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Crystal Engineering of Novel Cocrystals of a Triazole Drug with 1,4-Dicarboxylic Acids

https://doi.org/10.1021/ja035776p
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What points at this work

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inferred← citeshttps://doi.org/10.1016/j.ejps.2017.07.004openalex-snapshot
Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index
inferred← citeshttps://doi.org/10.1016/j.ejps.2019.104961openalex-snapshot
Crystalline adduct of moxifloxacin with trans-cinnamic acid to reduce the aqueous solubility and dissolution rate for improved residence time in the lungs
inferred← citeshttps://doi.org/10.1016/j.eng.2017.03.022openalex-snapshot
Recent Developments in the Crystallization Process: Toward the Pharmaceutical Industry
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e04864openalex-snapshot
Diclofenac-proline nano-co-crystal development, characterization, in vitro dissolution and diffusion study
inferred← citeshttps://doi.org/10.1016/j.ica.2010.08.044openalex-snapshot
Syntheses, crystal structures and magnetic properties of trinuclear and [3 × 1 + 1 × 2] pentanuclear complexes derived from a compartmental ligand: Role of solvent on nuclearity and number of components
inferred← citeshttps://doi.org/10.1016/j.ica.2013.01.006openalex-snapshot
Diversity in supramolecular self-assembly through hydrogen-bonding interactions of non-coordinated aliphatic –OH group in a series of heterodinuclear CuIIM (M = NaI, ZnII, HgII, SmIII, BiIII, PbII and CdII)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.124232openalex-snapshot
Discovery of novel benzenesulfonamides incorporating 1,2,3-triazole scaffold as carbonic anhydrase I, II, IX, and XII inhibitors
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2008.08.029openalex-snapshot
On the thermodynamics of cocrystal formation
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2009.03.016openalex-snapshot
Modeling and prediction of cocrystal phase diagrams
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2010.09.039openalex-snapshot
Inorganic-polymer nanohybrid carrier for delivery of a poorly-soluble drug, ursodeoxycholic acid
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2011.07.037openalex-snapshot
Pharmaceutical cocrystals: An overview
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.06.045openalex-snapshot
A new cocrystal and salts of itraconazole: Comparison of solid-state properties, stability and dissolution behavior
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.07.038openalex-snapshot
Establishment of cocrystal cocktail grinding method for rational screening of pharmaceutical cocrystals
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.09.045openalex-snapshot
Fast dissolving eutectic compositions of curcumin
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.10.043openalex-snapshot
Pharmaceutical cocrystals and poorly soluble drugs
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.11.020openalex-snapshot
High-throughput 96-well solvent mediated sonic blending synthesis and on-plate solid/solution stability characterization of pharmaceutical cocrystals
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2012.11.028openalex-snapshot
Use of pharmaceutical salts and cocrystals to address the issue of poor solubility
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2013.05.048openalex-snapshot
Pharmaceutical characterisation and evaluation of cocrystals: Importance of in vitro dissolution conditions and type of coformer
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2018.02.005openalex-snapshot
Surface area normalized dissolution to study differences in itraconazole-copovidone solid dispersions prepared by spray-drying and hot melt extrusion
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2019.118914openalex-snapshot
Microstructures and pharmaceutical properties of ferulic acid agglomerates prepared by different spherical crystallization methods
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2021.120441openalex-snapshot
Novel cocrystals of itraconazole: Insights from phase diagrams, formation thermodynamics and solubility
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2024.123944openalex-snapshot
Trace polymer coated clarithromycin spherulites: Formation mechanism, improvement in pharmaceutical properties and development of high-drug-loading direct compression tablets
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2025.126482openalex-snapshot
Combining crystal engineering and surface engineering to estimate the structure -functions relationship of Tafamidis solid state forms with the aid of machine learning
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2008.03.039openalex-snapshot
Growth and characterization of novel ferroelectric urea–succinic acid single crystals
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2011.09.020openalex-snapshot
Effects of some polymeric additives on the cocrystallization of caffeine
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2011.09.032openalex-snapshot
Pharmaceutical cocrystals: a comparison of sulfamerazine with sulfamethazine
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2023.127483openalex-snapshot
Synthesis, crystal growth, and its characterization of 2-amino-4-methylpyridinium oxalate
inferred← citeshttps://doi.org/10.1016/j.jddst.2017.04.001openalex-snapshot
Electrospray technology as a probe for cocrystal synthesis: Influence of solvent and coformer structure
inferred← citeshttps://doi.org/10.1016/j.jddst.2020.102236openalex-snapshot
Improvement of Physico-mechanical and pharmacokinetic attributes of naproxen by cocrystallization with l-alanine
inferred← citeshttps://doi.org/10.1016/j.jddst.2022.103757openalex-snapshot
An outlook on permeability escalation through cocrystallization for developing pharmaceuticals with improved biopharmaceutical properties
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.124395openalex-snapshot
Physicochemical properties and biological activities of new berberine-based salts with syringic acid as well as 3,5-dimethoxybenzoic acid as anions: Effect of temperature, concentration and anion
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.05.008openalex-snapshot
