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Synthesis, Characterization, Thermal and Antimicrobial studies of N-substituted Sulfanilamide derivatives

https://doi.org/10.1016/j.molstruc.2013.12.063

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What this work says

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

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Thermodynamic and structural aspects of sulfonamide crystals and solutions

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Polymorphism in Sulfonamides

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Crystal and molecular structure of 4-aminoacetyl-N-p-nitrophenylsulfanilamide

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Eimeria tenella: Anticoccidial drug activity in cell cultures

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Metal ions in biological systems

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The thermogravimetry of sulfanilamide and related sulfa drugs

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Hydroxytriamides as potent γ-secretase inhibitors

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Carbonic anhydrase inhibitors. Design of anticonvulsant sulfonamides incorporating indane moieties

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Synthesis and anticonvulsant activity of sulfonamide derivatives-hydrophobic domain

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Synthesis, characterization, antimicrobial and single crystal X-ray crystallographic studies of some new sulfonyl, 4-chloro phenoxy benzene and dibenzoazepine substituted benzamides

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Antimicrobial activity of sulfonamides containing 5-chloro-2-hydroxybenzaldehyde and 5-chloro-2-hydroxybenzoic acid scaffold

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Synthesis and antimalarial activity of sulfonamide chalcone derivatives

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Studying thermodynamic aspects of sublimation, solubility and solvation processes and crystal structure analysis of some sulfonamides

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Sulfonamides as a subject to study molecular interactions in crystals and solutions: Sublimation, solubility, solvation, distribution and crystal structure

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Copper complexes with heterocyclic sulfonamides: Synthesis, spectroscopic characterization, microbiological and SOD-like activities: Crystal structure of [Cu(sulfisoxazole)2(H2O)4]·2H2O

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A novel kind of antitumour drugs using sulfonamide as parent compound

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Sulfonamide Molecular Crystals: Thermodynamic and Structural Aspects

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Sulfonamide Molecular Crystals: Structure, Sublimation Thermodynamic Characteristics, Molecular Packing, Hydrogen Bonds Networks

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Stucture and Chemotherapeutic Activities of Sulfanilamide Derivatives.

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A Diverse Series of Substituted Benzenesulfonamides as Aldose Reductase Inhibitors with Antioxidant Activity: Design, Synthesis, and in Vitro Activity

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The influence of chemical structure of sulfonamides on the course of their thermal decomposition

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A facile, environmentally benign sulfonamide synthesis in water

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Isosterism and molecular modification in drug design

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Mercury CSD 2.0 – new features for the visualization and investigation of crystal structures

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Multiparametric scaling of diffraction intensities

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A short history of SHELX

inferredcites →https://doi.org/10.1107/s0108768101016858openalex-snapshot

Iodo-nitroarenesulfonamides: interplay of hard and soft hydrogen bonds, I...O interactions and aromatic π...π stacking interactions

inferredcites →https://doi.org/10.1107/s0108768102003890openalex-snapshot

The Cambridge Structural Database: a quarter of a million crystal structures and rising

inferredcites →https://doi.org/10.1107/s0108768107065895openalex-snapshot

Using small molecule crystal structure data to obtain information about sulfonamide conformation

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Drug Discovery: A Historical Perspective

inferredcites →https://doi.org/10.1146/annurev.pa.16.040176.001521openalex-snapshot

Relations Between Structure and Biological Activity of Sulfonamides

inferredcites →https://doi.org/10.1515/zna-2002-1210openalex-snapshot

Infrared and NMR Spectra of Arylsulphonamides, 4-X-C6H4SO2NH2 and i-X, j-YC6H3SO2NH2 (X=H; CH3; C2H5; F; Cl; Br; I or NO2 and i-X, j-Y=2,3-(CH3)2; 2,4-(CH3)2; 2,5- (CH3)2; 2-CH3, 4-Cl; 2-CH3, 5-Cl; 3-CH3, 4-Cl; 2,4-Cl2 or 3,4-Cl2)

inferredcites →https://doi.org/10.1517/13543776.10.5.575openalex-snapshot

Carbonic anhydrase inhibitors and their therapeutic potential

inferredcites →https://doi.org/10.2174/1389557043487402openalex-snapshot

Antiviral Sulfonamide Derivatives

inferredcites →https://doi.org/10.2174/1568013013359131openalex-snapshot

Carbonic Anhydrase Inhibitors

inferredcites →https://doi.org/10.5860/choice.40-3409openalex-snapshot

Chlorosulfonic acid: a versatile reagent

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

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