38 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Progress in the development of fatty acid synthase inhibitors as anticancer targets.

University of South Alabama
Fatty Acid Synthase (FASN) Inhibitors as Potential Treatment for Cancer, Obesity, and Liver Related Disorders.

Therachem Research Medilab (India)
Repositioning proton pump inhibitors as anticancer drugs by targeting the thioesterase domain of human fatty acid synthase.

Indiana University School of Medicine
Imidazopyridine-Based Fatty Acid Synthase Inhibitors That Show Anti-HCV Activity and in Vivo Target Modulation.

3-V Biosciences
The lipogenesis pathway as a cancer target.

Wayne State University
Fatty Acid synthase inhibitors as possible treatment for cancer: patent highlight.

TBA
Fatty acid synthase inhibitory activity of acylphloroglucinols isolated from Dryopteris crassirhizoma.

Korea Research Institute of Bioscience and Biotechnology
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
Synthesis and evaluation of analogues of S-adenosyl-L-methionine, as inhibitors of the E. coli cyclopropane fatty acid synthase.

Pierre and Marie Curie University
Discovery of BI 99179, a potent and selective inhibitor of type I fatty acid synthase with central exposure.

Boehringer Ingelheim Pharma
Discovery of novel fatty acid synthase (FAS) inhibitors based on the structure of ketoaceyl synthase (KS) domain.

Sichuan University
Fatty acid synthase inhibitors of phenolic constituents isolated from Garcinia mangostana.

Chinese Academy of Sciences
Novel fatty acid synthase (FAS) inhibitors: design, synthesis, biological evaluation, and molecular docking studies.

Institute of Pharmacology and Toxicology
1-Oxo-3-substitute-isothiochroman-4-carboxylic acid compounds: synthesis and biological activities of FAS inhibition.

Institute of Pharmacology & Toxicology
Amphiphilic glycoconjugates as potential anti-cancer chemotherapeutics.

Emory University
3-Aryl-4-hydroxyquinolin-2(1H)-one derivatives as type I fatty acid synthase inhibitors.

Merck Research Laboratories
Therapeutic Activity of the Lansoprazole Metabolite 5-Hydroxy Lansoprazole Sulfide in Triple-Negative Breast Cancer by Inhibiting the Enoyl Reductase of Fatty Acid Synthase.

Indiana University School of Medicine
Galloyl esters of trans-stilbenes are inhibitors of FASN with anticancer activity on non-small cell lung cancer cells.

National University of Singapore
Discovery and optimization of novel piperazines as potent inhibitors of fatty acid synthase (FASN).

Forma Therapeutics
Synthesis, biological activities, and docking studies of d-pantolactone derivatives as novel FAS inhibitors.

Third Institute of Oceanography
CT2108A and B: New fatty acid synthase inhibitors as antifungal agents.

Panlabs
Flavanone glycosides from Miconia trailii.

University of Mississippi
Application of a flexible synthesis of (5R)-thiolactomycin to develop new inhibitors of type I fatty acid synthase.

Johns Hopkins University
Design and synthesis of a series of bioavailable fatty acid synthase (FASN) KR domain inhibitors for cancer therapy.

Janssen Research and Development
A strategy for dual inhibition of the proteasome and fatty acid synthase with belactosin C-orlistat hybrids.

Baylor University
(-)-UB006: A new fatty acid synthase inhibitor and cytotoxic agent without anorexic side effects.

Yachaytech University
Compounds having PDE9A inhibitory activity, and pharmaceutical uses thereof

Korea Research Institute of Chemical Technology
6-(5-hydroxy-1H-pyrazol-1-yl)nicotinamide inhibitors of PHD

Takeda Pharmaceutical
Phenylpyrazole derivatives as potent ROCK1 and ROCK2 inhibitors

Bristol-Myers Squibb
Nostotrebin 6, a bis(cyclopentenedione) with cholinesterase inhibitory activity isolated from Nostoc sp. str. Lukesová 27/97.

Brno University of Technology
Histone deacetylase inhibitor of benzamides and use thereof

Shanghai Institute of Pharmaceutical Industry
Direct Staudinger-Phosphonite Reaction Provides Methylphosphonamidates as Inhibitors of CE4 De-N-acetylases.

University of Toronto
Substituted aminotetrahydrothiopyrans and derivatives thereof as dipeptidyl peptidase-IV inhibitors for the treatment of diabetes

Merck Sharp & Dohme
Crystal Structure of Schistosoma mansoni Arginase, a Potential Drug Target for the Treatment of Schistosomiasis

University of Pennsylvania
Inhibitors of C-FMS kinase

Janssen Pharmaceutica
Inhibitors of tubulin assembly identified through screening a compound library.

The Ohio State University