Preferential deprotonation and conformational stability of dicarboxylic acids: A packing effect
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.07.005openalex-snapshot
Solid state structural study on recognition of aromatic dicarboxylic acids by substituted amino-pyrimidines and its supramolecular network
inferred← citeshttps://doi.org/10.1016/j.molstruc.2007.08.025openalex-snapshot
Synthesis, crystal structure and theoretical investigation of two infinite two-dimensional supra-molecular compounds
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.01.021openalex-snapshot
Cocrystals of Kemp’s triacid. Part II. Molecular structure of the complex of Kemp’s triacid with 1,8-diazabicyclo[5.4.0]undec-7-ene
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.06.011openalex-snapshot
Cocrystals of Kemp’s triacid. Part III: Structure of hydrogen-bonded complex of Kemp’s triacid with 1,1,3,3-tetramethylguanidine studied by X-ray and FT-IR methods
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.01.045openalex-snapshot
Crystals of the Kemp’s triacid salts. Part IV: Supramolecular architecture in the crystal of tetra(melaminium) bis(5-carboxy-1,3,5-trimethylcyclo-hexane-1,3-dicarboxylate) pentahydrate
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.08.029openalex-snapshot
Hydrogen bond-directed co-crystals of (±)-1,1′-binaphthalene-2,2′-diol with aromatic diimines: Structures and selectivity
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.04.005openalex-snapshot
Crystals of the Kemp’s triacid salts – Part VI: Supramolecular architecture in the crystal of Kemp’s triacid with tris(2-aminoethyl)amine
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.08.005openalex-snapshot
Syntheses, crystal structures and supramolecular topologies of copper(II)–main group metal complexes derived from N,N′-o-phenylenebis(3-ethoxysalicylaldimine)
inferred← citeshttps://doi.org/10.1016/j.molstruc.2011.11.022openalex-snapshot
Noncovalent interactions between classical supramolecular synthons in solution: Hydrogen bonding in hindered 2-acylaminopyridine/2-pyridone associates
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.04.065openalex-snapshot
Structural studies of 1-phenyl-2,3-dimethyl-5-oxo-1,2-dihydro-1H-pyrazol-4-ammonium 2[(2-carboxyphenyl) disulfanyl]benzoate
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.12.022openalex-snapshot
Syntheses, structural characterization, and DPPH radical scavenging activity of cocrystals of caffeine with 1- and 2-naphthoxyacetic acids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.12.032openalex-snapshot
Positronium formation studies in crystalline molecular complexes: Triphenylphosphine oxide – Acetanilide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.03.017openalex-snapshot
Molecular and crystal structure of a new polymorph of malonic acid with Z′=3
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.05.048openalex-snapshot
Exploring contribution of intermolecular interactions in supramolecular layered assembly of naphthyridine co-crystals: Insights from Hirshfeld surface analysis of their crystalline states
inferred← citeshttps://doi.org/10.1016/j.molstruc.2014.11.026openalex-snapshot
Synthesis, structural characterization and Hirshfeld analysis studies of three novel co-crystals of trans-4-[(2-amino-3,5-dibrobenzyl) amino] cyclohexanol with hydroxyl benzoic acids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2016.10.034openalex-snapshot
Cocrystals of kaempferol, quercetin and myricetin with 4,4′-bipyridine: Crystal structures, analyses of intermolecular interactions and antibacterial properties
inferred← citeshttps://doi.org/10.1016/j.molstruc.2016.11.063openalex-snapshot
Make and break - Facile synthesis of cocrystals and comprehensive dissolution studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.03.086openalex-snapshot
Structural and physicochemical characterization of pyridine derivative salts of anti-inflammatory drugs
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.07.037openalex-snapshot
Co-crystal of 4,4′ -sulfonyldianiline and hexamethylenetetramine: Supramolecular interactions and thermal stability studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128806openalex-snapshot
Improving solubility and intrinsic dissolution rate of ofloxacin API through salt formation via mechanochemical synthesis with diphenic acid
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130006openalex-snapshot
Improvement of the anti-Candida activity of itraconazole in the zebrafish infection model by its coordination to silver(I)
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130682openalex-snapshot
New solid forms of the diuretic compound 4-Chloro Salicylic Acid-5-Sulfonamide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133225openalex-snapshot
α-(1,2,3-Triazolyl)-acetophenone: Synthesis and theoretical studies of crystal and 2,4-dinitrophenylhydrazine cocrystal structures
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140143openalex-snapshot
Supramolecular and computational analysis of Fluconazole −2−chloro−5−nitrobenzoic acid cocrystal
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140220openalex-snapshot
Insight into the phase equilibrium of mycophenolic acid cocrystals
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140507openalex-snapshot
Unveiling the anticancer potential: Exploring 4-fluoro benzoic acid and piperazine through spectroscopic, X-ray diffraction, DFT and molecular docking analysis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142363openalex-snapshot
New multicomponent crystals of nevirapine with improvement on solubility: preparation, characterization, calculation and analysis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142470openalex-snapshot
Exploring the multicomponent organic crystals via supramolecular synthons and their applications: A review
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145315openalex-snapshot
Exploring chemical reactivity and molecular interactions of hydrochlorothiazide-isonicotinamide cocrystal hydrate: A comparative spectroscopic and quantum chemical study using hydrochlorothiazide-4-aminobenzoic acid cocrystal
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