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Biological properties of jatrophane polyesters, new microtubule-interacting agents

https://doi.org/10.1007/s00280-002-0541-4
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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/cm.970280405openalex-snapshot
Rhazinilam mimics the cellular effects of taxol by different mechanisms of action
inferredcites →https://doi.org/10.1016/0003-2697(72)90094-2openalex-snapshot
Determination of protein: A modification of the lowry method that gives a linear photometric response
inferredcites →https://doi.org/10.1016/s0021-9258(17)41836-9openalex-snapshot
3'-(p-azidobenzamido)taxol photolabels the N-terminal 31 amino acids of beta-tubulin.
inferredcites →https://doi.org/10.1016/s0955-0674(98)80095-1openalex-snapshot
Microtubules and actin filaments: dynamic targets for cancer chemotherapy
inferredcites →https://doi.org/10.1016/s0960-894x(98)00226-1openalex-snapshot
New synthetic inhibitors of microtubule depolymerization
inferredcites →https://doi.org/10.1016/s0968-0896(99)00241-2openalex-snapshot
D-ring substituted rhazinilam analogues: semisynthesis and evaluation of antitubulin activity
inferredcites →https://doi.org/10.1021/bi9515127openalex-snapshot
Discodermolide, A Cytotoxic Marine Agent That Stabilizes Microtubules More Potently Than Taxol,
inferredcites →https://doi.org/10.1021/ja9717828openalex-snapshot
Eleutherobin, a New Cytotoxin that Mimics Paclitaxel (Taxol) by Stabilizing Microtubules
inferredcites →https://doi.org/10.1021/np0000872openalex-snapshot
Structure−Activity Relationship of Polyisoprenyl Benzophenones from Garcinia pyrifera on the Tubulin/Microtubule System
inferredcites →https://doi.org/10.1021/np970507wopenalex-snapshot
Macrocyclic Diterpenoids from Euphorbia semiperfoliata
inferredcites →https://doi.org/10.1038/277665a0openalex-snapshot
Promotion of microtubule assembly in vitro by taxol
inferredcites →https://doi.org/10.1073/pnas.70.3.765openalex-snapshot
Microtubule Assembly in the Absence of Added Nucleotides
inferredcites →https://doi.org/10.1073/pnas.77.3.1561openalex-snapshot
Taxol stabilizes microtubules in mouse fibroblast cells.
inferredcites →https://doi.org/10.1073/pnas.90.20.9552openalex-snapshot
Mechanism of mitotic block and inhibition of cell proliferation by taxol at low concentrations.
inferredcites →https://doi.org/10.1073/pnas.92.10.4507openalex-snapshot
Inactivation of Bcl-2 by phosphorylation.
inferredcites →https://doi.org/10.1074/jbc.272.4.2534openalex-snapshot
Activities of the Microtubule-stabilizing Agents Epothilones A and B with Purified Tubulin and in Cells Resistant to Paclitaxel (Taxol®)
inferredcites →https://doi.org/10.1097/00001813-199112000-00002openalex-snapshot
Taxol
inferredcites →https://doi.org/10.1097/00001813-199801000-00008openalex-snapshot
The potent microtubule-stabilizing agent (+)-discodermolide induces apoptosis in human breast carcinoma cells???preliminary comparisons to paclitaxel
inferredcites →https://doi.org/10.1124/mol.52.4.613openalex-snapshot
The Microtubule-Stabilizing Agent Discodermolide Competitively Inhibits the Binding of Paclitaxel (Taxol) to Tubulin Polymers, Enhances Tubulin Nucleation Reactions More Potently than Paclitaxel, and Inhibits the Growth of Paclitaxel-Resistant Cells

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.2020.112519zenodo-depositor-declared
Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone
inferred← citeshttps://doi.org/10.1002/ange.200460147openalex-snapshot
Isolation, Crystal and Solution Structure Determination, and Biosynthesis of Tubulysins—Powerful Inhibitors of Tubulin Polymerization from Myxobacteria
inferred← citeshttps://doi.org/10.1002/ange.201704929openalex-snapshot
Diastereoselective Total Synthesis of the Euphorbia Diterpenoid Pepluanol A: A Reductive Annulation Approach
inferred← citeshttps://doi.org/10.1002/ange.201915876openalex-snapshot
