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Salts and Cocrystals of the Antidiabetic Drugs Gliclazide, Tolbutamide, and Glipizide: Solubility Enhancements through Drug–Coformer Interactions
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Conformational Polymorphism of Tolbutamide: A Structural, Spectroscopic, and Thermodynamic Characterization of Burger’s Forms I–IV
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A survey of Top 200 Drugs—Inconsistent Practice of Drug Strength Expression for Drugs Containing Salt Forms
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Thermodynamic Studies of Tolbutamide Polymorphs
inferredcites →https://doi.org/10.1007/s00125-012-2562-9openalex-snapshot
Cell signalling in insulin secretion: the molecular targets of ATP, cAMP and sulfonylurea
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Use of a Glutaric Acid Cocrystal to Improve Oral Bioavailability of a Low Solubility API
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Hydrogen-bonding directed cocrystallization of flexible piperazine with hydroxybenzoic acid derivatives: Structural diversity and synthon prediction
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Divergent cardiac effects of the first and second generation hypoglycemic sulfonylurea compounds
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The role of cocrystals in pharmaceutical science
inferredcites →https://doi.org/10.1016/j.metabol.2006.01.019openalex-snapshot
Gliclazide protects 3T3L1 adipocytes against insulin resistance induced by hydrogen peroxide with restoration of GLUT4 translocation
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Polymorphism of Mechanochemically Synthesized Cocrystals: A Case Study
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Solvates, Salts, and Cocrystals: A Proposal for a Feasible Classification System
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Drug–Drug Multicomponent Crystals as an Effective Technique to Overcome Weaknesses in Parent Drugs
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Cocrystal and Salt Forms of Furosemide: Solubility and Diffusion Variations
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Isostructural Multicomponent Gliclazide Crystals with Improved Solubility
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New Cocrystals of Hydrochlorothiazide: Optimizing Solubility and Membrane Diffusivity
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A Drug–Drug Salt Hydrate of Norfloxacin and Sulfathiazole: Enhancement of in Vitro Biological Properties via Improved Physicochemical Properties
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Solubility Advantage of Amorphous Drugs and Pharmaceutical Cocrystals
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Fast Dissolving Curcumin Cocrystals
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High Solubility Piperazine Salts of the Nonsteroidal Anti-Inflammatory Drug (NSAID) Meclofenamic Acid
inferredcites →https://doi.org/10.1021/cg3002948openalex-snapshot
Polymorphs, Salts, and Cocrystals: What’s in a Name?
inferredcites →https://doi.org/10.1021/cg4000457openalex-snapshot
Solubility Advantage of Tenoxicam Phenolic Cocrystals Compared to Salts
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New Solid Forms of the Anti-HIV Drug Etravirine: Salts, Cocrystals, and Solubility
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Solubility Advantage of Pharmaceutical Cocrystals
inferredcites →https://doi.org/10.1021/cg801122mopenalex-snapshot
Molecular Crystal Prediction Approach by Molecular Similarity: Data Mining on Molecular Aggregation Predictors and Crystal Descriptors
inferredcites →https://doi.org/10.1021/cg900129fopenalex-snapshot
Pharmaceutical Cocrystals and Their Physicochemical Properties
inferredcites →https://doi.org/10.1021/cg900873topenalex-snapshot
A Survey of Cocrystals Reported Prior to 2000
inferredcites →https://doi.org/10.1021/cg901002yopenalex-snapshot
The Reemergence of Cocrystals: The Crystal Clear Writing Is on the WallIntroduction to Virtual Special Issue on Pharmaceutical Cocrystals
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Solid-state reactivity of picric acid and substituted hydrocarbons
inferredcites →https://doi.org/10.1021/j100882a047openalex-snapshot
Solid-State Reactions between Picric Acid and Naphthols
inferredcites →https://doi.org/10.1021/ja907674copenalex-snapshot
Using Cocrystals To Systematically Modulate Aqueous Solubility and Melting Behavior of an Anticancer Drug
inferredcites →https://doi.org/10.1021/mp400516bopenalex-snapshot
Salt and Cocrystals of Sildenafil with Dicarboxylic Acids: Solubility and Pharmacokinetic Advantage of the Glutarate Salt
inferredcites →https://doi.org/10.1021/op900169bopenalex-snapshot
Why Do Organic Compounds Crystallise Well or Badly or Ever so Slowly? Why Is Crystallisation Nevertheless Such a Good Purification Technique?
inferredcites →https://doi.org/10.1039/b813401dopenalex-snapshot
Ziprasidone malate, a new trimorphic salt with improved aqueous solubility
inferredcites →https://doi.org/10.1039/c0ce00073fopenalex-snapshot
Novel form V of tolbutamide and a high Z′ crystal structure of form III
inferredcites →https://doi.org/10.1039/c2ce26325dopenalex-snapshot
Pharmaceutical cocrystals of ethenzamide: structural, solubility and dissolution studies
inferredcites →https://doi.org/10.1039/c3ce42013bopenalex-snapshot
A sildenafil cocrystal based on acetylsalicylic acid exhibits an enhanced intrinsic dissolution rate
inferredcites →https://doi.org/10.1039/c5cc08216aopenalex-snapshot
Pharmaceutical cocrystals: along the path to improved medicines
inferredcites →https://doi.org/10.1039/c5ce02402aopenalex-snapshot
Novel cocrystals of gliclazide: characterization and evaluation
inferredcites →https://doi.org/10.1107/s0021889802022112openalex-snapshot
Single-crystal structure validation with the program PLATON
inferredcites →https://doi.org/10.1107/s0021889897003117openalex-snapshot
ORTEP-3 for Windows - a version ofORTEP-III with a Graphical User Interface (GUI)
inferredcites →https://doi.org/10.1107/s0021889899006020openalex-snapshot
WinGX suite for small-molecule single-crystal crystallography
inferredcites →https://doi.org/10.1107/s0108768105025991openalex-snapshot
Structure and intermolecular interactions of glipizide from laboratory X-ray powder diffraction
inferredcites →https://doi.org/10.1177/104063870701900602openalex-snapshot
Assessment of Melamine and Cyanuric Acid Toxicity in Cats
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Physicochemical Properties of Nitrofurantoin Anhydrate and Monohydrate and Their Dissolution.
inferredcites →https://doi.org/10.1351/pac-rec-10-01-02openalex-snapshot
Definition of the hydrogen bond (IUPAC Recommendations 2011)
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Additional file 1 of Cocrystallization of gliclazide with improved physicochemical properties
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