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Cytotoxic Clerodane Diterpenes from Zuelania guidonia

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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.200800342openalex-snapshot

Casearin X, Its Degradation Product and Other Clerodane Diterpenes from Leaves of Casearia sylvestris: Evaluation of Cytotoxicity against Normal and Tumor Human Cells

inferredcites →https://doi.org/10.1002/cbdv.200890007openalex-snapshot

New Bioactive Clerodane Diterpenoids from the Roots of Casearia membranacea

inferredcites →https://doi.org/10.1002/hlca.200900031openalex-snapshot

Clerodane and ent‐Kaurane Diterpene Glycosyl and Glycoside Derivatives from the Leaves of Casearia sylvestris

inferredcites →https://doi.org/10.1016/0031-9422(90)80131-yopenalex-snapshot

Diterpenes from Zuelania guidonia

inferredcites →https://doi.org/10.1016/0031-9422(90)87110-gopenalex-snapshot

Clerodane diterpenes from Zuelania guidonia stem bark

inferredcites →https://doi.org/10.1016/0031-9422(95)00623-0openalex-snapshot

Clerodane diterpenes from the bark of Casearia tremula

inferredcites →https://doi.org/10.1016/0031-9422(96)00147-1openalex-snapshot

Amarisolide, a neo-clerodane diterpene glycoside from Salvia amarissima

inferredcites →https://doi.org/10.1016/j.biortech.2009.01.001openalex-snapshot

Pleurotus species convert monoterpenes to furanoterpenoids through 1,4-endoperoxides

inferredcites →https://doi.org/10.1016/j.bmc.2011.06.067openalex-snapshot

In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica

inferredcites →https://doi.org/10.1016/j.bse.2007.03.003openalex-snapshot

Clerodane diterpenes from the stems of Casearia grewiifolia var. gelonioides (Flacourtiaceae/Salicaceae sensu lato)

inferredcites →https://doi.org/10.1016/j.cbi.2010.08.008openalex-snapshot

Casearin X exhibits cytotoxic effects in leukemia cells triggered by apoptosis

inferredcites →https://doi.org/10.1016/s0031-9422(00)00281-8openalex-snapshot

Cytotoxic clerodane diterpene esters from Laetia corymbulosa

inferredcites →https://doi.org/10.1016/s0031-9422(00)83754-1openalex-snapshot

Diterpene glycosides and other constituents from argentinian baccharis species

inferredcites →https://doi.org/10.1016/s0031-9422(02)00064-xopenalex-snapshot

Clerodane and labdane diterpene glycosides from a Malagasy endemic plant, Cussonia racemosa

inferredcites →https://doi.org/10.1016/s0031-9422(02)00437-5openalex-snapshot

Clerodane diterpenes from Baccharis sagittalis : insect antifeedant activity

inferredcites →https://doi.org/10.1016/s0031-9422(97)00377-4openalex-snapshot

Biologically active clerodane-type diterpene glycosides from the root-stalks of Dicranopteris pedata

inferredcites →https://doi.org/10.1021/jo030330copenalex-snapshot

Triphenylphosphine-Induced Ring Contraction of 1,2-Dioxines

inferredcites →https://doi.org/10.1021/jo900669uopenalex-snapshot

Dihydroxylation of 4-Substituted 1,2-Dioxines: A Concise Route to Branched Erythro Sugars

inferredcites →https://doi.org/10.1021/np010405copenalex-snapshot

Structure and Stereochemistry of New Cytotoxic Clerodane Diterpenoids from the Bark of Casearia lucida from the Madagascar Rainforest

inferredcites →https://doi.org/10.1021/np010459mopenalex-snapshot

Novel Bioactive Clerodane Diterpenoids from the Leaves and Twigs of Casearia sylvestris

inferredcites →https://doi.org/10.1021/np0303658openalex-snapshot

New Cytotoxic Clerodane Diterpenoids from the Leaves and Twigs of Casearia membranacea

