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Minor Nortriterpenoids from the Twigs and Leaves of Rhododendron latoucheae

https://doi.org/10.1021/acs.jnatprod.7b01074
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What this work says

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

inferredcites →https://doi.org/10.1002/rcm.3069openalex-snapshot
Rapid structural determination of new trace cassaine‐type diterpenoid amides in fractions from Erythrophleum fordii by liquid chromatography‐diode‐array detection/electrospray ionization tandem mass spectrometry and liquid chromatography/nuclear magnetic resonance
inferredcites →https://doi.org/10.1016/j.bmc.2005.10.063openalex-snapshot
Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2
inferredcites →https://doi.org/10.1016/j.fitote.2011.09.012openalex-snapshot
Sesquiterpenoids and norterpenoids from Vitex negundo
inferredcites →https://doi.org/10.1016/j.pbb.2013.07.020openalex-snapshot
Ursolic acid from Agastache mexicana aerial parts produces antinociceptive activity involving TRPV1 receptors, cGMP and a serotonergic synergism
inferredcites →https://doi.org/10.1016/j.phytochem.2005.11.026openalex-snapshot
Beccaridiol, an unusual 28-nortriterpenoid from the leaves of Diplectria beccariana
inferredcites →https://doi.org/10.1016/s0031-9422(99)00316-7openalex-snapshot
Triterpene phytoalexins from nectarine fruits
inferredcites →https://doi.org/10.1016/s0040-4020(01)96931-5openalex-snapshot
Optical activity of non-planar conjugated dienes—II
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00603openalex-snapshot
Magnetic Ligand Fishing as a Targeting Tool for HPLC-HRMS-SPE-NMR: α-Glucosidase Inhibitory Ligands and Alkylresorcinol Glycosides from Eugenia catharinae
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Antiviral Spirotriscoumarins A and B: Two Pairs of Oligomeric Coumarin Enantiomers with a Spirodienone–Sesquiterpene Skeleton from Toddalia asiatica
inferredcites →https://doi.org/10.1021/bk-2006-0936.ch005openalex-snapshot
Powerful Analytical Tools for Citrus Characterization: LC/MS and LC/NMR Characterization of Polymethoxylated Flavones
inferredcites →https://doi.org/10.1021/ja00729a024openalex-snapshot
.pi.-.pi.* Region Cotton effects of cyclic conjugated dienes and enones. Interpretation in terms of allylic axial chirality contributions
inferredcites →https://doi.org/10.1021/jf101847eopenalex-snapshot
Separation and Identification of Phenolic Compounds of Extra Virgin Olive Oil from Olea europaea L. by HPLC-DAD-SPE-NMR/MS. Identification of a New Diastereoisomer of the Aldehydic Form of Oleuropein Aglycone
inferredcites →https://doi.org/10.1021/jf204406uopenalex-snapshot
Identification of Three Novel Polyphenolic Compounds, Origanine A–C, with Unique Skeleton from Origanum vulgare L. Using the Hyphenated LC-DAD-SPE-NMR/MS Methods
inferredcites →https://doi.org/10.1021/jf402949yopenalex-snapshot
High-Resolution Screening Combined with HPLC-HRMS-SPE-NMR for Identification of Potential Health-Promoting Constituents in Sea Aster and Searocket—New Nordic Food Ingredients
inferredcites →https://doi.org/10.1021/jf501605zopenalex-snapshot
High-Resolution Screening Combined with HPLC-HRMS-SPE-NMR for Identification of Fungal Plasma Membrane H+-ATPase Inhibitors from Plants
inferredcites →https://doi.org/10.1021/jm5014067openalex-snapshot
Discovery of Pentacyclic Triterpenoids as Potential Entry Inhibitors of Influenza Viruses
inferredcites →https://doi.org/10.1021/np060454vopenalex-snapshot
Isolation and Structure Elucidation by LC-MS-SPE/NMR: PR Toxin- and Cuspidatol-Related Eremophilane Sesquiterpenes from Penicillium roqueforti
inferredcites →https://doi.org/10.1021/np070125iopenalex-snapshot
Minor Sesquiterpene Lactones from Centaurea pullata and Their Antimicrobial Activity
inferredcites →https://doi.org/10.1021/np1007922openalex-snapshot
Anti-inflammatory Triterpenes from the Leaves of Rosa laevigata
inferredcites →https://doi.org/10.1021/np5009416openalex-snapshot
Dual High-Resolution α-Glucosidase and Radical Scavenging Profiling Combined with HPLC-HRMS-SPE-NMR for Identification of Minor and Major Constituents Directly from the Crude Extract of Pueraria lobata
inferredcites →https://doi.org/10.1021/np800010ropenalex-snapshot
Combining HPLC-PDA-MS-SPE-NMR with Circular Dichroism for Complete Natural Product Characterization in Crude Extracts: Levorotatory Gossypol inThespesia danis
inferredcites →https://doi.org/10.1021/np800562mopenalex-snapshot
FTICR-MS and LC-UV/MS-SPE-NMR Applications for the Rapid Dereplication of a Crude Extract from the Sponge Ianthella flabelliformis
inferredcites →https://doi.org/10.1021/np900237aopenalex-snapshot
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
inferredcites →https://doi.org/10.1021/np9005025openalex-snapshot
LC-MS-SPE-NMR for the Isolation and Characterization of neo-Clerodane Diterpenoids from Teucrium luteum subsp. flavovirens
inferredcites →https://doi.org/10.1021/np970416zopenalex-snapshot
Combination of LC−MS and LC−NMR as a Tool for the Structure Determination of Natural Products
inferredcites →https://doi.org/10.1021/ol302660topenalex-snapshot
Enantiomers of an Indole Alkaloid Containing Unusual Dihydrothiopyran and 1,2,4-Thiadiazole Rings from the Root of Isatis indigotica
inferredcites →https://doi.org/10.1021/ol501760hopenalex-snapshot
A Minor Diterpenoid with a New 6/5/7/3 Fused-Ring Skeleton from Euphorbia micractina
inferredcites →https://doi.org/10.1038/s41598-017-06320-xopenalex-snapshot
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR
inferredcites →https://doi.org/10.1038/sj.jim.7000057openalex-snapshot
LC-NMR: a new tool to expedite the dereplication and identification of natural products
inferredcites →https://doi.org/10.1039/c1ay05287jopenalex-snapshot
Separation and structural characterization of a synthetic cannabinoid found in a herbal product using off-line LC-DAD-NMR
inferredcites →https://doi.org/10.1080/14786419.2014.980249openalex-snapshot
A new triterpenoid from the fruits of Gardenia jasminoides var. radicans Makino
inferredcites →https://doi.org/10.1080/14786419.2015.1007456openalex-snapshot
Inhibitory effects of lupene-derived pentacyclic triterpenoids fromBursera simarubaon HSV-1 and HSV-2in vitroreplication
inferredcites →https://doi.org/10.1248/cpb.57.532openalex-snapshot
Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki
inferredcites →https://doi.org/10.5107/sccj.35.4_298openalex-snapshot
Development of Semimicro LC/NMR and Its Applications in Cosmetic Ingredients Analysis.

