52 articles for thisTarget
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Discovery of N-(1-(3-(4-phenoxyphenyl)-1,2,4-oxadiazol-5-yl)ethyl)acetamides as novel acetyl-CoA carboxylase 2 (ACC2) inhibitors with peroxisome proliferator-activated receptora/d (PPARa/d) dual agonistic activity.

The University of Tokyo
Discovery of spirocyclic-diamine inhibitors of mammalian acetyl CoA-carboxylase.

Pfizer
Recent advances in the development of acetyl-CoA carboxylase (ACC) inhibitors for the treatment of metabolic disease.

Amgen
Decreasing the rate of metabolic ketone reduction in the discovery of a clinical acetyl-CoA carboxylase inhibitor for the treatment of diabetes.

Pfizer
Piperazine oxadiazole inhibitors of acetyl-CoA carboxylase.

Amgen
Spirolactam-based acetyl-CoA carboxylase inhibitors: toward improved metabolic stability of a chromanone lead structure.

Pfizer
Treatment of Obesity and Related Disorders with Acetyl-CoA Carboxylase Inhibitors.

Therachem Research Medilab (India)
The lipogenesis pathway as a cancer target.

Wayne State University
Symmetrical approach of spiro-pyrazolidinediones as acetyl-CoA carboxylase inhibitors.

Takeda Pharmaceutical
Design, synthesis, and structure-activity relationships of novel spiro-piperidines as acetyl-CoA carboxylase inhibitors.

Takeda Pharmaceutical
Discovery of novel (4-piperidinyl)-piperazines as potent and orally active acetyl-CoA carboxylase 1/2 non-selective inhibitors: F-Boc and triF-Boc groups are acid-stable bioisosteres for the Boc group.

Taisho Pharmaceutical
Synthesis and structure-activity relationships of N-{3-[2-(4-alkoxyphenoxy)thiazol-5-yl]-1- methylprop-2-ynyl}carboxy derivatives as selective acetyl-CoA carboxylase 2 inhibitors.

Abbott Laboratories
Maximizing lipophilic efficiency: the use of Free-Wilson analysis in the design of inhibitors of acetyl-CoA carboxylase.

Pfizer
Design, synthesis, and structure-activity relationships of spirolactones bearing 2-ureidobenzothiophene as acetyl-CoA carboxylases inhibitors.

Takeda Pharmaceutical
Design of small molecule inhibitors of acetyl-CoA carboxylase 1 and 2 showing reduction of hepatic malonyl-CoA levels in vivo in obese Zucker rats.

Astrazeneca Research and Development
Identification and synthesis of novel inhibitors of acetyl-CoA carboxylase with in vitro and in vivo efficacy on fat oxidation.

Sanofi-Aventis Deutschland
Discovery of small molecule isozyme non-specific inhibitors of mammalian acetyl-CoA carboxylase 1 and 2.

Pfizer
(4-Piperidinyl)-piperazine: a new platform for acetyl-CoA carboxylase inhibitors.

Taisho Pharmaceutical
Potent biphenyl- and 3-phenyl pyridine-based inhibitors of acetyl-CoA carboxylase.

Bristol-Myers Squibb Research and Development
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.

Johann Wolfgang Goethe University
2-hydroxy-N-arylbenzenesulfonamides as ATP-citrate lyase inhibitors.

Bristol-Myers Squibb Pharmaceutical Research Institute
N-{3-[2-(4-alkoxyphenoxy)thiazol-5-yl]-1-methylprop-2-ynyl}carboxy derivatives as acetyl-coA carboxylase inhibitors--improvement of cardiovascular and neurological liabilities via structural modifications.

Abbott Laboratories
Phenoxy thiazole derivatives as potent and selective acetyl-CoA carboxylase 2 inhibitors: Modulation of isozyme selectivity by incorporation of phenyl ring substituents.

Abbott Laboratories
The synthesis and structure-activity relationship studies of selective acetyl-CoA carboxylase inhibitors containing 4-(thiazol-5-yl)but-3-yn-2-amino motif: polar region modifications.

Abbott Laboratories
Structure-activity relationships for a novel series of thiazolyl phenyl ether derivatives exhibiting potent and selective acetyl-CoA carboxylase 2 inhibitory activity.

Abbott Laboratories
Design and synthesis of a monocyclic derivative as a selective ACC1 inhibitor by chemical modification of biphenyl ACC1/2 dual inhibitors.

Takeda Pharmaceutical
Optimizing the Benefit/Risk of Acetyl-CoA Carboxylase Inhibitors through Liver Targeting.

Pfizer
The identification and pharmacological evaluation of potent, selective and orally available ACC1 inhibitor.

Takeda Pharmaceutical
The Race to Bash NASH: Emerging Targets and Drug Development in a Complex Liver Disease.

Terns Pharmaceuticals
Design and synthesis of a novel 1H-pyrrolo[3,2-b]pyridine-3-carboxamide derivative as an orally available ACC1 inhibitor.

Takeda Pharmaceutical
Synthesis and characterization of a BODIPY-labeled derivative of Soraphen A that binds to acetyl-CoA carboxylase.

Novartis Institutes For Biomedical Research
Design, synthesis and biological evaluation of novel spiro-pentacylamides as acetyl-CoA carboxylase inhibitors.

China Pharmaceutical University
Discovery of a novel olefin derivative as a highly potent and selective acetyl-CoA carboxylase 2 inhibitor with in vivo efficacy.

Shionogi
Discovery of Novel Selective Acetyl-CoA Carboxylase (ACC) 1 Inhibitors.

Takeda Pharmaceutical
PLPRO PROTEIN INHIBITOR, AND PREPARATION METHOD AND APPLICATION THEREOF

Tsinghua University
Triazolopyrimidine compound and salt, composition and use thereof

Shanghai Institute Of Materia Medica
HETEROBIFUNCTIONAL MOLECULES AS TEAD INHIBITORS

Merck Patent
NUCLEAR TRANSPORT MODULATORS AND USES THEREOF

Karyopharm Therapeutics
Benzimidazole compounds and derivatives as EGFR inhibitors

Boehringer Ingelheim International
Combination of pure 5-HT6 receptor antagonists with NMDA receptor antagonist

Suven Life Sciences
Potent and selective mu opioid receptor modulators

Virginia Commonwealth University
Imidazolonylquinolines and the use thereof as ATM kinase inhibitors

Merck Patent
Synthesis and antiproliferative activities against Hep-G2 of salicylanide derivatives: potent inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase.

Nanjing University
Talaromyces marneffei Mp1p Is a Virulence Factor that Binds and Sequesters a Key Proinflammatory Lipid to Dampen Host Innate Immune Response.

The University of Hong Kong
mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction

Vanderbilt University
Azinone-substituted azepino[b]indole and pyrido-pyrrolo-azepine MCH-1 antagonists, methods of making, and use thereof

Albany Molecular Research
The rabbit motilin receptor: molecular characterisation and pharmacology.

Glaxosmithkline
Different binding affinities of NMDA receptor channel blockers in various brain regions--indication of NMDA receptor heterogeneity.

Merz
Human serotonin 1D receptor is encoded by a subfamily of two distinct genes: 5-HT1D alpha and 5-HT1D beta.

Synaptic Pharmaceutical
Structure-guided development of efficacious antifungal agents targeting Candida glabrata dihydrofolate reductase.

University of Connecticut