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Temozolomide Cocrystals with Carboxamide Coformers

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What this work says

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

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Infrared Spectroscopy: Fundamentals and Applications
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Raman Spectroscopy for Chemical Analysis
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Supramolecular Synthons in Crystal Engineering—A New Organic Synthesis
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Polymorphs and Polymorphic Cocrystals of Temozolomide
inferredcites →https://doi.org/10.1002/asia.201200205openalex-snapshot
Crystal Engineering of Stable Temozolomide Cocrystals
inferredcites →https://doi.org/10.1002/chem.201100667openalex-snapshot
A Tale of Two Polymorphic Pharmaceuticals: Pyrithyldione and Propyphenazone and their 1937 Co‐crystal Patent
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Pharmaceutical Co-Crystals
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Supramolecular Synthons and Pattern Recognition
inferredcites →https://doi.org/10.1007/s11095-006-9032-3openalex-snapshot
Use of a Glutaric Acid Cocrystal to Improve Oral Bioavailability of a Low Solubility API
inferredcites →https://doi.org/10.1007/s11095-012-0709-5openalex-snapshot
Simultaneously Improving the Mechanical Properties, Dissolution Performance, and Hygroscopicity of Ibuprofen and Flurbiprofen by Cocrystallization with Nicotinamide
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Physical stability enhancement of theophylline via cocrystallization
inferredcites →https://doi.org/10.1016/s0169-409x(01)00097-7openalex-snapshot
Crystalline solids
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Amorphous pharmaceutical solids: preparation, characterization and stabilization
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Conformational Polymorphism in Organic Crystals
inferredcites →https://doi.org/10.1021/bi00197a003openalex-snapshot
NMR and Molecular Modeling Investigation of the Mechanism of Activation of the Antitumor Drug Temozolomide and Its Interaction with DNA
inferredcites →https://doi.org/10.1021/cg034035xopenalex-snapshot
Crystal Engineering of the Composition of Pharmaceutical Phases: Multiple-Component Crystalline Solids Involving Carbamazepine
inferredcites →https://doi.org/10.1021/cg200288bopenalex-snapshot
Pyrazinamide-Diflunisal: A New Dual-Drug Co-Crystal
inferredcites →https://doi.org/10.1021/cg300784vopenalex-snapshot
Pharmaceutical Cocrystals of Niclosamide
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Polymorphism in Carbamazepine Cocrystals
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Drug Substance and Former Structure Property Relationships in 15 Diverse Pharmaceutical Co-Crystals
inferredcites →https://doi.org/10.1021/cg8005025openalex-snapshot
Effect of the Counterion on the Solubility of Isostructural Pharmaceutical Lamotrigine Salts
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Fabrication and Characterization of Te/C Nanocables and Carbonaceous Nanotubes
inferredcites →https://doi.org/10.1021/cg8007359openalex-snapshot
Co-Crystals of the Anti-HIV Drugs Lamivudine and Zidovudine
inferredcites →https://doi.org/10.1021/ja035776popenalex-snapshot
Crystal Engineering of Novel Cocrystals of a Triazole Drug with 1,4-Dicarboxylic Acids
inferredcites →https://doi.org/10.1021/ja048114oopenalex-snapshot
Crystal Engineering Approach To Forming Cocrystals of Amine Hydrochlorides with Organic Acids. Molecular Complexes of Fluoxetine Hydrochloride with Benzoic, Succinic, and Fumaric Acids
inferredcites →https://doi.org/10.1021/jm00096a013openalex-snapshot
Antitumor imidazotetrazines. 25. Crystal structure of 8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one (temozolomide) and structural comparisons with the related drugs mitozolomide and DTIC
inferredcites →https://doi.org/10.1038/bjc.1993.241openalex-snapshot
Depletion of O6-alkylguanine-DNA alkyltransferase correlates with potentiation of temozolomide and CCNU toxicity in human tumour cells
inferredcites →https://doi.org/10.1038/nrd1280openalex-snapshot
Crystal structures of drugs: advances in determination, prediction and engineering
inferredcites →https://doi.org/10.1039/b204388bopenalex-snapshot
Supramolecular synthons based on N–H⋯N and C–H⋯O hydrogen bonds. Crystal engineering of a helical structure with 5,5-diethylbarbituric acid
inferredcites →https://doi.org/10.1039/b700082kopenalex-snapshot
Supramolecular synthon polymorphism in 2 : 1 co-crystal of 4-hydroxybenzoic acid and 2,3,5,6-tetramethylpyrazine
inferredcites →https://doi.org/10.1039/b815174aopenalex-snapshot
The role of solvent in mechanochemical and sonochemical cocrystal formation: a solubility-based approach for predicting cocrystallisation outcome
inferredcites →https://doi.org/10.1039/b904616jopenalex-snapshot
Trimorphs of a pharmaceutical cocrystal involving two active pharmaceutical ingredients: potential relevance to combination drugs
inferredcites →https://doi.org/10.1039/c0cc05857bopenalex-snapshot
Synthon polymorphism and pseudopolymorphism in co-crystals. The 4,4′-bipyridine–4-hydroxybenzoic acid structural landscape
inferredcites →https://doi.org/10.1039/c0ce00214copenalex-snapshot
Cocrystals of nutraceuticalp-coumaric acid with caffeine and theophylline: polymorphism and solid-state stability explored in detail using their crystal graphs
inferredcites →https://doi.org/10.1039/c0ce00428fopenalex-snapshot
New solid forms of artemisinin obtained through cocrystallisation
inferredcites →https://doi.org/10.1039/c0ce00787kopenalex-snapshot
Highly soluble olanzapinium maleate crystalline salts
inferredcites →https://doi.org/10.1039/c0ce00842gopenalex-snapshot
Drug-drug co-crystals: Temperature-dependent proton mobility in the molecular complex of isoniazid with 4-aminosalicylic acid
inferredcites →https://doi.org/10.1039/c1ce05534hopenalex-snapshot
A hydrogen bonded cocrystal with an unusual interweaving between the adjacent triple-helices
inferredcites →https://doi.org/10.1039/c2ce26528aopenalex-snapshot
Temozolomide hydrochloride dihydrate
inferredcites →https://doi.org/10.1107/s0021889802022112openalex-snapshot
Single-crystal structure validation with the program PLATON
inferredcites →https://doi.org/10.1107/s0021889808042726openalex-snapshot
OLEX2 : a complete structure solution, refinement and analysis program
inferredcites →https://doi.org/10.1124/mol.52.2.249openalex-snapshot
Inhibition of O6-Alkylguanine DNA-Alkyltransferase or Poly(ADP-ribose) Polymerase Increases Susceptibility of Leukemic Cells to Apoptosis Induced by Temozolomide
inferredcites →https://doi.org/10.1248/yakushi.129.353openalex-snapshot
Evaluation of Stability of Temozolomide in Solutions after Opening the Capsule
inferredcites →https://doi.org/10.1524/zkri.220.4.340.61624openalex-snapshot
Crystal engineering of the composition of pharmaceutical phases. 3. Primary amide supramolecular heterosynthons and their role in the design of pharmaceutical co-crystals
inferredcites →https://doi.org/10.1557/mrs2006.206openalex-snapshot
Pharmaceutical Cocrystals: An Emerging Approach to Physical Property Enhancement
inferredcites →https://doi.org/10.2165/00024669-200201010-00006openalex-snapshot
Temozolomide
inferredcites →https://doi.org/10.5860/choice.43-0956openalex-snapshot
Modern Raman spectroscopy: a practical approach