inferredcites →https://doi.org/10.1021/np049757kopenalex-snapshot

New Bioactive Clerodane Diterpenoids from the Bark of Casearia grewiifolia

inferredcites →https://doi.org/10.1021/np058063oopenalex-snapshot

Cytotoxic Clerodane Diterpenoids from Casearia membranacea

inferredcites →https://doi.org/10.1021/np0603166openalex-snapshot

Tetranorclerodanes and Clerodane-Type Diterpene Glycosides from Dicranopteris dichotoma

inferredcites →https://doi.org/10.1021/np0605034openalex-snapshot

Cytotoxic Clerodane Diterpenoids and Their Hydrolysis Products from Casearia nigrescens from the Rainforest of Madagascar

inferredcites →https://doi.org/10.1021/np070083yopenalex-snapshot

Cytotoxic Clerodane Diterpenoids from Fruits of Casearia grewiifolia

inferredcites →https://doi.org/10.1021/np070367iopenalex-snapshot

Structure and Absolute Configuration of Clerodane Diterpene Glycosides and a Rearranged Cadinane Sesquiterpene Glycoside from the Stems of Tinospora sinensis

inferredcites →https://doi.org/10.1021/np1004455openalex-snapshot

Clerodane Diterpenes from Casearia arguta That Act As Synergistic TRAIL Sensitizers

inferredcites →https://doi.org/10.1021/np100620xopenalex-snapshot

Configurational Assignment of Cyclic Peroxy Metabolites Provides an Insight into Their Biosynthesis: Isolation of Plakortolides, seco-Plakortolides, and Plakortones from the Australian Marine Sponge Plakinastrella clathrata

inferredcites →https://doi.org/10.1021/np100840wopenalex-snapshot

Cytotoxic Clerodane Diterpenes from Casearia rupestris

inferredcites →https://doi.org/10.1021/np9004079openalex-snapshot

Cytotoxic Clerodane Diterpenoids from Casearia obliqua

inferredcites →https://doi.org/10.1021/np990553ropenalex-snapshot

Novel Cytotoxic Diterpenes from Casearia arborea

inferredcites →https://doi.org/10.1021/ol300657hopenalex-snapshot

Cordifolide A, a Sulfur-Containing Clerodane Diterpene Glycoside from Tinospora cordifolia

inferredcites →https://doi.org/10.1039/p19920000781openalex-snapshot

Biologically active clerodane-type diterpene alcohol and its glycosides from the root-stalks of ferns

inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot

An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II

inferredcites →https://doi.org/10.1055/s-0031-1280163openalex-snapshot

Clerodane Diterpenoids fromTinospora sagittata(Oliv.) Gagnep

inferredcites →https://doi.org/10.1071/c97183openalex-snapshot

Two New Clerodane Glycosides from Gleichenia microphylla

inferredcites →https://doi.org/10.1139/v75-168openalex-snapshot

Further Studies on the Assignment of Signals in 13C Magnetic Resonance Spectra of Aldoses and Derived Methyl Glycosides

inferredcites →https://doi.org/10.1248/cpb.36.1585openalex-snapshot

Antitumor principles from Casearia sylvestris Sw.(Flacourtiaceae). Structure elucidation of new clerodane diterpenes by 2-D NMR spectroscopy.

inferredcites →https://doi.org/10.1248/cpb.38.3384openalex-snapshot

New antitumor principles, casearins A-F, for Casearia sylvestris Sw. (Flacourtiaceae).

inferredcites →https://doi.org/10.1248/cpb.39.693openalex-snapshot

Structures and cytotoxic activity relationship of casearins, new clerodane diterpenes from Caseariasylvestris Sw.

inferredcites →https://doi.org/10.1248/cpb.52.108openalex-snapshot

Two New Cytotoxic Clerodane Diterpenoids from Casearia membranacea

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4484092openalex-extracted

Bioactive Diterpenoids Isolated From the Twigs and Leaves of Casaeria Balansea

inferred← citeshttps://doi.org/10.1002/ajoc.202200668openalex-snapshot

Robinson Annulation Applied to the Total Synthesis of Natural Products

inferred← citeshttps://doi.org/10.1002/asia.201900368openalex-snapshot

Diastereoselective Total Syntheses of (±)‐Caseabalansin A and (±)‐18‐Epicaseabalansin A via Intramolecular Robinson‐type Annulation