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System
inferred← citeshttps://doi.org/10.1002/ange.202400943openalex-snapshot
Total Synthesis of the Euphorbia Diterpenoid Pepluacetal
inferred← citeshttps://doi.org/10.1002/anie.200460147openalex-snapshot
Isolation, Crystal and Solution Structure Determination, and Biosynthesis of Tubulysins—Powerful Inhibitors of Tubulin Polymerization from Myxobacteria
inferred← citeshttps://doi.org/10.1002/anie.201704929openalex-snapshot
Diastereoselective Total Synthesis of the Euphorbia Diterpenoid Pepluanol A: A Reductive Annulation Approach
inferred← citeshttps://doi.org/10.1002/anie.201915876openalex-snapshot
Total Synthesis of (−)‐Pepluanol B: Conformational Control of the Eight‐Membered‐Ring System
inferred← citeshttps://doi.org/10.1002/anie.202400943openalex-snapshot
Total Synthesis of the Euphorbia Diterpenoid Pepluacetal
inferred← citeshttps://doi.org/10.1002/hlca.200390282openalex-snapshot
Isolation and Structure Determination of New Jatrophane Diterpenoids from Euphorbia platyphyllos L.
inferred← citeshttps://doi.org/10.1002/ptr.2334openalex-snapshot
Antileishmanial activity of piceatannol isolated from Euphorbia lagascae seeds
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Molecular and cytogenetic changes in multi-drug resistant cancer cells and their influence on new compounds testing
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Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
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Potential for cancer treatment: natural products from the Balkans
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SJ23B, a jatrophane diterpene activates classical PKCs and displays strong activity against HIV in vitro
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Apoptosis induction and modulation of P-glycoprotein mediated multidrug resistance by new macrocyclic lathyrane-type diterpenoids
inferred← citeshttps://doi.org/10.1016/j.chembiol.2004.01.014openalex-snapshot
Interaction of Epothilone Analogs with the Paclitaxel Binding Site
inferred← citeshttps://doi.org/10.1016/j.chembiol.2005.09.010openalex-snapshot
Microtubule Interactions with Chemically Diverse Stabilizing Agents: Thermodynamics of Binding to the Paclitaxel Site Predicts Cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.ejps.2012.11.012openalex-snapshot
QSAR studies of macrocyclic diterpenes with P-glycoprotein inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.fct.2011.09.035openalex-snapshot
New anti-cancer characteristics of jatrophane diterpenes from Euphorbia dendroides
inferred← citeshttps://doi.org/10.1016/j.jep.2005.05.011openalex-snapshot
Plants as a source of anti-cancer agents
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.phytol.2015.04.011openalex-snapshot
New jatrophane diterpenes from Euphorbia osyridea with proapoptotic effects on ovarian cancer cells
inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.028openalex-snapshot
New tri- and tetracyclic diterpenes from Euphorbia villosa
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.10.171openalex-snapshot
Enantioselective synthesis of the C-14 to C-5 cyclopentane segment of jatrophane diterpenes
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.046openalex-snapshot
Concise synthesis of a highly functionalized cyclopentane segment: toward the total synthesis of kansuinine A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.099openalex-snapshot
Kansuinone, a novel euphane-type triterpene from Euphorbia kansui
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00961openalex-snapshot
Enantioselective Total Synthesis of (+)-Pepluanol A
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03109openalex-snapshot
Rearrangement of the Tetra- and Tricyclic Skeletons of Pepluanol B to Access the Core Structures of Tigliane- and Myrsinane-Type Euphorbia Diterpenes
inferred← citeshttps://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferred← citeshttps://doi.org/10.1021/jacs.1c05257openalex-snapshot
