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The role of co-crystals in pharmaceutical design
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Concepts and Nomenclature in Chemical Crystallography
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Principles and Applications of Thermal Analysis
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Polymorphism in the Pharmaceutical Industry
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Supramolecular Synthons in Crystal Engineering—A New Organic Synthesis
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Structure Calculation of an Elastic Hydrogel from Sonication of Rigid Small Molecule Components
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A Red Zwitterionic Co-Crystal of Acetaminophen and 2,4-Pyridinedicarboxylic Acid
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Polymorphie und Thermische Analyse pharmazeutischer Wirkstoffe
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On the polymorphism of pharmaceuticals and other molecular crystals. I
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On the polymorphism of pharmaceuticals and other molecular crystals. II
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�ber die Verwendung von Perjodat zur ma�analytischen Bestimmung von Ketosen (Monosacchariden)
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Use of a Glutaric Acid Cocrystal to Improve Oral Bioavailability of a Low Solubility API
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Cocrystal Formation during Cogrinding and Storage is Mediated by Amorphous Phase
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The role of cocrystals in pharmaceutical science
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Formation of indomethacin–saccharin cocrystals using supercritical fluid technology
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Computational prediction of salt and cocrystal structures—Does a proton position matter?
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Synthesis of co-crystals of meloxicam with carboxylic acids by grinding
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Cyclodextrins and their uses: a review
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Diversity in Single- and Multiple-Component Crystals. The Search for and Prevalence of Polymorphs and Cocrystals
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Cocrystal Systems of Pharmaceutical Interest: 2010
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Polymorphs, Salts, and Cocrystals: What’s in a Name?
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Applying Hot-Stage Microscopy to Co-Crystal Screening: A Study of Nicotinamide with Seven Active Pharmaceutical Ingredients
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Recent Advances in Understanding the Mechanism of Cocrystal Formation via Grinding
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Designing Co-Crystals of Pharmaceutically Relevant Compounds That Crystallize with Z′ > 1
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Solubility Advantage of Pharmaceutical Cocrystals
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A Survey of Cocrystals Reported Prior to 2000
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Hydrogen bond directed cocrystallization and molecular recognition properties of acyclic imides
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Hydrogen bond-directed cocrystallization and molecular recognition properties of diarylureas
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Physics and Chemistry of the Organic Solid State.
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Crystal Engineering Approach To Forming Cocrystals of Amine Hydrochlorides with Organic Acids. Molecular Complexes of Fluoxetine Hydrochloride with Benzoic, Succinic, and Fumaric Acids
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Using Cocrystals To Systematically Modulate Aqueous Solubility and Melting Behavior of an Anticancer Drug
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Cocrystal or Salt: Does It Really Matter?