What points at this work

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

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A Drug-Drug Cocrystal Strategy To Regulation the Stability and Solubility: A Case Study of Temozolomide/Caffeic Acid
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Simple and Efficient Synthesis of Explosive Cocrystals containing 3,5‐Dimethylpyrazol‐1‐yl‐substituted‐1,2,4,5‐tetrazines
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Exploring the cocrystallization potential of urea and benzamide
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Crystal engineering and pharmaceutical crystallization
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Other Six-Membered Rings With Four or Five Nitrogen, Oxygen, or Sulfur
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Pharmaceutical solvates, hydrates and amorphous forms: A special emphasis on cocrystals
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Drug-drug cocrystals: Opportunities and challenges
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In - situ synchrotron wide-angle X-ray diffraction as a rapid method for cocrystal/salt screening
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Novel cocrystals of itraconazole: Insights from phase diagrams, formation thermodynamics and solubility
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Development of favipiravir dry powders for intranasal delivery: An integrated cocrystal and particle engineering approach via spray freeze drying
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Multicomponent hydrogen-bonding organic solids constructed from 6-hydroxy-2-naphthoic acid and N-heterocycles: Synthesis, structural characterization and synthon discussion
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Seven cocrystals of pyrazinamide and organic acids by H-bonds and some noncovalent associations
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A drug–drug cocrystal strategy to regulate stability and solubility: A case study of temozolomide/caffeic acid
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Temozolomide cocrystal forms with enhanced dissolution, stability and biological activity towards Glioblastoma
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Decoding intermolecular forces in drug Co-Crystallization: A Temozolomide-p-Coumaric acid system with enhanced stability and tunable dissolution profiles
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Temozolomide–Hesperetin Drug–Drug Cocrystal with Optimized Performance in Stability, Dissolution, and Tabletability
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Novel Drug–Drug Multicomponent Crystals of Epalrestat–Metformin: Improved Solubility and Photostability of Epalrestat and Reduced Hygroscopicity of Metformin
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Drug–Drug Multicomponent Crystals of Epalrestat: A Novel Form of the Drug Combination and Improved Solubility and Photostability of Epalrestat
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Five Cocrystal Forms of Antitumor Drug Temozolomide with p-Hydroxybenzoic Acid: Structure, Computational Analysis, Characterizations, Stability, and Transformation
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Structure Characterization and Property Evaluation of a Drug–Drug Cocrystal Involving Temozolomide and Luteolin
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Crystal Engineering: A Remedy To Tailor the Biopharmaceutical Aspects of Glibenclamide
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Crystal Engineering of Naturally Occurring Seselin To Obtain Cocrystal with Enhanced Anti-Leishmanial Activity, Hirshfeld Surface Analysis, and Computational Insight
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Constructing Anti-Glioma Drug Combination with Optimized Properties through Cocrystallization
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Tuning the Apparent Stability of Polymorphic Cocrystals through Mechanochemistry
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Crystal Engineering of Pharmaceutical Cocrystals in the Discovery and Development of Improved Drugs
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Importance of Thermal Stability Data to Avoid Dangerous Reagents: Temozolomide Case Study
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Temozolomide–Doxorubicin Conjugate as a Double Intercalating Agent and Delivery by Apoferritin for Glioblastoma Chemotherapy
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Cocrystals of fisetin, luteolin and genistein with pyridinecarboxamide coformers: crystal structures, analysis of intermolecular interactions, spectral and thermal characterization
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Polymorphism in cocrystals: a review and assessment of its significance
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Synthon polymorphs of 1 : 1 co-crystal of 5-fluorouracil and 4-hydroxybenzoic acid: their relative stability and solvent polarity dependence of grinding outcomes
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Mechanistic study of the hydrolytic degradation and protonation of temozolomide
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