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iNOS Inhibitory Activity of Sesquiterpenoids and a Monoterpenoid from the Rhizomes of Curcuma wenyujin

https://doi.org/10.1021/np400984c
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Electronic CD Exciton Chirality Method: Principles and Applications
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Four New Sesquiterpenes from Curcuma wenyujin and Their Inhibitory Effects on Nitric‐Oxide Production
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Structures of antifungal diarylheptenones, gingerenones A, B, C and isogingerenone B, isolated from the rhizomes of Zingiber officinale
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Guaiane sesquiterpene lactones from Curcuma aeruginosa
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Pentacyclic hemiacetal sterol with antifouling and cytotoxic activities from the soft coral Nephthea sp.
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Cytotoxic diterpenes from the radix of Curcuma wenyujin
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Zedoarol, 13-hydroxygermacrone and curzeone, three sesquiterpenoids from Curcuma zedoaria
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Circulardichroismus—VIII
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[Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols
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Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds
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Discovery of Natural Products from Curcuma longa that Protect Cells from Beta-Amyloid Insult: A Drug Discovery Effort against Alzheimer's Disease
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Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production
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Cytotoxicity of Curcuminoids and Some Novel Compounds from Curcuma zedoaria
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Guaiane-type sesquiterpenes fromCurcuma wenyujinand their inhibitory effects on nitric oxide production
inferredcites →https://doi.org/10.1093/chromsci/bmt149openalex-snapshot
Quantitative Analysis and Discrimination of Steamed and Non-Steamed Rhizomes of Curcuma wenyujin by GC–MS and HPLC
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
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A reinvestigation of the structure of zederone, a furanogermacrane-type sesquiterpene from zedoary.
inferredcites →https://doi.org/10.1248/cpb.38.55openalex-snapshot
Structures of sesquiterpenes of Curcuma aromatica Salisb. II. Studies on minor sesquiterpenes.
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Inhibitors of Nitric Oxide Production and New Sesquiterpenes, 4-epi-Curcumenol, Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B from Zedoariae Rhizoma
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Biologically Active Secondary Metabolites from the Ascomycete A111-95 2. Structure Elucidation.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Polyprenylated acylphloroglucinols from Hypericum monogynum and their reversal of multidrug resistance in MCF-7/ADR cells
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Sesquiterpenes from Curcuma zedoaria rhizomes and their cytotoxicity against human gastric cancer AGS cells
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Guaiane-type sesquiterpenoids with various ring skeletons from Daphne bholua uncovered by molecular networking and structural revisions of previously reported analogues
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Terpenoids from Curcuma wenyujin increased glucose consumption on HepG2 cells
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Curcuma wenyujin rhizomes extract ameliorates lipid accumulation
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112935openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jep.2020.113689openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phymed.2024.156098openalex-snapshot
The processing mechanism of vinegar-processed Curcumae Rhizome enhances anti hepatic fibrotic effects through regulation of PI3K/Akt/mTOR signaling pathway
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114353openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytol.2018.07.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytol.2022.11.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytol.2025.104068openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152448openalex-snapshot
Wenyujindiol A, a new sesquiterpene from the rhizomes of Curcuma wenyujin
inferred← citeshttps://doi.org/10.1021/acs.jafc.5b01584openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00185openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01100openalex-snapshot
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Minimalist Relativistic Force Field: Prediction of Proton–Proton Coupling Constants in 1H NMR Spectra Is Perfected with NBO Hybridization Parameters
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Organophotocatalytic Radical Chloro-fluorosulfonylation of Alkynyl Cyclohexadienones
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Catalytic Enantioselective Intermolecular [5 + 2] Dipolar Cycloadditions of a 3-Hydroxy-4-pyrone-Derived Oxidopyrylium Ylide
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Asymmetric Total Synthesis of (−)-Phaeocaulisin A
inferred← citeshttps://doi.org/10.1021/jacs.4c12121openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c5ob00964bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/a-2706-0821openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10286020.2015.1046449openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10408398.2016.1176554openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biom14040387openalex-snapshot
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Nitric Oxide Synthase Inhibitors
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