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The 65 checked references that resolve
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resolves10.1002/tcr.1008Chemistry and chemical biology of taxane anticancer agents
resolves10.1021/jm9604080Syntheses and Structure−Activity Relationships of the Second-Generation Antitumor Taxoids: Exceptional Activity against Drug-Resistant Cancer Cells
resolves10.1021/jm960505tButitaxel Analogues: Synthesis and Structure−Activity Relationships
resolves10.1021/jm980229dSynthesis and Biological Evaluation of 2-Acyl Analogues of Paclitaxel (Taxol)
resolves10.1021/jm0102607Synthesis and Antitumor Activity of Novel C-7 Paclitaxel Ethers: Discovery of BMS-184476
resolves10.1021/jm049483yDesign, Synthesis and Structure−Activity Relationships of Novel Taxane-Based Multidrug Resistance Reversal Agents
resolves10.1021/jm800086eDesign, Synthesis, and Biological Evaluation of New-Generation Taxoids
resolves10.1271/bbb.110797Relationship between the Structures of Taxane Derivatives and Their Microtubule Polymerization Activity
resolves10.1021/jm401708fSilicate Esters of Paclitaxel and Docetaxel: Synthesis, Hydrophobicity, Hydrolytic Stability, Cytotoxicity, and Prodrug Potential
resolves10.1016/S0968-0896(02)00218-3Structure–activity relationship study at the 3′-N-position of paclitaxel: synthesis and biological evaluation of 3′-N-acyl-paclitaxel analogues
resolves10.1016/j.bmcl.2005.10.089Syntheses and evaluation of novel fatty acid-second-generation taxoid conjugates as promising anticancer agents
resolves10.1007/s11178-005-0168-0Taxol: Synthesis, Bioactive Conformations, and Structure-Activity Relationships in Its Analogs
resolves10.1002/cplu.201402390Organoruthenium and Osmium Anticancer Complexes Bearing a Maleimide Functional Group: Reactivity to Cysteine, Stability, and Cytotoxicity
resolves10.1021/cb4000844Analysis of the Mechanism of Action of Potent Antibacterial Hetero-tri-organometallic Compounds: A Structurally New Class of Antibiotics
resolves10.1007/s11164-013-1489-1Synthesis, characterization, and antimicrobial activity of novel heterocyclic compounds containing a ferrocene unit via Michael addition reaction
resolves10.1002/aoc.1691Ferrocene‐modified thiopyrimidines: synthesis, enantiomeric resolution, antitumor activity
resolves10.1016/j.ejmech.2009.01.029Synthesis, characterization and in vitro antiproliferative activities of new 13-cis-retinoyl ferrocene derivatives
resolves10.1021/jm900297xA [3]Ferrocenophane Polyphenol Showing a Remarkable Antiproliferative Activity on Breast and Prostate Cancer Cell Lines
resolves10.1039/CC9960000955Ferrocenyl hydroxytamoxifen: a prototype for a new range of oestradiol receptor site-directed cytotoxics
resolves10.1016/S0022-328X(97)00086-7Facile route to ferrocifen, 1-[4-(2-dimethylaminoethoxy)]-1-(phenyl-2-ferrocenyl-but-1-ene), first organometallic analogue of tamoxifen, by the McMurry reaction
resolves10.1039/c0dt00169dOrganometallic cyclic polyphenols derived from 1,2-(α-keto tri or tetra methylene) ferrocene show strong antiproliferative activity on hormone-independent breast cancer cells
resolves10.1016/j.jorganchem.2012.05.042Synthesis, electrochemistry and anticancer activity of novel ferrocenyl phenols prepared via azide-alkyne 1,3-cycloaddition reaction
resolves10.1021/jm060259dProbing the Role of the Covalent Linkage of Ferrocene into a Chloroquine Template
resolves10.1021/jm901357nEnhancement of the Antimalarial Activity of Ciprofloxacin Using a Double Prodrug/Bioorganometallic Approach
resolves10.1021/jm301077mFerrocenyl Derivatives of the Anthelmintic Praziquantel: Design, Synthesis, and Biological Evaluation
resolves10.1039/C5CC00904AAntibacterial properties and atomic resolution X-ray complex crystal structure of a ruthenocene conjugated β-lactam antibiotic
resolves10.1039/c0md00231cSynthesis and biological evaluation of novel ferrocenyl curcuminoid derivatives
resolves10.1039/c2md00315eSynthesis and biological activities of ferrocenyl derivatives of paclitaxel
resolves10.1021/acsmedchemlett.6b00046Ferrocenyl 2,5-Piperazinediones as Tubulin-Binding Organometallic ABCB<sub>1</sub> and ABCG<sub>2</sub> Inhibitors Active against MDR Cells
resolves10.1021/jo951961cSynthesis, Conformational Analysis, and Biological Evaluation of Heteroaromatic Taxanes
resolves10.1021/ja000293wMacrocycle Formation by Ring-Closing Metathesis. Application to the Syntheses of Novel Macrocyclic Taxoids
resolves10.1039/b921237jTotal synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin
resolves10.1016/j.ejmech.2015.05.014Preparation and biodistribution of 1-((2-methoxyphenyl) piperazine)ferrocenecarboxamide labeled with technetium-99m as a potential brain receptor imaging agent
resolves10.1021/np50056a017Modified Taxols, 4. Synthesis and Biological Activity of Taxols Modified in the Side Chain
resolves10.1016/j.bmcl.2008.09.103Paclitaxel succinate analogs: Anionic and amide introduction as a strategy to impart blood–brain barrier permeability
resolves10.1021/ja900545mAn <i>N</i>-Aroyltransferase of the BAHD Superfamily Has Broad Aroyl CoA Specificity <i>in Vitro</i> with Analogues of <i>N</i>-Dearoylpaclitaxel
resolves10.1016/0006-2952(94)90580-0Polarized transport of docetaxel and vinblastine mediated by P-glycoprotein in human intestinal epithelial cell monolayers
resolves10.1006/jmbi.1996.0897Development and validation of a genetic algorithm for flexible docking 1 1Edited by F. E. Cohen
resolves10.1002/ejic.201500770Synthesis, Characterization, and Biological Properties of Osmium‐Based Tamoxifen Derivatives – Comparison with Their Homologues in the Iron and Ruthenium Series
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