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The Salt−Cocrystal Continuum: The Influence of Crystal Structure on Ionization State
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An Overview of Pharmaceutical Cocrystals as Intellectual Property
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Hierarchy of Supramolecular Synthons: Persistent Hydroxyl···Pyridine Hydrogen Bonds in Cocrystals That Contain a Cyano Acceptor
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Pharmaceutical Solids: A Strategic Approach to Regulatory Considerations
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Inclusion of the Antidepressant Paroxetine in β-cyclodextrin
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Modular and predictable assembly of porous organic molecular crystals
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Room-temperature ferroelectricity in supramolecular networks of charge-transfer complexes
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Hybrid insulin cocrystals for controlled release delivery
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A novel class of phenol–pyridine co-crystals for second harmonic generation
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Mechanochemistry and co-crystal formation: effect of solvent on reaction kineticsElectronic supplementary information (ESI) available for PXRD profiles showing the grinding results for CTA + Bipy with and without solvent as well as CTA + 2fPh with different solvents. See…
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Unexpected solid–solid reaction upon preparation of KBr pellets and its exploitation in supramolecular cation complexation
inferredcites →https://doi.org/10.1039/b315687gopenalex-snapshot
Crystal and co-crystal: a second opinion
inferredcites →https://doi.org/10.1039/b402150aopenalex-snapshot
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inferredcites →https://doi.org/10.1039/b505883jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/b516057jopenalex-snapshot
NMR studies of organic polymorphs & solvates
inferredcites →https://doi.org/10.1039/b803866jopenalex-snapshot
Current directions in co-crystal growth
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/c0cc02701dopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c0ce00052copenalex-snapshot
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inferredcites →https://doi.org/10.1039/c1cc10762copenalex-snapshot
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inferredcites →https://doi.org/10.1039/c1cs15171aopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c2ce06659aopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c2nj40093fopenalex-snapshot
How good are the crystallisation methods for co-crystals? A comparative study of piroxicam
inferredcites →https://doi.org/10.1080/713738904openalex-snapshot
Recent Advances in the Opportunities for Solving Molecular Crystal Structures Directly from Powder Diffraction Data
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Encyclopedia of Supramolecular Chemistry
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Polymorphism in Molecular Crystals
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2′,3′-Didehydro-3′-deoxythymidine N-methyl-2-pyrrolidone solvate (D4T·NMPO)
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Structures of two binary n-alkane solid solutions
inferredcites →https://doi.org/10.1107/s0108768197008446openalex-snapshot
Crystal Engineering: Strategies and Architectures
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Thermische Analyse im heizbaren Mikroskop
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Pharmaceutical Cocrystals: An Emerging Approach to Physical Property Enhancement
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X-ray and Neutron Diffraction in the Study of Organic Crystalline Hydrates
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Scalability of Pharmaceutical Co‐Crystal Formation by Mechanochemistry in Batch
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Changes in the proportions of an active pharmaceutical through cocrystals