inferred← citeshttps://doi.org/10.1002/vjch.202000014openalex-snapshot

Mini Review: Anticancer activity of diterpenoid peroxides

inferred← citeshttps://doi.org/10.1007/s12551-022-00946-6openalex-snapshot

Solid-state NMR and hyperpolarization methods for the Research, Development, and Innovation in Costa Rican science

inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107890openalex-snapshot

Butanolides and clerodane diterpenes from the twigs of Casearia grewiifolia and their effects on adiponectin secretion

inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105654openalex-snapshot

Bioactive diterpenoids isolated from the twigs and leaves of Casearia velutina

inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106116openalex-snapshot

Pediatric acute lymphoblastic leukemia management using multitargeting bioactive natural compounds: A systematic and critical review

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113802openalex-snapshot

Labdane and ent-halimane diterpenoids with STAT3-inhibitory activity from Leonurus sibiricus

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113864openalex-snapshot

Stereochemical assignment of clerodane-type diterpenes from the fruits of Casearia grewiifolia and their ability to inhibit PCSK9 expression

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151892openalex-snapshot

Cyclic dipeptides with peroxy groups from the fruiting bodies of the edible mushroom Tricholoma matsutake

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b01509openalex-snapshot

Sarco/Endoplasmic Reticulum Calcium ATPase Inhibitors: Beyond Anticancer Perspective

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00062openalex-snapshot

Discovery of Tricyclic Clerodane Diterpenes as Sarco/Endoplasmic Reticulum Ca2+-ATPase Inhibitors and Structure–Activity Relationships

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00583openalex-snapshot

Characterization and Biological Evaluation of Diterpenoids from Casearia graveolens

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00224openalex-snapshot

Modified Cytotoxic Terpenoids from the Tuber of Icacina trichantha

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00233openalex-snapshot

Bifunctional Duocarmycin Analogues as Inhibitors of Protein Tyrosine Kinases

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01015openalex-snapshot

Anacolosins A–F and Corymbulosins X and Y, Clerodane Diterpenes from Anacolosa clarkii Exhibiting Cytotoxicity toward Pediatric Cancer Cell Lines

inferred← citeshttps://doi.org/10.1021/acs.joc.7b02951openalex-snapshot

Corymbulosins I–W, Cytotoxic Clerodane Diterpenes from the Bark of Laetia corymbulosa

inferred← citeshttps://doi.org/10.1021/ol502129uopenalex-snapshot

Total Synthesis of (−)-Bucidarasin A Starting from an Original Chiral Building Block

inferred← citeshttps://doi.org/10.1038/cddis.2015.413openalex-snapshot

The clerodane diterpene casearin J induces apoptosis of T-ALL cells through SERCA inhibition, oxidative stress, and interference with Notch1 signaling

inferred← citeshttps://doi.org/10.1039/c5np00087dopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/c5np00137dopenalex-snapshot

Clerodane diterpenes: sources, structures, and biological activities

inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.18845/tm.v37i3.6870openalex-snapshot

Resonancia Magnética Nuclear en Costa Rica: una perspectiva histórica

inferred← citeshttps://doi.org/10.3389/fmicb.2017.00221openalex-snapshot

Wide Distribution of Foxicin Biosynthetic Gene Clusters in Streptomyces Strains – An Unusual Secondary Metabolite with Various Properties

inferred← citeshttps://doi.org/10.3390/compounds6010007openalex-snapshot

Endoperoxides: Highly Oxygenated Terpenoids with Anticancer and Antiprotozoal Activities

inferred← citeshttps://doi.org/10.3390/molecules23020410openalex-snapshot

Ent-Clerodane Diterpenes from the Bark of Croton oligandrus Pierre ex Hutch. and Assessment of Their Cytotoxicity against Human Cancer Cell Lines

inferred← citeshttps://doi.org/10.3390/molecules25102288openalex-snapshot

Clerodane Diterpenoids from Callicarpa hypoleucophylla and Their Anti-Inflammatory Activity

inferred← citeshttps://doi.org/10.3987/com-14-13161openalex-snapshot

Enantioselective Total Synthesis of (+)-Bucidarasins A and C

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