Ten-Step Asymmetric Total Synthesis of (+)-Pepluanol A
inferred← citeshttps://doi.org/10.1021/jacs.6c02838openalex-snapshot
Total Synthesis of Euphopia B and Discovery of a Selective Inhibitor of Potassium Efflux-Independent NLRP3 Inflammasome Activation
inferred← citeshttps://doi.org/10.1021/jm301079zopenalex-snapshot
Microtubule Stabilizing Agents as Potential Treatment for Alzheimer’s Disease and Related Neurodegenerative Tauopathies
inferred← citeshttps://doi.org/10.1021/jo401480topenalex-snapshot
Synthesis of an Advanced Intermediate of the Jatrophane Diterpene Pl-4: A Dibromide Coupling Approach
inferred← citeshttps://doi.org/10.1021/np0400048openalex-snapshot
Bioactive Diterpenoids, a New Jatrophane and Two ent-Abietanes, and Other Constituents from Euphorbia pubescens
inferred← citeshttps://doi.org/10.1021/np200202hopenalex-snapshot
Jatrophane Diterpenes from Euphorbia esula as Antiproliferative Agents and Potent Chemosensitizers to Overcome Multidrug Resistance
inferred← citeshttps://doi.org/10.1021/np500271uopenalex-snapshot
Jatrophane Diterpenes as Inhibitors of Chikungunya Virus Replication: Structure–Activity Relationship and Discovery of a Potent Lead
inferred← citeshttps://doi.org/10.1021/ol062854fopenalex-snapshot
Lagaspholones A and B: Two New Jatropholane-Type Diterpenes from Euphorbia lagascae
inferred← citeshttps://doi.org/10.1039/b515619jopenalex-snapshot
Anticancer drugs from nature—natural products as a unique source of new microtubule-stabilizing agents
inferred← citeshttps://doi.org/10.1039/d4ra07989bopenalex-snapshot
Recent advancements in the chemistry of Diels–Alder reaction for total synthesis of natural products: a comprehensive review (2020–2023)
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Three New Jatrophane Polyesters and Antiproliferative Constituents from Euphorbia tuckeyana
inferred← citeshttps://doi.org/10.1134/s0026893316010040openalex-snapshot
RETRACTED ARTICLE: Validation of the antiproliferative effects of Euphorbia tirucalli extracts in breast cancer cell lines
inferred← citeshttps://doi.org/10.1155/2015/879238openalex-snapshot
Study on Molecular Recognition between Euphorbia Factor L713283 and β ‐Tubulin via Molecular Simulation Methods
inferred← citeshttps://doi.org/10.1177/1934578x19848168openalex-snapshot
Jatrophane Diterpenoids With Protective Effect on Human Lymphocytes DNA
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Taxol and Its Analogs
inferred← citeshttps://doi.org/10.1246/cl.2009.270openalex-snapshot
Esulatin G, a Novel Nor-diterpenoid from Euphorbia esula
inferred← citeshttps://doi.org/10.1517/13543776.16.5.647openalex-snapshot
Antitubulin agents for the treatment of cancer – a medicinal chemistry update
inferred← citeshttps://doi.org/10.2174/1381612821666151002113546openalex-snapshot
New Approaches With Natural Product Drugs for Overcoming Multidrug Resistance in Cancer
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Entropy and Enthalpy in the Activity of Tubulin-Based Antimitotic Agents
inferred← citeshttps://doi.org/10.2298/bg20130704podolskirenicopenalex-snapshot
The establishing of resistant cancer cell lines as a model for testing of new chemotherapeutics: molecular characterization of resistance developed after continuous treatment with paclitaxel
inferred← citeshttps://doi.org/10.3390/molecules30193956openalex-snapshot
Advances in the Total Synthesis of Angular Triquinane-Type Natural Products
inferred← citeshttps://doi.org/10.3390/plants9080958openalex-snapshot
So Uncommon and so Singular, but Underexplored: An Updated Overview on Ethnobotanical Uses, Biological Properties and Phytoconstituents of Sardinian Endemic Plants
inferred← citeshttps://doi.org/10.62029/jmaps.v42i1.maniopenalex-snapshot
Medicinal plant-derived therapeutics for treatment of neoplasms in modern and traditional systems of medicine
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