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

Pfizer
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
Identification and design of a novel series of MGAT2 inhibitors.

Astrazeneca
Design of Next-Generation DGAT2 Inhibitor PF-07202954 with Longer Predicted Half-Life.

Pfizer
Discovery of

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

Pfizer
Screening Hit to Clinical Candidate: Discovery of BMS-963272, a Potent, Selective MGAT2 Inhibitor for the Treatment of Metabolic Disorders.

TBA
Monoacylglycerol Acyltransferase 2 (MGAT2) Inhibitors for the Treatment of Metabolic Diseases and Nonalcoholic Steatohepatitis (NASH).

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

Merck
PHTHALAZINE DERIVATIVES AS PYRUVATE KINASE MODULATORS

Sitryx Therapeutics
ARYL HETEROCYCLIC COMPOUNDS AS Kv1.3 POTASSIUM SHAKER CHANNEL BLOCKERS

D.E. Shaw Research
Substituted amino acids as integrin inhibitors

Pliant Therapeutics
Substituted imidazopyridazines

Bayer Pharma Aktiengesellschaft
Substituted benzoxazoles

Bayer Pharma Aktiengesellschaft
Structural basis of pharmacological chaperoning for human ß-galactosidase.

The University of Tokyo
Synthesis and pharmacological characterization of novel xanthine carboxylate amides as A2A adenosine receptor ligands exhibiting bronchospasmolytic activity.

Panjab University
Cyclic ether DGAT1 inhibitorscyclic ether DGAT1 inhibitors

Novartis
Phenoxyethoxy compounds

Eli Lilly
Prokineticin receptor antagonists and uses thereof

University of California
Type II Ligands as Chemical Auxiliaries To Favor Enzymatic Transformations by P450 2E1.

Mcgill University