249833openalex-snapshot
Two new guaiane-type sesquiterpenes from Curcuma wenyujin
inferred← citeshttps://doi.org/10.1080/10408398.2016.1176554openalex-snapshot
Chemical constituents and biological research on plants in the genus Curcuma
inferred← citeshttps://doi.org/10.1080/10942912.2017.1387556openalex-snapshot
Nutritional value, phytochemical composition, and biological activities of edible Curcuma species: A review
inferred← citeshttps://doi.org/10.1080/14786419.2016.1205053openalex-snapshot
Sesquiterpenes from Curcuma wenyujin with their inhibitory activities on nitric oxide production in RAW 264.7 cells
inferred← citeshttps://doi.org/10.1080/14786419.2020.1806273openalex-snapshot
New phenylpropanoids from the fruits of Xanthium sibiricum and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1139/cjc-2019-0456openalex-snapshot
Metal-free oxidative C(sp3)–H functionalization: a facile route to quinoline formaldehydes from methyl-azaheteroarenes
inferred← citeshttps://doi.org/10.1155/2016/4973128openalex-snapshot
Two Traditional Chinese Medicines Curcumae Radix and Curcumae Rhizoma: An Ethnopharmacology, Phytochemistry, and Pharmacology Review
inferred← citeshttps://doi.org/10.1177/17448069221121562openalex-snapshot
The analgesic effects of β-elemene in rats with neuropathic pain by inhibition of spinal astrocytic ERK activation
inferred← citeshttps://doi.org/10.1177/1934578x1801300105openalex-snapshot
A New Guaiane-type Sesquiterpenoid from a Bornean Soft Coral, Xenia stellifera
inferred← citeshttps://doi.org/10.1177/1934578x241301999openalex-snapshot
Molecular Mechanism of Sangmei Zhike Granules in Treating Allergic Asthma: Insights from UPLC-MS/MS and Network Pharmacology
inferred← citeshttps://doi.org/10.1248/cpb.c16-00086openalex-snapshot
Sesquiterpenoids from the Rhizomes of Curcuma phaeocaulis and Their Inhibitory Effects on LPS-Induced TLR4 Activation
inferred← citeshttps://doi.org/10.3390/biom14040387openalex-snapshot
Research Progress on Sesquiterpenoids of Curcumae Rhizoma and Their Pharmacological Effects
inferred← citeshttps://doi.org/10.3390/molecules22071206openalex-snapshot
Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl
inferred← citeshttps://doi.org/10.3390/plants10010063openalex-snapshot
The Genus Curcuma and Inflammation: Overview of the Pharmacological Perspectives
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