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Jatrophane Diterpenes as Inhibitors of Chikungunya Virus Replication: Structure–Activity Relationship and Discovery of a Potent Lead

https://doi.org/10.1021/np500271u
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ejoc.201200733openalex-snapshot
Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery
inferredcites →https://doi.org/10.1007/s00280-002-0541-4openalex-snapshot
Biological properties of jatrophane polyesters, new microtubule-interacting agents
inferredcites →https://doi.org/10.1007/s11101-009-9126-8openalex-snapshot
Jatrophane diterpenes from Euphorbia spp. as modulators of multidrug resistance in cancer therapy
inferredcites →https://doi.org/10.1016/0166-0934(88)90134-6openalex-snapshot
Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
inferredcites →https://doi.org/10.1016/j.antiviral.2013.06.009openalex-snapshot
Chikungunya fever: Epidemiology, clinical syndrome, pathogenesis and therapy
inferredcites →https://doi.org/10.1016/j.bcp.2007.12.004openalex-snapshot
Differential effects of phorbol-13-monoesters on human immunodeficiency virus reactivation
inferredcites →https://doi.org/10.1016/j.bcp.2008.11.025openalex-snapshot
SJ23B, a jatrophane diterpene activates classical PKCs and displays strong activity against HIV in vitro
inferredcites →https://doi.org/10.1016/j.drudis.2013.05.002openalex-snapshot
Chikungunya virus: an update on antiviral development and challenges
inferredcites →https://doi.org/10.1016/j.phytochem.2009.10.005openalex-snapshot
Effects of diterpenes from latex of Euphorbia lactea and Euphorbia laurifolia on human immunodeficiency virus type 1 reactivation
inferredcites →https://doi.org/10.1016/j.phytochem.2012.07.023openalex-snapshot
Antiviral chlorinated daphnane diterpenoid orthoesters from the bark and wood of Trigonostemon cherrieri
inferredcites →https://doi.org/10.1016/j.tet.2005.02.031openalex-snapshot
Amygdaloidins A–L, twelve new 13 α-OH jatrophane diterpenes from Euphorbia amygdaloides L.
inferredcites →https://doi.org/10.1016/j.ympev.2011.06.011openalex-snapshot
Giants and dwarfs: Molecular phylogenies reveal multiple origins of annual spurges within Euphorbia subg. Esula
inferredcites →https://doi.org/10.1016/s0024-3205(96)00567-xopenalex-snapshot
Euphorbium: Modern research on its active principle, resiniferatoxin, revives an ancient medicine
inferredcites →https://doi.org/10.1016/s0166-3542(03)00034-2openalex-snapshot
Activation of latent HIV-1 expression by the potent anti-tumor promoter 12-deoxyphorbol 13-phenylacetate
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferredcites →https://doi.org/10.1021/jm00089a006openalex-snapshot
A nonpromoting phorbol from the Samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1
inferredcites →https://doi.org/10.1021/jm400460dopenalex-snapshot
Chikungunya Virus: Emerging Targets and New Opportunities for Medicinal Chemistry
inferredcites →https://doi.org/10.1021/np300637topenalex-snapshot
Prostratin and 12-O-Tetradecanoylphorbol 13-Acetate Are Potent and Selective Inhibitors of Chikungunya Virus Replication
inferredcites →https://doi.org/10.1021/np970507wopenalex-snapshot
Macrocyclic Diterpenoids from Euphorbia semiperfoliata
inferredcites →https://doi.org/10.1021/ol2030907openalex-snapshot
Trigocherrin A, the First Natural Chlorinated Daphnane Diterpene Orthoester from Trigonostemon cherrieri
inferredcites →https://doi.org/10.1080/10915810701464641openalex-snapshot
Phorbol Esters: Structure, Biological Activity, and Toxicity in Animals
inferredcites →https://doi.org/10.1107/s0108767304098800openalex-snapshot
Precise absolute-structure determination in light-atom crystals
inferredcites →https://doi.org/10.1128/jvi.68.3.1962-1969.1994openalex-snapshot
The phorbol ester phorbol myristate acetate inhibits human immunodeficiency virus type 1 envelope-mediated fusion by modulating an accessory component(s) in CD4-expressing cells
inferredcites →https://doi.org/10.1371/journal.pone.0026677openalex-snapshot
Picomolar Dichotomous Activity of Gnidimacrin Against HIV-1
inferredcites →https://doi.org/10.2307/2399909openalex-snapshot
Synopsis of the Genera and Suprageneric Taxa of Euphorbiaceae
inferredcites →https://doi.org/10.3390/molecules19033617openalex-snapshot
Trigocherrierin A, a Potent Inhibitor of Chikungunya Virus Replication
inferredcites →https://doi.org/10.3390/toxins2010174openalex-snapshot
The Protein Kinase C Agonist PEP005 (Ingenol 3-Angelate) in the Treatment of Human Cancer: A Balance between Efficacy and Toxicity
inferredcites →https://doi.org/10.5897/jmpr.9001294openalex-snapshot
Why do Euphorbiaceae tick as medicinal plants? A review of Euphorbiaceae family and its medicinal features