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Unsymmetrical Bipyrrole‐Derived β‐Tetraalkylporphycenes and C–H···Br–C Interaction Induced 2D Arrays of the 2:1 Supramolecular Sandwich Complex of Their cis‐/trans‐Dibromo Isomers
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inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133256openalex-snapshot
Noncovalent-bonded 2D-3D supramolecular adducts from 6-methylpyridine-3-carboxamide and carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136942openalex-snapshot
Molecular structures of eight hydrogen bond-mediated minoxidil adducts from different aryl acids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137386openalex-snapshot
Solid state synthesis of zwitterionic cocrystal 5-fluorouracil L-phenylalanine explicated via structural, spectroscopy, quantum chemicals, Hirshfeld and docking analysis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140328openalex-snapshot
Regulating the physical and chemical properties of gefitinib and its positional isomer through salt formation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143028openalex-snapshot
Structural elucidation of unforeseen salt hydrate of gliclazide for enhanced solubility and dissolution rate
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143071openalex-snapshot
Pyrimethamine as a building block for 8 multicomponent crystals: Preparation, spectral, structural diversity, synthons investigation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145400openalex-snapshot
Structural and computational insights into ternary cocrystals of succinimide with 3-nitrophthalic acid and urea
inferred← citeshttps://doi.org/10.1016/j.pcrysgrow.2016.07.001openalex-snapshot
Spring and parachute: How cocrystals enhance solubility
inferred← citeshttps://doi.org/10.1016/j.poly.2022.115848openalex-snapshot
Structural elucidation and cytotoxicity profile of neocuproine-Cu(II) and Cu(I)-based chemotherapeutic agents: Effect of picric acid-derived cocrystals
inferred← citeshttps://doi.org/10.1016/j.proche.2014.10.079openalex-snapshot
Pharmaceutical Cocrystals
inferred← citeshttps://doi.org/10.1016/j.ssnmr.2014.11.002openalex-snapshot
NMR crystallography of ezetimibe co-crystals
inferred← citeshttps://doi.org/10.1016/j.tifs.2021.01.035openalex-snapshot
Cocrystallization: A tool to modulate physicochemical and biological properties of food-relevant polyphenols
inferred← citeshttps://doi.org/10.1016/j.tips.2018.10.006openalex-snapshot
Pharmaceutical Cocrystal Drug Products: An Outlook on Product Development
inferred← citeshttps://doi.org/10.1016/j.xphs.2016.08.029openalex-snapshot
The Crystal Structure and Behavior of Fenamic Acid-Acridine Complex Under High Pressure
inferred← citeshttps://doi.org/10.1016/j.xphs.2018.02.014openalex-snapshot
Improved Stability of Tuberculosis Drug Fixed-Dose Combination Using Isoniazid-Caffeic Acid and Vanillic Acid Cocrystal
inferred← citeshttps://doi.org/10.1016/j.xphs.2019.03.014openalex-snapshot
Polymorphs of Curcumin and Its Cocrystals With Cinnamic Acid
inferred← citeshttps://doi.org/10.1016/j.xphs.2020.03.017openalex-snapshot
Polymorphs of DP-VPA Solid Solutions and Their Physicochemical Properties
inferred← citeshttps://doi.org/10.1016/j.xphs.2021.08.009openalex-snapshot
Zaltoprofen/4,4′-Bipyridine: A Case Study to Demonstrate the Potential of Differential Scanning Calorimetry (DSC) in the Pharmaceutical Field
inferred← citeshttps://doi.org/10.1016/j.xphs.2022.08.031openalex-snapshot
Mechanistic Study on Transformation of Coamorphous Baicalein-Nicotinamide to Its Cocrystal Form
inferred← citeshttps://doi.org/10.1017/9781139026949.002openalex-snapshot
Crystals and Crystal Growth
inferred← citeshttps://doi.org/10.1021/acs.analchem.8b01112openalex-snapshot
Triboluminescence from Pharmaceutical Formulations
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00149openalex-snapshot
Discovery of New Proxyphylline-Based Chiral Cocrystals: Solid State Landscape and Dehydration Mechanism
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00266openalex-snapshot
Enhanced Aqueous Solubility of the Solid Forms of a BCS Class-II Anti-Tuberculosis Drug, Prothionamide
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00490openalex-snapshot
