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Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line

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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/chir.1067openalex-snapshot
Chiroptical properties of 2,3‐dihydrobenzo[b]furan and chromane chromophores in naturally occurring O‐heterocycles
inferredcites →https://doi.org/10.1002/chir.22571openalex-snapshot
Enantiomeric Neolignans and a Sesquiterpene from Solanum erianthum and Their Absolute Configuration Assignment
inferredcites →https://doi.org/10.1002/hlca.201000116openalex-snapshot
Neolignans and Caffeoyl Derivatives from Selaginella moellendorffii
inferredcites →https://doi.org/10.1002/hlca.201500002openalex-snapshot
Three New Lignan Derivatives from Lindera glauca ( Siebold et Zucc .) Blume
inferredcites →https://doi.org/10.1002/jlac.198319831218openalex-snapshot
Circulardichroismus, LXXXI. Synthese und Circulardichroismus von Steroiden mit Isochromanon‐Chromophor
inferredcites →https://doi.org/10.1002/jlac.1991199101115openalex-snapshot
Synthesis and circular dichroism of steroids with a 1,4‐benzodioxane chromophore: On the absolute configuration of (−)‐silandrin
inferredcites →https://doi.org/10.1002/poc.3335openalex-snapshot
Visible light‐induced diastereoselectiveE/Z‐photoisomerization equilibrium of the C=C benzofuran‐3‐one‐hydantoin dyad
inferredcites →https://doi.org/10.1002/poc.3534openalex-snapshot
Chemistry and photochemistry of natural plant pigments: the anthocyanins
inferredcites →https://doi.org/10.1007/s10086-007-0892-xopenalex-snapshot
Biosynthesis of lignans and norlignans
inferredcites →https://doi.org/10.1007/s13659-016-0095-5openalex-snapshot
Neolignans from Selaginella moellendorffii
inferredcites →https://doi.org/10.1016/1010-6030(90)87014-3openalex-snapshot
Preparation of two novel spermine alkaloids by E/Z isomerisation of the cinnamoyl chromophore
inferredcites →https://doi.org/10.1016/j.bmcl.2013.08.045openalex-snapshot
The cytotoxicity of 8-O-4′ neolignans from the seeds of Crataegus pinnatifida
inferredcites →https://doi.org/10.1016/j.bmcl.2015.03.015openalex-snapshot
(+)- and (−)-liriodenol, a pair of novel enantiomeric lignans from Liriodendron hybrid
inferredcites →https://doi.org/10.1016/j.chroma.2011.07.093openalex-snapshot
Enantiomeric resolution of (±)-licarin A by high-performance liquid-chromatography using a chiral stationary phase
inferredcites →https://doi.org/10.1016/j.copbio.2005.06.010openalex-snapshot
Dirigent phenoxy radical coupling: advances and challenges
inferredcites →https://doi.org/10.1016/j.fitote.2012.12.028openalex-snapshot
Neolignans from leaves of Miliusa mollis
inferredcites →https://doi.org/10.1016/j.fitote.2013.09.011openalex-snapshot
Cytotoxic and antioxidant dihydrobenzofuran neolignans from the seeds of Crataegus pinnatifida
inferredcites →https://doi.org/10.1016/j.fitote.2016.03.012openalex-snapshot
Rational quality assessment procedure for less-investigated herbal medicines: Case of a Congolese antimalarial drug with an analytical report
inferredcites →https://doi.org/10.1016/j.jep.2005.02.020openalex-snapshot
Ethnobotanical study of some Ghanaian anti-malarial plants
inferredcites →https://doi.org/10.1016/j.phytol.2013.03.009openalex-snapshot
Two new dihydrobenzofuran-type neolignans from Breynia fruticosa
inferredcites →https://doi.org/10.1016/j.tet.2006.10.018openalex-snapshot
Synthesis of dihydrodehydrodiconiferyl alcohol and derivatives through intramolecular C–H insertion
inferredcites →https://doi.org/10.1016/j.tet.2013.04.086openalex-snapshot
Rh(II)-catalyzed enantioselective synthesis of acuminatin through a C–H insertion reaction of a non-stabilized carbenoid
inferredcites →https://doi.org/10.1016/s0031-9422(02)00573-3openalex-snapshot
Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde capillary zone electrophoresis study of pH effect