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.2021.113083zenodo-depositor-declared
Terpenoids with α-glucosidase inhibitory activity from Rhododendron minutiflorum Hu
inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00013-9openalex-snapshot
Triterpenoids and saponins in drug discovery
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.104955openalex-snapshot
Chemical constituents and hepatoprotective properties of Rhododendron simsii Planch extract in Con A-induced autoimmune hepatitis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104866openalex-snapshot
Oxygenated pentacyclic triterpenoids from the stems and branches of Enkianthus chinensis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106375openalex-snapshot
Ganoapplins A and B with an unprecedented 6/6/6/5/6-fused pentacyclic skeleton from Ganoderma inhibit Tau pathology through activating autophagy
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145760openalex-snapshot
Discovery of diverse skeletons triterpenoid and sesquiterpenoid with anti-inflammatory and PTP1B inhibitory activities from the fruits of Rosa roxburghii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113899openalex-snapshot
An updated review of the genus Rhododendron since 2010: Traditional uses, phytochemistry, and pharmacology
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114200openalex-snapshot
Chromene meroterpenoids from Rhododendron dauricum L. and their anti-inflammatory effects
inferred← citeshttps://doi.org/10.1016/j.tet.2018.11.059openalex-snapshot
Triterpenoids from the twigs and leaves of Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00372openalex-snapshot
Aquilariperoxide A, a Sesquiterpene Dimer from Agarwood of Aquilaria sinensis with Dual Antitumor and Antimalarial Effects
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00295openalex-snapshot
Organocatalytic Enantioselective γ-Elimination: Applications in the Preparation of Chiral Peroxides and Epoxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01891openalex-snapshot
Bioinspired Gram-Scale Synthesis of Alstoscholarinoid B
inferred← citeshttps://doi.org/10.1021/acscatal.0c03231openalex-snapshot
An Unexpected Oxidosqualene Cyclase Active Site Architecture in the Iris tectorum Multifunctional α-Amyrin Synthase
inferred← citeshttps://doi.org/10.1039/d0qo01541eopenalex-snapshot
Xanthanoltrimer A–C: three xanthanolide sesquiterpene trimers from the fruits of Xanthium italicum Moretti isolated by HPLC-MS-SPE-NMR
inferred← citeshttps://doi.org/10.1080/10286020.2019.1585823openalex-snapshot
New glycosides from the twigs and leaves of Rhododendron latoucheae
inferred← citeshttps://doi.org/10.1080/10286020.2021.2007089openalex-snapshot
Two new diterpenoids from the stems of Rhododendron dauricum as GABAA receptor agonists
inferred← citeshttps://doi.org/10.1080/10286020.2024.2313542openalex-snapshot
Triterpenoids from the hook-bearing stems of Uncaria rhynchophylla
inferred← citeshttps://doi.org/10.3389/fphar.2021.599778openalex-snapshot
Multiple Biological Activities of Rhododendron przewalskii Maxim. Extracts and UPLC-ESI-Q-TOF/MS Characterization of Their Phytochemical Composition
inferred← citeshttps://doi.org/10.3389/fphar.2024.1490335openalex-snapshot
Identification of antibacterial constituents from Rhododendron simsii Planch with an activity-guided method
inferred← citeshttps://doi.org/10.3390/molecules28237718openalex-snapshot
Selected Plant Triterpenoids and Their Derivatives as Antiviral Agents
inferred← citeshttps://doi.org/10.3390/plants12162897openalex-snapshot
Insight into the Molecular Mechanism of Flower Color Regulation in Rhododendron latoucheae Franch: A Multi-Omics Approach
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