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Synthesis and Antimicrobial Activity of 1,2-Benzothiazine Derivatives
Chandani Patel
, Jatinder Bassin
, Mark Scott
, Jenna Flye
, Ann Hunter
, Lee Martin
,
Madhu Goyal
Veterinary Science
Biosciences Research Group
Centre for Health Services and Clinical Research
Psychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
Centre for Research in Mechanisms of Disease and Drug Discovery
Department of Clinical, Pharmaceutical and Biological Science
Research output
:
Contribution to journal
›
Article
›
peer-review
45
Citations (Scopus)
169
Downloads (Pure)
Overview
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Keyphrases
Gram-positive Bacteria
100%
Antimicrobial Activity
100%
1,2-benzothiazine Derivatives
100%
Gram-negative Bacteria
66%
1,2-benzothiazine
66%
Salmonella Enterica Serovar Typhimurium (S. Typhimurium)
66%
Chalcone
66%
Bacillus Subtilis (B. subtilis)
66%
Bromine Atom
66%
Chlorine Atom
66%
Staphylococcus Aureus
66%
Structure-activity Relationship Studies
33%
Microdilution
33%
Glacial Acetic Acid
33%
Thiazine
33%
Aniline
33%
Step Processes
33%
Benzene Ring
33%
Fluoro
33%
Dilution Technique
33%
Bromine
33%
Para-position
33%
Ammonia
33%
Methylamine
33%
Chlorosulfonic Acid
33%
P. Vulgaris
33%
Proteus Vulgaris
33%
Broth
33%
Methyl
33%
Benzoyl
33%
Meta-position
33%
Hydrogen Atom
33%
Methyl Groups
33%
Ethyl
33%
Ethylamine
33%
Antibacterial Activity
33%
Bromo
33%
Chloro
33%
Sulfonyl Chlorides
33%
Benzylamine
33%
Pharmacology, Toxicology and Pharmaceutical Science
Gram Positive Bacterium
100%
Benzothiazine Derivative
100%
Antimicrobial Agent
100%
Gram Negative Bacterium
66%
Bacillus subtilis
66%
Benzothiazine
66%
Antibacterial Activity
33%
Structure Activity Relationship
33%
Ethylamine
33%
Benzylamine
33%
Chalcone Derivative
33%
Staphylococcus Aureus
33%
Methyl Group
33%
Chalcone
33%
Hydrogen
33%
Salmonella Enterica Serovar Typhimurium
33%
Sulfonyl
33%
Thiazine
33%
Potassium Acetate
33%
Methylamine
33%
Proteus vulgaris
33%