Cocrystal Polymorphs and Solvates of the Anti-Trypanosoma cruzi Drug Benznidazole with Improved Dissolution Performance
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00900openalex-snapshot
Natural Antimicrobials Meet a Synthetic Antibiotic: Carvacrol/Thymol and Ciprofloxacin Cocrystals as a Promising Solid-State Route to Activity Enhancement
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c01153openalex-snapshot
Temozolomide–Hesperetin Drug–Drug Cocrystal with Optimized Performance in Stability, Dissolution, and Tabletability
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c01427openalex-snapshot
Advanced Methodologies for Pharmaceutical Salt Synthesis
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c00216openalex-snapshot
Solvent Effect on the Preparation of Ionic Cocrystals of dl -Amino Acids with Lithium Chloride: Conglomerate versus Racemate Formation
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c00643openalex-snapshot
Self-Assemblies of Solvates, Ionic Cocrystals, and a Salt Based on 4-{[(4-Nitrophenyl)carbamoyl]amino}-N-(pyrimidin-2-yl)benzene-1-sulfonamide: Study in the Solid and Solution States
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c00768openalex-snapshot
Analysis of Weak Interactions in Crystals of Fenamic Acids–Ethacridine Complexes
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c01408openalex-snapshot
A Review on Co-crystals of Herbal Bioactives for Solubility Enhancement: Preparation Methods and Characterization Techniques
inferred← citeshttps://doi.org/10.1021/acs.cgd.1c01435openalex-snapshot
Inhibition of the Antibiotic Activity of Cephalosporines by Co-Crystallization with Thymol
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00262openalex-snapshot
On the Mechanism of Cocrystal Mechanochemical Reaction via Low Melting Eutectic: A Time-Resolved In Situ Monitoring Investigation
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00639openalex-snapshot
Preference of High-Nitrogen-Content Compounds to Form Hydrates and the Tandem Contacts of Azide Groups
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00896openalex-snapshot
Directional Self-Assembly of Ofloxacin and Syringic Acid: The First Salt Cocrystal of Ofloxacin with Phenolic Acid Displays Superior In Vitro/Vivo Biopharmaceutical Property and Enhanced Antibacterial Activity
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00904openalex-snapshot
Multivariate Analysis of a Highly Effective Drug Combination Tablet Containing the Antiepileptic Drug Gabapentin to Enhance Pharmaceutical Properties with a Multicomponent Crystal Strategy
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00996openalex-snapshot
Isomeric Coformer Responsive Conformational Adjustment to Recuperate Stability, Solubility, and In Vitro Permeation Behavior of Drug Molecular Salts
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c01142openalex-snapshot
Crystallographic and Computational Analysis of the Solid-Form Landscape of Three Structurally Related Imidazolidine-2,4-dione Active Pharmaceutical Ingredients: Nitrofurantoin, Furazidin, and Dantrolene
inferred← citeshttps://doi.org/10.1021/acs.cgd.2c01256openalex-snapshot
Syntheses, Structures, and Magnetic Properties of Novel [3×1 + 2×1] Pentanuclear Zinc(II)-Lanthanide(III) Cocrystal Complexes: Slow Magnetic Relaxation Behavior of the Dy(III) Analogue
inferred← citeshttps://doi.org/10.1021/acs.cgd.3c00042openalex-snapshot
Conjugation of a Silver-Based Coordination Polymer with Curcumin: A New Case of an Inorganic Polymeric Co-crystal
inferred← citeshttps://doi.org/10.1021/acs.cgd.3c00615openalex-snapshot
Exploring the Co-Crystallization Landscape of One-Dimensional Coordination Polymers Using a Molecular Electrostatic Potential-Driven Approach
inferred← citeshttps://doi.org/10.1021/acs.cgd.5b00700openalex-snapshot
In Situ Monitoring of Antisolvent Cocrystallization by Combining Near-Infrared and Raman Spectroscopies
inferred← citeshttps://doi.org/10.1021/acs.cgd.5b00840openalex-snapshot
Supramolecular Gel Control of Cisplatin Crystallization: Identification of a New Solvate Form Using a Cisplatin-Mimetic Gelator
inferred← citeshttps://doi.org/10.1021/acs.cgd.5b01320openalex-snapshot
