17 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
53
Discovery of a potent enoyl-acyl carrier protein reductase (FabI) inhibitor suitable for antistaphylococcal agent.

The Catholic University of Korea
14
From triclosan toward the clinic: discovery of nonbiocidal, potent FabI inhibitors for the treatment of resistant bacteria.

Mutabilis
31
Discovery and Optimization of Novel SaFabI Inhibitors as Specific Therapeutic Agents for MRSA Infection.

Sichuan University
43
FabI (enoyl acyl carrier protein reductase) - A potential broad spectrum therapeutic target and its inhibitors.

National Institute of Pharmaceutical Education and Research (NIPER)
11
Spiro-naphthyridinone piperidines as inhibitors of S. aureus and E. coli enoyl-ACP reductase (FabI).

Affinium Pharmaceuticals
48
Aniline derivative, pharmaceutical composition containing same, and use thereof

Kissei Pharmaceutical
237
Heterocyclic derivative and pharmaceutical drug

Nippon Shinyaku
134
Compounds and methods for treating tuberculosis infection

Academia Sinica
2
Analysis of the Resistance Mechanism of a Benzoxaborole Inhibitor Reveals Insight into the Leucyl-tRNA Synthetase Editing Mechanism.

Ujf-Embl-Cnrs
190
SALT-INDUCIBLE KINASE INHIBITOR COMPOUND AND PHARMACEUTICAL COMPOSITION INCLUDING THE SAME

Mitsubishi Tanabe Pharma
20
Functional and radioligand binding characterization of rat 5-HT6 receptors stably expressed in HEK293 cells.

F. Hoffmann-La Roche
75
Binding characteristics of a radiolabeled agonist and antagonist at central nervous system alpha noradrenergic receptors.

TBA
207
Compound and composition as PDGF receptor kinase inhibitor

Nippon Shinyaku
70
2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1.

Glaxosmithkline
35
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studies.

Dupont Pharmaceuticals
9
Stereoisomers of cyclic urea HIV-1 protease inhibitors: synthesis and binding affinities.

Dupont Pharmaceuticals