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.2021.112775zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/cbdv.202200918openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ptr.5749openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-58975-2_17openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-83350-3_10-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-12199-9_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-20397-3_3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-10-3421-3_19openalex-snapshot
Antiviral Agents Towards Chikungunya Virus: Structures, Syntheses, and Isolation from Natural Sources
inferred← citeshttps://doi.org/10.1007/978-981-15-1761-7_14openalex-snapshot
Bioactive Phytocompounds to Fight Against Antimicrobial Resistance
inferred← citeshttps://doi.org/10.1007/s00210-023-02517-2openalex-snapshot
Role of phytocompounds as the potential anti-viral agent: an overview
inferred← citeshttps://doi.org/10.1007/s11101-020-09667-8openalex-snapshot
Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
inferred← citeshttps://doi.org/10.1007/s11418-015-0910-zopenalex-snapshot
Chikungunya virus (CHIKV) inhibitors from natural sources: a medicinal chemistry perspective
inferred← citeshttps://doi.org/10.1016/b978-0-12-817905-5.00009-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91814-5.00011-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.apsb.2018.03.011openalex-snapshot
Helioscopianoids A–Q, bioactive jatrophane diterpenoid esters from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103763openalex-snapshot
Euphoresulanes A–M, structurally diverse jatrophane diterpenoids from Euphorbia esula
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117366openalex-snapshot
Daphnanes diterpenes from the latex of Hura crepitans L. and their PKCζ-dependent anti-proliferative activity on colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.09.092openalex-snapshot
Insights on profiling of phorbol, deoxyphorbol, ingenol and jatrophane diterpene esters by high performance liquid chromatography coupled to multiple stage mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.03.007openalex-snapshot
Polypharmacology in HIV inhibition: can a drug with simultaneous action against two relevant targets be an alternative to combination therapy?
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.06.021openalex-snapshot
LC-MS2-Based dereplication of Euphorbia extracts with anti-Chikungunya virus activity
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115574openalex-snapshot
Phytochemical and pharmacological review of diterpenoids from the genus Euphorbia Linn (2012–2021)
inferred← citeshttps://doi.org/10.1016/j.nexres.2025.100140openalex-snapshot
An assessment of the antiviral compounds found in ethnomedicinal plants
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.12.021openalex-snapshot
Chemical profile and defensive function of the latex of Euphorbia peplus
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.01.016openalex-snapshot
Jatrophane diterpenoids with multidrug-resistance modulating activity from the latex of Euphorbia nicaeensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113420openalex-snapshot
Jatrophane diterpenoids with cytotoxic activity from the whole plant of Euphorbia heliosocpia L
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.04.023openalex-snapshot
Tonantzitlolones from Stillingia lineata ssp. lineata as potential inhibitors of chikungunya virus
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.007openalex-snapshot
Jatrophane diterpenes from Euphorbia guyoniana are new potent inhibitors of atrial GIRK channels
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00073openalex-snapshot
Antiviral Activity of Diterpene Esters on Chikungunya Virus and HIV Replication
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00116openalex-snapshot
Antiviral Activity of Flexibilane and Tigliane Diterpenoids from Stillingia lineata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00511openalex-snapshot
Advanced Structural Determination of Diterpene Esters Using Molecular Modeling and NMR Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01016openalex-snapshot
Simplified Bryostatin Analogues Protect Cells from Chikungunya Virus-Induced Cell Death
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00644openalex-snapshot
Euphorbia dendroides Latex as a Source of Jatrophane Esters: Isolation, Structural Analysis, Conformational Study, and Anti-CHIKV Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00990openalex-snapshot
Evaluation of Jatrophane Esters from Euphorbia spp. as Modulators of Candida albicans Multidrug Transporters
