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Description Table
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description Some of the imidazopyridine based antitubercular agent.
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description A) Hydrophobic & B)Hydrophilic amino acids surrounded to compounds PINRAc‐11 & PINRAc‐8.
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description Synthetic route for the target compounds PINRAc(1–12).
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description Table
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description MmpL inhibitors exhibit structural diversity.
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description A) PINRAc‐11 in the proposed binding pocket of enzyme PDB ID: 6AJG B) Docked mode of the compound PINRAc‐11 C) 3D D) 2D representation of docked view of the compound PINRAc‐11 at the active site of...
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description A) PINRAc‐8 in the proposed binding pocket of enzyme PDB ID: 6AJG B) Docked mode of the compound PINRAc‐8 C) 3D D) 2D representation of docked view of the compound PINRAc‐11 at the active site of...
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description A) PINRAc (1–12) in the proposed binding pocket of enzyme PDB ID: 6AJG
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description A) Standard compound in the proposed binding pocket of enzyme PDB ID: 6AJG B) Docked view of the standard at the active site of enzyme PDB ID: 6AJG.
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents - ChemistrySelectChemistrySelect vol. 5, December 7, 2020
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect -
Description Drugs containing the imidazo[1,2‐a]pyridine core.
Article Title: Synthesis of 2‐Chloro‐N‐(4‐(6‐chloroH‐imidazo[1,2‐a]pyridin‐2‐yl)phenyl) Acetamide Derivatives as Antitubercular Agents
Publication Title: ChemistrySelect