49 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Discovery of Selective Small Molecule Inhibitors of Monoacylglycerol Acyltransferase 3.

Pfizer
Discovery and optimization of adamantane carboxylic acid derivatives as potent diacylglycerol acyltransferase 1 inhibitors for the potential treatment of obesity and diabetes.

Korea Research Institute of Chemical Technology
Discovery of a Novel Series of N-Phenylindoline-5-sulfonamide Derivatives as Potent, Selective, and Orally Bioavailable Acyl CoA:Monoacylglycerol Acyltransferase-2 Inhibitors.

Takeda Pharmaceutical
Development of novel benzomorpholine class of diacylglycerol acyltransferase I inhibitors.

Merck Research Laboratories
Discovery of novel quinoline carboxylic acid series as DGAT1 inhibitors.

Merck Research Laboratories
Discovery of 6-phenylpyrimido[4,5-b][1,4]oxazines as potent and selective acyl CoA:diacylglycerol acyltransferase 1 (DGAT1) inhibitors with in vivo efficacy in rodents.

Amgen
Defining the key pharmacophore elements of PF-04620110: discovery of a potent, orally-active, neutral DGAT-1 inhibitor.

Pfizer
Synthesis and biological evaluation of aminobenzimidazole derivatives with a phenylcyclohexyl acetic acid group as anti-obesity and anti-diabetic agents.

Korea Research Institute of Chemical Technology
Identification and design of a novel series of MGAT2 inhibitors.

Astrazeneca
Lead optimization of a pyridine-carboxamide series as DGAT-1 inhibitors.

Merck Research Laboratories
Design and optimization of pyrazinecarboxamide-based inhibitors of diacylglycerol acyltransferase 1 (DGAT1) leading to a clinical candidate dimethylpyrazinecarboxamide phenylcyclohexylacetic acid (AZD7687).

Astrazeneca
Identification and preliminary characterization of a potent, safe, and orally efficacious inhibitor of acyl-CoA:diacylglycerol acyltransferase 1.

Abbott Laboratories
Intestinally Targeted Diacylglycerol Acyltransferase 1 (DGAT1) Inhibitors Robustly Suppress Postprandial Triglycerides.

TBA
Discovery of PF-04620110, a Potent, Selective, and Orally Bioavailable Inhibitor of DGAT-1.

TBA
Design and synthesis of potent carboxylic acid DGAT1 inhibitors with high cell permeability.

Prosidion
Discovery of orally active carboxylic acid derivatives of 2-phenyl-5-trifluoromethyloxazole-4-carboxamide as potent diacylglycerol acyltransferase-1 inhibitors for the potential treatment of obesity and diabetes.

Hoffmann-La Roche
Design of Next-Generation DGAT2 Inhibitor PF-07202954 with Longer Predicted Half-Life.

Pfizer
Discovery of

TBA
Benzimidazolone Derivatives as DGAT2 Inhibitors for Treating Diseases.

Smith, Gambrell & Russell
Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis.

Pfizer
Novel Diacylglycerol Acetyltransferase 2 Inhibitors for Treating Liver Diseases.

Smith, Gambrell & Russell
Monoacylglycerol Acyltransferase 2 (MGAT2) Inhibitors for the Treatment of Metabolic Diseases and Nonalcoholic Steatohepatitis (NASH).

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

Terns Pharmaceuticals
Discovery and Pharmacology of a Novel Class of Diacylglycerol Acyltransferase 2 Inhibitors.

Merck
Discovery of Tetralones as Potent and Selective Inhibitors of Acyl-CoA:Diacylglycerol Acyltransferase 1.

Glaxosmithkline
Discovery of dimethyl pent-4-ynoic acid derivatives, as potent and orally bioavailable DGAT1 inhibitors that suppress body weight in diet-induced mouse obesity model.

Wuxi Apptec (Shanghai)
Causes and Significance of Increased Compound Potency in Cellular or Physiological Contexts.

Merck
Discovery of an Orally Bioavailable Benzimidazole Diacylglycerol Acyltransferase 1 (DGAT1) Inhibitor That Suppresses Body Weight Gain in Diet-Induced Obese Dogs and Postprandial Triglycerides in Humans.

Novartis Institutes For Biomedical Research
PREPARATION OF FUSED AZOLE DERIVATIVES AS NOVEL DIACYLGLYCERIDE 0-ACYLTRANSFERASE 2 INHIBITORS

Merck Sharp & Dohme
PREPARATION OF TETRAHYDROINDAZOLE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS

Merck Sharp & Dohme
NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS

Merck Sharp & Dohme
COMBINATIONS OF DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITORS AND ACETYL-COA CARBOXYLASE INHIBITOR

Pfizer
Diacylglyceride O-acyltransferase 2 inhibitors

Merck Sharp & Dohme
NOVEL BIARYL DERIVATIVE USEFUL AS DIACYLGLYCEROL ACYLTRANSFERASE 2 INHIBITOR, AND USE THEREOF

Lg Chem
Diacylglycerol acyl transferase 2 inhibitor

Pfizer
Indazole derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2

Merck Sharp & Dohme
Diacylglycerol acyl transferase 2 inhibitor

Pfizer
Diacylglycerol acyl transferase 2 inhibitors

Pfizer
Indole derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2

Merck Sharp & Dohme
Tetrahydroisoquinoline derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2

Merck Sharp & Dohme
Isoquinoline derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2

Merck Sharpe & Dohme
Diacylglycerol acyltransferase 2 inhibitors

Pfizer
Diacylglycerol acyltransferase 2 inhibitors

Pfizer
Diacylglycerol acyl transferase 2 inhibitors

Pfizer
Tetrahydroisoquinoline derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2

Merck Sharp & Dohme
Diacylglycerol acyltransferase 2 inhibitors

Pfizer
Discovery of a potent, selective, and orally efficacious pyrimidinooxazinyl bicyclooctaneacetic acid diacylglycerol acyltransferase-1 inhibitor.

Astrazeneca