inferredcites →https://doi.org/10.1016/s0040-4020(00)00873-5openalex-snapshot
Stereoselective Synthesis of 8,9-Licarinediols
inferredcites →https://doi.org/10.1016/s0040-4020(01)97775-0openalex-snapshot
Circular dichroism—XLVI
inferredcites →https://doi.org/10.1016/s0040-4020(98)00725-xopenalex-snapshot
On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton
inferredcites →https://doi.org/10.1016/s0040-4039(02)01319-9openalex-snapshot
Prevention of UV-light induced E,Z-isomerization of caffeoyl residues in the diacylated anthocyanin, gentiodelphin, by intramolecular stacking
inferredcites →https://doi.org/10.1016/s1369-703x(02)00217-6openalex-snapshot
Influence of E,Z-isomerization and stability of acylated anthocyanins under the UV irradiation
inferredcites →https://doi.org/10.1021/ac990001dopenalex-snapshot
HPLC−CD On-Line Coupling in Combination with HPLC−NMR and HPLC−MS/MS for the Determination of the Full Absolute Stereostructure of New Metabolites in Plant Extracts
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00220openalex-snapshot
Neolignans from Aristolochia fordiana Prevent Oxidative Stress-Induced Neuronal Death through Maintaining the Nrf2/HO-1 Pathway in HT22 Cells
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00328openalex-snapshot
(±)-Acortatarinowins A–F, Norlignan, Neolignan, and Lignan Enantiomers from Acorus tatarinowii
inferredcites →https://doi.org/10.1021/ed039p333openalex-snapshot
The Beer-Lambert Law
inferredcites →https://doi.org/10.1021/jf1041933openalex-snapshot
Isolation and Identification of Compounds Responsible for Antioxidant Capacity of Euryale ferox Seeds
inferredcites →https://doi.org/10.1021/jo900502dopenalex-snapshot
Asymmetric Synthesis of Neolignans (−)-epi-Conocarpan and (+)-Conocarpan via Rh(II)-Catalyzed C−H Insertion Process and Revision of the Absolute Configuration of (−)-epi-Conocarpan
inferredcites →https://doi.org/10.1021/np100891yopenalex-snapshot
Spirocyclic Lignans from Guaiacum (Zygophyllaceae) Induce Apoptosis in Human Breast Cancer Cell Lines
inferredcites →https://doi.org/10.1021/np200117yopenalex-snapshot
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations
inferredcites →https://doi.org/10.1021/np400070xopenalex-snapshot
Bioactive Dibenzocyclooctadiene Lignans from the Stems of Schisandra neglecta
inferredcites →https://doi.org/10.1021/np500528uopenalex-snapshot
(±)-Torreyunlignans A–D, Rare 8–9′ Linked Neolignan Enantiomers as Phosphodiesterase-9A Inhibitors from Torreya yunnanensis
inferredcites →https://doi.org/10.1021/np5008153openalex-snapshot
Neolignans and Other Metabolites from Ocotea cymosa from the Madagascar Rain Forest and Their Biological Activities
inferredcites →https://doi.org/10.1021/np500951sopenalex-snapshot
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum
inferredcites →https://doi.org/10.1021/np5010533openalex-snapshot
Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium
inferredcites →https://doi.org/10.1021/np50119a024openalex-snapshot
Isolation and Structure Elucidation of Xylobuxin, a New Neolignan from Xylopia buxifolia
inferredcites →https://doi.org/10.1021/np800488popenalex-snapshot
Antioxidant Lignans from the Fruits of Broussonetia papyrifera
inferredcites →https://doi.org/10.1021/ol502649aopenalex-snapshot
Chiral Resolution and Absolute Configuration of a Pair of Rare Racemic Spirodienone Sesquineolignans from Xanthium sibiricum
inferredcites →https://doi.org/10.1023/b:phyt.0000045497.90158.d2openalex-snapshot
Lignans and neolignans as lead compounds
inferredcites →https://doi.org/10.1038/nrd915openalex-snapshot
Putting chirality to work: the strategy of chiral switches
inferredcites →https://doi.org/10.1038/srep22909openalex-snapshot
Antioxidant Lignans and Neolignans from Acorus tatarinowii
inferredcites →https://doi.org/10.1038/srep24809openalex-snapshot
Enantiomeric Lignans and Neolignans from Phyllanthus glaucus: Enantioseparation and Their Absolute Configurations