New Multicomponent Sulfadimethoxine Crystal Forms: Sulfonamides as Participants in Supramolecular Interactions
inferred← citeshttps://doi.org/10.1021/acs.cgd.5b01619openalex-snapshot
Crystal Engineering of Pharmaceutical Co-crystals: “NMR Crystallography” of Niclosamide Co-crystals
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00245openalex-snapshot
Enhancing the Oral Bioavailability of an Antiviral Drug Acyclovir by Crystal Engineering of Novel Pharmaceutical Cocrystals
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00555openalex-snapshot
Special Issue: Multi-Component Pharmaceutical Solids
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00704openalex-snapshot
Deciphering the Structural Dynamics and Attributes of Cocrystals Engineered from 2-Amino, 5-Nitrobenzoic Acid with Neutral Coformers: A Synergistic Experimental and Computational Exploration
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00735openalex-snapshot
Piracetam and Oxiracetam Afford Molecular, Cocrystalline, and Ionic Cocrystalline Solid Solutions
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c00755openalex-snapshot
Cocrystal Engineering-Based Strategies for Enhancing the Permeability of Poorly Permeable APIs
inferred← citeshttps://doi.org/10.1021/acs.cgd.5c01287openalex-snapshot
Unraveling the Impact of Fluorine Positioning in Crystal Packing: Halogen-Bonded Cocrystals of 4-Styrylpyridines with Pentafluoroiodobenzene
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00010openalex-snapshot
Drug Molecule Diflunisal Forms Crystalline Inclusion Complexes with Multiple Types of Linear Polymers
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00032openalex-snapshot
Chloral Hydrate Polymorphs and Cocrystal Revisited: Solving Two Pharmaceutical Cold Cases
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00200openalex-snapshot
Solvates, Salts, and Cocrystals: A Proposal for a Feasible Classification System
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00321openalex-snapshot
Heterometallic Copper(II)–Tin(II/IV) Salts, Cocrystals, and Salt Cocrystals: Selectivity and Structural Diversity Depending on Ligand Substitution and the Metal Oxidation State
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00491openalex-snapshot
Caffeine Co-Crystal Mechanics Evaluated with a Combined Structural and Spectroscopic Approach
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00544openalex-snapshot
Expanding the Pyridine–Formic Acid Cocrystal Landscape under Extreme Conditions
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b00552openalex-snapshot
Improving the Membrane Permeability of 5-Fluorouracil via Cocrystallization
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b01164openalex-snapshot
Catalytic Effect of Solvent Vapors on the Spontaneous Formation of Caffeine–Malonic Acid Cocrystal
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b01399openalex-snapshot
Design of Cocrystals for Molecules with Limited Hydrogen Bonding Functionalities: Propyphenazone as a Model System
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b01426openalex-snapshot
Ionic Cocrystals of Racemic and Enantiopure Histidine: An Intriguing Case of Homochiral Preference
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b01578openalex-snapshot
Dissolution Behavior of the Crystalline Inclusion Complex Formed by the Drug Diflunisal and Poly(ε-caprolactone)
inferred← citeshttps://doi.org/10.1021/acs.cgd.6b01669openalex-snapshot
Are Oxygen and Sulfur Atoms Structurally Equivalent in Organic Crystals?
inferred← citeshttps://doi.org/10.1021/acs.cgd.7b00322openalex-snapshot
Epalrestat–Cytosine Cocrystal and Salt Structures: Attempt To Control E,Z → Z,Z Isomerization
inferred← citeshttps://doi.org/10.1021/acs.cgd.7b00606openalex-snapshot
Molecular Salts of the Antidepressant Venlafaxine: An Effective Route to Solubility Properties Modifications
inferred← citeshttps://doi.org/10.1021/acs.cgd.8b00684openalex-snapshot
Stable Cocrystals and Salts of the Antineoplastic Drug Apatinib with Improved Solubility in Aqueous Solution
inferred← citeshttps://doi.org/10.1021/acs.cgd.8b00933openalex-snapshot