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00113openalex-snapshot
Environmentally Friendly Procedure Based on Supercritical Fluid Chromatography and Tandem Mass Spectrometry Molecular Networking for the Discovery of Potent Antiviral Compounds from Euphorbia semiperfoliata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00233openalex-snapshot
Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00500openalex-snapshot
Diterpenoids from Euphorbia dulcis with Potassium Ion Channel Inhibitory Activity with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effect
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00800openalex-snapshot
Antiviral Compounds from Codiaeum peltatum Targeted by a Multi-informative Molecular Networks Approach
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01087openalex-snapshot
Studies of Jatrogossone A as a Reactive Oxygen Species Inducer in Cancer Cellular Models
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04145openalex-snapshot
Diterpenoids with Rearranged 9(10→11)-abeo-10,12-Cyclojatrophane Skeleton and the First (15S)-Jatrophane from Euphorbia helioscopia: Structural Elucidation, Biomimetic Conversion, and Their Immunosuppressive Effects
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00787openalex-snapshot
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus
inferred← citeshttps://doi.org/10.1021/acsinfecdis.7b00219openalex-snapshot
Inhibition of the Replication of Different Strains of Chikungunya Virus by 3-Aryl-[1,2,3]triazolo[4,5-d]pyrimidin-7(6H)-ones
inferred← citeshttps://doi.org/10.1021/acsomega.0c06191openalex-snapshot
1,3-Thiazolbenzamide Derivatives as Chikungunya Virus nsP2 Protease Inhibitors
inferred← citeshttps://doi.org/10.1038/s41598-017-04399-wopenalex-snapshot
Heliosterpenoids A and B, two Novel Jatrophane-Derived Diterpenoids with a 5/6/4/6 Ring System from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1039/c5np00087dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.1055/a-0589-0525openalex-snapshot
Bioactive Segetane, Ingenane, and Jatrophane Diterpenes from Euphorbia taurinensis
inferred← citeshttps://doi.org/10.1080/07391102.2021.1904004openalex-snapshot
A review targeting the infection by CHIKV using computational and experimental approaches
inferred← citeshttps://doi.org/10.1080/14787210.2019.1595591openalex-snapshot
Spectrum of candidate molecules against Chikungunya virus - an insight into the antiviral screening platforms
inferred← citeshttps://doi.org/10.1089/act.2016.29062.eyaopenalex-snapshot
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inferred← citeshttps://doi.org/10.1107/s205698901901541xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1128/cmr.00348-20openalex-snapshot
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inferred← citeshttps://doi.org/10.1177/1934578x19848168openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12992-023-00906-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s13071-022-05367-8openalex-snapshot
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inferred← citeshttps://doi.org/10.12662/2317-3076jhbs.v10i1.4237.p1-10.2022openalex-snapshot
Study of the interactions of di- and tri-terpenes from Stillingia loranthacea with the enzyme NSP16-NSP10 of SARS-CoV-2
inferred← citeshttps://doi.org/10.14805/jphchem.2014.art22openalex-snapshot
Chikungunya epidemiological survey and Current available inhibitors
inferred← citeshttps://doi.org/10.2217/fvl-2022-0163openalex-snapshot
In Silico Assessment of Diterpenes as Potential Inhibitors of SARS-COV-2 Main Protease
inferred← citeshttps://doi.org/10.31254/phyto.2020.9412openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpubh.2020.618624openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules24122336openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ph14070653openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants9080958openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/v10050235openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/v16020218openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/v16121929openalex-snapshot
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inferred← citeshttps://doi.org/10.4103/0972-9062.263719openalex-snapshot
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inferred← citeshttps://doi.org/10.57634/rcr5056openalex-snapshot
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inferred← citeshttps://doi.org/10.6084/m9.figshare.20625097openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/f9f211c7zf244z4823zbf9az25e9adfe4295openalex-snapshot
Nouvelle stratégie de priorisation pour l’étude des produits naturels par l’approche des réseaux moléculaires multi-informatifs
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