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Anti-HIV Tigliane Diterpenoids from Wikstroemia scytophylla
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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/cbdv.201600040openalex-snapshot
Chemical Constituents from the Stems of Daphne holosericea ( Diels ) Hamaya
inferredcites →https://doi.org/10.1002/cjoc.201200011openalex-snapshot
A New Guaiane‐type Sesquiterpene with 15 Known Compounds from Wikstroemia scytophylla Diels
inferredcites →https://doi.org/10.1002/ijch.197600010openalex-snapshot
Chiroptical Properties of Phorbol‐12, 13, 20‐triacetate and Some Other Phorbol Derivatives
inferredcites →https://doi.org/10.1002/ptr.2650070220openalex-snapshot
Oligo‐ and macrocyclic diterpenes in thymelaeaceae and euphorbiaceae occurring and utilized in yunnan (Southwest China) 4. Tigliane type diterpene esters (phorbol–12,13‐diesters) from Wikstroemia canescens
inferredcites →https://doi.org/10.1007/s10600-012-0318-xopenalex-snapshot
A new tigliane-type diterpene ester from Wikstroemia scytophylla
inferredcites →https://doi.org/10.1016/0040-4020(82)85040-0openalex-snapshot
Circular dichroism and stereochemistry of chiral conjugated cyclohexenones
inferredcites →https://doi.org/10.1016/j.fitote.2015.09.017openalex-snapshot
Three new 1α-alkyldaphnane-type diterpenoids from the flower buds of Wikstroemia chamaedaphne
inferredcites →https://doi.org/10.1016/j.phytochem.2018.01.021openalex-snapshot
Diterpenes from buds of Wikstroemia chamaedaphne showing anti-hepatitis B virus activities
inferredcites →https://doi.org/10.1016/j.phytochem.2020.112360openalex-snapshot
Anti-HIV tigliane diterpenoids from Reutealis trisperma
inferredcites →https://doi.org/10.1016/s0031-9422(97)00529-3openalex-snapshot
Minor daphnane-type diterpenoids from Wikstroemia retusa
inferredcites →https://doi.org/10.1021/acs.orglett.9b03539openalex-snapshot
Daphneodorins A–C, Anti-HIV Gnidimacrin Related Macrocyclic Daphnane Orthoesters from Daphne odora
inferredcites →https://doi.org/10.1021/cr200397nopenalex-snapshot
Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families
inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferredcites →https://doi.org/10.1021/np300815topenalex-snapshot
Isolation, Structure Determination, and Anti-HIV Evaluation of Tigliane-Type Diterpenes and Biflavonoid from Stellera chamaejasme
inferredcites →https://doi.org/10.1021/ol200889sopenalex-snapshot
Stelleralides A–C, Novel Potent Anti-HIV Daphnane-Type Diterpenoids from Stellera chamaejasme L.
inferredcites →https://doi.org/10.1111/jvim.15806openalex-snapshot
Randomized controlled clinical study evaluating the efficacy and safety of intratumoral treatment of canine mast cell tumors with tigilanol tiglate (EBC-46)
inferredcites →https://doi.org/10.1182/blood.v98.10.3006openalex-snapshot
Prostratin: activation of latent HIV-1 expression suggests a potential inductive adjuvant therapy for HAART
inferredcites →https://doi.org/10.3389/fvets.2019.00106openalex-snapshot
Dose Characterization of the Investigational Anticancer Drug Tigilanol Tiglate (EBC-46) in the Local Treatment of Canine Mast Cell Tumors
inferredcites →https://doi.org/10.4103/pm.pm_275_16openalex-snapshot
Flavones and lignans from the stems of Wikstroemia scytophylla diels
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.2022.113475zenodo-depositor-declared
Fungal polyketides from a rhizospheric soil-derived Penicillium sp. YUD17004 associated with Gastrodia elata
inferred← citeshttps://doi.org/10.1007/s11418-022-01621-6openalex-snapshot
A feruloylated acylglycerol isolated from Wikstroemia pilosa and its distribution in ten plants of Wikstroemia species
inferred← citeshttps://doi.org/10.1007/s11418-023-01713-xopenalex-snapshot
Tigliane and daphnane diterpenoids from Thymelaeaceae family: chemistry, biological activity, and potential in drug discovery
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128319openalex-snapshot
New phorbol ester derivatives as potent anti-HIV agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115726openalex-snapshot
Natural products as potential lead compounds to develop new antiviral drugs over the past decade
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105731openalex-snapshot
LC-MS identification, isolation, and structural elucidation of anti-HIV macrocyclic daphnane orthoesters from Edgeworthia chrysantha
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113468openalex-snapshot
Targeted isolation of diterpenoids and sesquiterpenoids from Daphne gemmata E. Pritz. ex Diels using molecular networking together with network annotation propagation and MS2LDA
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.03.003openalex-snapshot
Bioactive constituents from the leaves of Croton tiglium
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.08.003openalex-snapshot
Tigliane diterpenoids with cytotoxic activities from Croton damayeshu
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00570openalex-snapshot
LC-MS Identification, Isolation, and Structural Elucidation of Anti-HIV Tigliane Diterpenoids from Wikstroemia lamatsoensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00977openalex-snapshot
Tigliane Diterpenoids with Larvicidal, Antifungal, and α-Glucosidase Inhibitory Activities from Croton damayeshu
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01195openalex-snapshot
Anti-HIV Tigliane-Type Diterpenoids from the Aerial Parts of Wikstroemia lichiangensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00894openalex-snapshot
Daphnepedunins A–F, Anti-HIV Macrocyclic Daphnane Orthoester Diterpenoids from Daphne pedunculata
inferred← citeshttps://doi.org/10.1021/jacs.4c01589openalex-snapshot
Total Syntheses of Phorbol and 11 Tigliane Diterpenoids and Their Evaluation as HIV Latency-Reversing Agents
inferred← citeshttps://doi.org/10.1039/d0np00086hopenalex-snapshot
Balancing skeleton and functional groups in total syntheses of complex natural products: a case study of tigliane, daphnane and ingenane diterpenoids
inferred← citeshttps://doi.org/10.1039/d4ra08447kopenalex-snapshot
Genome mining of albocandins A–E from Streptomyces sp. YINM00030
inferred← citeshttps://doi.org/10.1080/14786419.2023.2209821openalex-snapshot
Chemical constituents of Wikstroemia alternifolia and their neuroprotective activities
inferred← citeshttps://doi.org/10.2174/1389201024666230606122116openalex-snapshot
Wikstroemia: A Review on its Phytochemistry and Pharmacology
inferred← citeshttps://doi.org/10.3390/molecules27238280openalex-snapshot
Lead/Drug Discovery from Natural Resources
inferred← citeshttps://doi.org/10.3390/molecules30071452openalex-snapshot
Anti-HIV Activity of Tigliane Derivatives from Euphorbia nicaeensis Roots
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