Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives-Reference-Cited by-同舟云学术

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives

Published:2017-01 Issue: Volume:125 Page:1289-1299
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Salar Uzma,Khan Khalid Mohammed,Taha Muhammad,Ismail Nor Hadiani,Ali Basharat,Qurat-ul-Ain ,Perveen Shahnaz,Ghufran Mehreen,Wadood Abdul

Funder

Higher Education Commission (HEC) Pakistan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference38 articles.

1. Synthesis and antibacterial activity evaluation of metronidazole–triazole conjugates

2. Drug residue formation from ronidazole, a 5-nitroimidazole. VIII. Identification of the 2-methylene position as a site of protein alkylation

3. Anti-methicillin resistant Staphylococcus aureus activity, synergism with oxacillin and molecular docking studies of metronidazole-triazole hybrids

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