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Structural Modifications of the Antiinflammatory Oxicam Scaffold and Preparation of Anticancer Organometallic Compounds

https://doi.org/10.1021/acs.organomet.8b00751
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Association of Analgesic Use With Risk of Ovarian Cancer in the Nurses’ Health Studies
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The Prodrug Platin‐A: Simultaneous Release of Cisplatin and Aspirin
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Half‐Sandwich Ruthenium(II) Biotin Conjugates as Biological Vectors to Cancer Cells
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Anti‐Inflammatory Oxicams as Multi‐donor Ligand Systems: pH‐ and Solvent‐Dependent Coordination Modes of Meloxicam and Piroxicam to Ru and Os
inferredcites →https://doi.org/10.1002/cplu.201402390openalex-snapshot
Organoruthenium and Osmium Anticancer Complexes Bearing a Maleimide Functional Group: Reactivity to Cysteine, Stability, and Cytotoxicity
inferredcites →https://doi.org/10.1002/cplu.201700050openalex-snapshot
Functionalization of Ruthenium(II)(η6‐p‐cymene)(3‐hydroxy‐2‐pyridone) Complexes with (Thio)Morpholine: Synthesis and Bioanalytical Studies
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RuII(η6‐p‐cymene) Complexes of Bioactive 1,2‐Benzothiazines: Protein Binding vs. Antitumor Activity
inferredcites →https://doi.org/10.1002/iub.1334openalex-snapshot
Oxicams, a class of nonsteroidal anti‐inflammatory drugs and beyond
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Prediction of the interaction of metallic moieties with proteins: An update for protein‐ligand docking techniques
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3‐Oxo‐1,2‐benzoisothiazoline‐2‐acetic acid 1,1‐dioxide derivatives. I. Reaction of esters with alkoxides
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Piroxicam and other anti‐inflammatory oxicams
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Improved protein–ligand docking using GOLD
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General and targeted statistical potentials for protein–ligand interactions
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Development and validation of a genetic algorithm for flexible docking 1 1Edited by F. E. Cohen
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Carbonyl-η-hexamethylbenzene complexes of osmium. Carbon-hydrogen activation by (η-C6Me6)Os(CO)(H)2
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Structure and physicochemical properties of meloxicam, a new NSAID
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Cyclooxygenases in cancer: progress and perspective
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Arene ruthenium and pentamethylcyclopentadienyl rhodium and iridium complexes containing N,O-chelating ligands derived from piroxicam: Synthesis, molecular structure and cytotoxicity
inferredcites →https://doi.org/10.1016/j.jinorgbio.2016.06.025openalex-snapshot
Anticancer activity of Ru- and Os(arene) compounds of a maleimide-functionalized bioactive pyridinecarbothioamide ligand
inferredcites →https://doi.org/10.1016/j.jorganchem.2012.10.042openalex-snapshot
Solution equilibrium studies on anticancer ruthenium(II)–η6-p-cymene complexes of 3-hydroxy-2(1H)-pyridones
inferredcites →https://doi.org/10.1016/s0140-6736(10)62110-1openalex-snapshot
Effect of daily aspirin on long-term risk of death due to cancer: analysis of individual patient data from randomised trials
inferredcites →https://doi.org/10.1021/acs.inorgchem.5b02690openalex-snapshot
Nonsteroidal Anti-inflammatory—Organometallic Anticancer Compounds
inferredcites →https://doi.org/10.1021/ci800298zopenalex-snapshot
Empirical Scoring Functions for Advanced Protein−Ligand Docking with PLANTS
inferredcites →https://doi.org/10.1021/ja00467a001openalex-snapshot
Conformational analysis. 130. MM2. A hydrocarbon force field utilizing V1 and V2 torsional terms
inferredcites →https://doi.org/10.1021/jm00263a017openalex-snapshot
Potent antiinflammatory N-heterocyclic 3-carboxamides of 4-hydroxy-2-methyl-2H-1,2-benzothiazine 1,1-dioxide
inferredcites →https://doi.org/10.1021/jm00278a016openalex-snapshot
Sudoxicam and related N-heterocyclic carboxamides of 4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide. Potent nonsteroidal antiinflammatory agents
inferredcites →https://doi.org/10.1021/jm00294a008openalex-snapshot
Synthesis and antiinflammatory activity of some 3-carboxamides of 2-alkyl-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide
inferredcites →https://doi.org/10.1021/jm0613166openalex-snapshot
Structural and Functional Basis of Cyclooxygenase Inhibition
inferredcites →https://doi.org/10.1021/om500825hopenalex-snapshot
Anticancer Ruthenium(η6-p-cymene) Complexes of Nonsteroidal Anti-inflammatory Drug Derivatives
inferredcites →https://doi.org/10.1023/a:1007996124545openalex-snapshot
Empirical scoring functions: I. The development of a fast empirical scoring function to estimate the binding affinity of ligands in receptor complexes
inferredcites →https://doi.org/10.1038/bjc.2014.271openalex-snapshot
Molecular targets of aspirin and cancer prevention
inferredcites →https://doi.org/10.1038/nsb1203-980openalex-snapshot
Announcing the worldwide Protein Data Bank
inferredcites →https://doi.org/10.1039/c7cs00332copenalex-snapshot
Structure–activity relationships for ruthenium and osmium anticancer agents – towards clinical development
inferredcites →https://doi.org/10.1039/dt9740000233openalex-snapshot
Arene ruthenium(II) complexes formed by dehydrogenation of cyclohexadienes with ruthenium(III) trichloride
inferredcites →https://doi.org/10.1056/nejmoa1207756openalex-snapshot
Aspirin Use, Tumor PIK3CA Mutation, and Colorectal-Cancer Survival
inferredcites →https://doi.org/10.1074/jbc.m113.517987openalex-snapshot
Oxicams Bind in a Novel Mode to the Cyclooxygenase Active Site via a Two-water-mediated H-bonding Network
inferredcites →https://doi.org/10.1093/nar/28.1.235openalex-snapshot
The Protein Data Bank
inferredcites →https://doi.org/10.1107/s0108767307043930openalex-snapshot
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inferredcites →https://doi.org/10.1124/dmd.30.2.161openalex-snapshot
Conjugation of Desmethylnaproxen in the Rat—A Novel Acyl Glucuronide-Sulfate Diconjugate as a Major Biliary Metabolite
inferredcites →https://doi.org/10.1126/science.337.6101.1471openalex-snapshot
Will an Aspirin a Day Keep Cancer Away?
inferredcites →https://doi.org/10.7326/0003-4819-159-2-201307160-00002openalex-snapshot
Alternate-Day, Low-Dose Aspirin and Cancer Risk: Long-Term Observational Follow-up of a Randomized Trial

What points at this work

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

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inferred← citeshttps://doi.org/10.1007/s00775-020-01760-9openalex-snapshot
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New Ru(II)-p-cymene compounds bearing indomethacin and indomethacin-pyridineamide ligands: synthesis, characterization, computational studies and investigation of their interactions with the Human Serum Albumin
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