inferredcites →https://doi.org/10.1039/b302632aopenalex-snapshot
Synthesis and chiral HPLC analysis of the dibenzyltetrahydrofuran lignans, larreatricins, 8′-epi-larreatricins, 3,3′-didemethoxyverrucosins and meso-3,3′-didemethoxynectandrin B in the creosote bush (Larrea tridentata): evidence for regiospecific control of coupling
inferredcites →https://doi.org/10.1039/b413742fopenalex-snapshot
Polyamine alkaloids
inferredcites →https://doi.org/10.1039/b514045popenalex-snapshot
An update on bioactive plant lignans
inferredcites →https://doi.org/10.1039/b910940dopenalex-snapshot
An update on lignans: natural products and synthesis
inferredcites →https://doi.org/10.1039/c1np00044fopenalex-snapshot
Flavonoids and their glycosides, including anthocyanins
inferredcites →https://doi.org/10.1039/c6np00021eopenalex-snapshot
Recent advances in research on lignans and neolignans
inferredcites →https://doi.org/10.1055/s-2003-39316openalex-snapshot
An Efficient Synthesis of OpticallyActivetrans-2-Aryl-2,3-dihydrobenzofuran-3-carboxylicAcid Esters via C-H Insertion Reaction
inferredcites →https://doi.org/10.1055/s-2007-969270openalex-snapshot
A New Neo-Lignan, A Prostaglandin I2Inducer from the Leaves ofZizyphus jujuba
inferredcites →https://doi.org/10.1111/bcpt.12639openalex-snapshot
In Vitro Effects of the Neolignan 2,3‐Dihydrobenzofuran Against Leishmania Amazonensis
inferredcites →https://doi.org/10.1248/cpb.40.2099openalex-snapshot
Chemical and Chemotaxonomical Studies of Ferns. LXXXI. Characteristic Lignans of Blechnaceous Ferns.
inferredcites →https://doi.org/10.1248/cpb.53.641openalex-snapshot
Aromatic Constituents from the Heartwood of Santalum album L.
inferredcites →https://doi.org/10.1248/cpb.58.587openalex-snapshot
Lignans from Santalum album and Their Cytotoxic Activities
inferredcites →https://doi.org/10.1248/cpb.c13-00668openalex-snapshot
Three New Lignan Glycosides with IL-6 Inhibitory Activity from Akebia quinata
inferredcites →https://doi.org/10.3762/bjoc.10.313openalex-snapshot
Trogopterins A–C: Three new neolignans from feces of Trogopterus xanthipes
inferredcites →https://doi.org/10.3923/rjpharm.2010.45.50openalex-snapshot
Anti-Plasmodial and Larvicidal Effects of Surface Exudates ofGardenia ternifolia Aerial Parts
inferredcites →https://doi.org/10.5194/bg-11-1435-2014openalex-snapshot
Laboratory and field measurements of enantiomeric monoterpene emissions as a function of chemotype, light and temperature
inferredcites →https://doi.org/10.7314/apjcp.2016.17.4.1655openalex-snapshot
Celecoxib, a COX-2 Selective Inhibitor, Induces Cell Cycle Arrest at the G2/M Phase in HeLa Cervical Cancer Cells

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/chir.23360openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.03.043openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chroma.2018.07.039openalex-snapshot
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Phenylpropanoids from the fruit of Crataegus pinnatifida exhibit cytotoxicity on hepatic carcinoma cells through apoptosis induction
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105228openalex-snapshot
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Aromatic glycosides and lignans glycosides with their acetylcholinesterase inhibitory activities from the leaves of Picrasma quassioides
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112417openalex-snapshot
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Neurotrophic phenolic glycosides from the roots of Armoracia rusticana
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Bioactive metabolites from marine-derived Streptomyces sp. A68 and its Rifampicin resistant mutant strain R-M1
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Thunbergiside A: An unprecedented neolignan isolated from Gardenia thunbergia L. f. and the antifungal activity of selected phytochemicals
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