Creating Cocrystals: A Review of Pharmaceutical Cocrystal Preparation Routes and Applications
inferred← citeshttps://doi.org/10.1021/acs.cgd.8b01049openalex-snapshot
Investigation into the Structures and Properties of Multicomponent Crystals Formed from a Series of 7-Chloroquinolines and Aromatic Acids
inferred← citeshttps://doi.org/10.1021/acs.cgd.8b01298openalex-snapshot
Cocrystals, Salts, and Supramolecular Gels of Nonsteroidal Anti-Inflammatory Drug Niflumic Acid
inferred← citeshttps://doi.org/10.1021/acs.cgd.9b00145openalex-snapshot
Colossal Positive and Negative Axial Thermal Expansion Induced by Scissor-like Motion of a Two-Dimensional Hydrogen Bonded Network in an Organic Salt
inferred← citeshttps://doi.org/10.1021/acs.cgd.9b00931openalex-snapshot
Engineering a Remedy to Improve Phase Stability of Famotidine under Physiological pH Environments
inferred← citeshttps://doi.org/10.1021/acs.cgd.9b01195openalex-snapshot
Novel Pharmaceutical Cocrystals and Salts of Bumetanide
inferred← citeshttps://doi.org/10.1021/acs.cgd.9b01253openalex-snapshot
Calorimetric Determination of Cocrystal Thermodynamic Stability: Sulfamethazine–Salicylic Acid Case Study
inferred← citeshttps://doi.org/10.1021/acs.cgd.9b01310openalex-snapshot
5-Fluorouracil Cocrystals with Lipophilic Hydroxy-2-Naphthoic Acids: Crystal Structures, Theoretical Computations, and Permeation Studies
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00987openalex-snapshot
Crystal Engineering of Pharmaceutical Cocrystals in the Discovery and Development of Improved Drugs
inferred← citeshttps://doi.org/10.1021/acs.jcim.6c01386openalex-snapshot
A Multimodal Semi-Supervised Learning Framework for Pharmaceutical Cocrystals Prediction
inferred← citeshttps://doi.org/10.1021/acs.jctc.2c00343openalex-snapshot
A Hybrid Machine Learning Approach for Structure Stability Prediction in Molecular Co-crystal Screenings
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b01234openalex-snapshot
Synthesis and Pharmacological Characterization of 2-(2,6-Dichlorophenyl)-1-((1S,3R)-5-(3-hydroxy-3-methylbutyl)-3-(hydroxymethyl)-1-methyl-3,4-dihydroisoquinolin-2(1H)-yl)ethan-1-one (LY3154207), a Potent, Subtype Selective, and Orally Available Positive Allosteric Modulator of the Human Dopamine…
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00220openalex-snapshot
Bringing a Molecular Plus One: Synergistic Binding Creates Guest-Mediated Three-Component Complexes
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.4c00393openalex-snapshot
Highly Soluble Dacarbazine Multicomponent Crystals Less Prone to Photodegradation
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.9b00377openalex-snapshot
Molecular Interpretation of the Compaction Performance and Mechanical Properties of Caffeine Cocrystals: A Polymorphic Study
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00314openalex-snapshot
Opportunities and Challenges in Mechanochemical Cocrystallization toward Scaled-Up Pharmaceutical Manufacturing
inferred← citeshttps://doi.org/10.1021/acs.oprd.5b00279openalex-snapshot
Recrystallizing Primidone through Supercritical Antisolvent Precipitation
inferred← citeshttps://doi.org/10.1021/acs.oprd.6c00052openalex-snapshot
Systematic Scale-Up of Mechanochemical Paracetamol–Oxalic Acid Cocrystal Synthesis across Multiple Milling Technologies
inferred← citeshttps://doi.org/10.1021/acsabm.2c00404openalex-snapshot
Comparison of Antimicrobial and Antibiofilm Activity of Proflavine Co-crystallized with Silver, Copper, Zinc, and Gallium Salts
inferred← citeshttps://doi.org/10.1021/acschemneuro.1c00312openalex-snapshot
Novel Co-crystal of Pentoxifylline and Protocatechuic Acid Relieves Allodynia in Rat Models of Peripheral Neuropathic Pain and CRPS by Alleviating Local Tissue Hypoxia
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c01257openalex-snapshot
Dispensing Essential Oil Components through Cocrystallization: Sustainable and Smart Materials for Food Preservation and Agricultural Applications
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b04576openalex-snapshot
Designing a Palette of Cocrystals Based on Essential Oil Constituents for Agricultural Applications
inferred← citeshttps://doi.org/10.1021/cg400638gopenalex-snapshot
