PMID

Data

Article Title

Organization

Synthesis and biological evaluation of novel sulfonyl-naphthalene-1,4-diols as FabH inhibitors.

Portland State University

Synthesis and biological evaluation of a C5-biphenyl thiolactomycin library.

University of Birmingham

Structure-activity relationships at the 5-position of thiolactomycin: an intact (5R)-isoprene unit is required for activity against the condensing enzymes from Mycobacterium tuberculosis and Escherichia coli.

National Institute of Allergy and Infectious Diseases

Biphenyl-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme.

The University of Birmingham