Ketoconazole Salt and Co-crystals with Enhanced Aqueous Solubility
inferred← citeshttps://doi.org/10.1021/cg401061topenalex-snapshot
Diversity in Itraconazole Cocrystals with Aliphatic Dicarboxylic Acids of Varying Chain Length
inferred← citeshttps://doi.org/10.1021/cg401660hopenalex-snapshot
Insight into the Mechanism of Formation of Channel Hydrates via Templating
inferred← citeshttps://doi.org/10.1021/cg4018807openalex-snapshot
Structural Insights into Proton Conduction in Gallic Acid–Isoniazid Cocrystals
inferred← citeshttps://doi.org/10.1021/cg500345aopenalex-snapshot
A Twist in Cocrystals of Salts: Changes in Packing and Chloride Coordination Lead to Opposite Trends in the Biopharmaceutical Performance of Fluoroquinolone Hydrochloride Cocrystals
inferred← citeshttps://doi.org/10.1021/cg501009copenalex-snapshot
Cocrystallization of Nutraceuticals
inferred← citeshttps://doi.org/10.1021/cg5014329openalex-snapshot
Cyclic Interconversion among Molecular Salts via Neat Grinding and Related Photoluminescence Properties
inferred← citeshttps://doi.org/10.1021/cr500564zopenalex-snapshot
Packing Problems: High Z ′ Crystal Structures and Their Relationship to Cocrystals, Inclusion Compounds, and Polymorphism
inferred← citeshttps://doi.org/10.1021/ja403264copenalex-snapshot
Crystal Engineering: From Molecule to Crystal
inferred← citeshttps://doi.org/10.1021/jp503256kopenalex-snapshot
Mechanochemical Synthesis of Bumetanide–4-Aminobenzoic Acid Molecular Cocrystals: A Facile and Green Approach to Drug Optimization
inferred← citeshttps://doi.org/10.1021/jp5123008openalex-snapshot
NMR Study of BA/FBA Cocrystal Confined Within Mesoporous Silica Nanoparticles Employing Thermal Solid Phase Transformation
inferred← citeshttps://doi.org/10.1021/jz501699hopenalex-snapshot
Monitoring Cocrystal Formation via In Situ Solid-State NMR
inferred← citeshttps://doi.org/10.1021/mp5004652openalex-snapshot
Pharmaceutical Cocrystals of Diflunisal and Diclofenac with Theophylline
inferred← citeshttps://doi.org/10.1038/s41598-017-04980-3openalex-snapshot
High Pressure Spectroscopic Investigation on Proton Transfer in Squaric Acid and 4,4′-Bipyridine Co-crystal
inferred← citeshttps://doi.org/10.1038/s42003-022-03776-0openalex-snapshot
A co-crystal berberine-ibuprofen improves obesity by inhibiting the protein kinases TBK1 and IKKɛ
inferred← citeshttps://doi.org/10.1039/bk9781782621737-00719openalex-snapshot
Crystal Engineering: State of the Art and Open Challenges
inferred← citeshttps://doi.org/10.1039/c3ce42415dopenalex-snapshot
Crystal engineering of homochiral molecular organization of naproxen in cocrystals and their thermal phase transformation studies
inferred← citeshttps://doi.org/10.1039/c3ce42457jopenalex-snapshot
Continuous cocrystallisation of carbamazepine and trans-cinnamic acid via melt extrusion processing
inferred← citeshttps://doi.org/10.1039/c3cs60224aopenalex-snapshot
Supramolecular gel phase crystallization: orthogonal self-assembly under non-equilibrium conditions
inferred← citeshttps://doi.org/10.1039/c3sc51419fopenalex-snapshot
The curious case of (caffeine)·(benzoic acid): how heteronuclear seeding allowed the formation of an elusive cocrystal
inferred← citeshttps://doi.org/10.1039/c4cc00159aopenalex-snapshot
Co-crystal formation between poly(ethylene glycol) and a small molecular drug griseofulvin
inferred← citeshttps://doi.org/10.1039/c4ce00127copenalex-snapshot
Pharmaceutical co-crystals – are we there yet?
inferred← citeshttps://doi.org/10.1039/c4ce00316kopenalex-snapshot
Knowledge-based approaches to co-crystal design
inferred← citeshttps://doi.org/10.1039/c4ce00666fopenalex-snapshot
Structural and physicochemical aspects of hydrochlorothiazide co-crystals
inferred← citeshttps://doi.org/10.1039/c4ce01150copenalex-snapshot
2 : 1 5-Fluorocytosine–acesulfame CAB cocrystal and 1 : 1 5-fluorocytosine–acesulfame salt hydrate with enhanced stability against hydration
inferred← citeshttps://doi.org/10.1039/c4ce02044hopenalex-snapshot
Pharmaceutical cocrystals of the anti-tuberculosis drug pyrazinamide with dicarboxylic and tricarboxylic acids
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