20 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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Isozyme-specific enzyme inhibitors. 11. L-homocysteine-ATP S-C5' covalent adducts as inhibitors of rat methionine adenosyltransferases.

TBA
Isozyme-specific enzyme inhibitors. 10. Adenosine 5'-triphosphate derivatives as substrates or inhibitors of methionine adenosyltransferases of rat normal and hepatoma tissues.

TBA
Discovery of Potent and Oral Bioavailable MAT2A Inhibitors for the Treatment of MTAP-Deleted Tumors.

Hubei Bio-Pharmaceutical Industrial Technological Institute
Design and Structural Optimization of Methionine Adenosyltransferase 2A (MAT2A) Inhibitors with High In Vivo Potency and Oral Bioavailability.

Guizhou University
Discovery of novel methionine adenosyltransferase 2A (MAT2A) allosteric inhibitors by structure-based virtual screening.

Orion Pharma
Leveraging Structure-Based Drug Design to Identify Next-Generation MAT2A Inhibitors, Including Brain-Penetrant and Peripherally Efficacious Leads.

Agios Pharmaceuticals
Overview of Methionine Adenosyltransferase 2A (MAT2A) as an Anticancer Target: Structure, Function, and Inhibitors.

China Pharmaceutical University
Fragment-Based Design of a Potent MAT2a Inhibitor and

Astrazeneca
Discovery of AG-270, a First-in-Class Oral MAT2A Inhibitor for the Treatment of Tumors with Homozygous

Agios Pharmaceuticals
Methionine Adenosyltransferase Inhibitors for the Treatment of Cancer.

Usona Institute
Exploiting binding-site arginines in drug design: Recent examples.

Prelude Therapeutics
Isozyme-specific enzyme inhibitors. 12. C- and N-methylmethionines as substrates and inhibitors of methionine adenosyltransferases of normal and hepatoma rat tissues.

TBA
WRN INHIBITORS

Nimbus Wadjet
COMPOUND AS ADENOSINE A2a RECEPTOR ANTAGONIST AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

Chong Kun Dang Pharmaceutical
IMIDAZO[1,2-A]PYRIDINE DERIVATIVES AS IRAK4 INHIBITORS AND THEIR USE IN THE TREATMENT OF DISEASE

Biogen Ma
5-SUBSTITUTED INDOLE 3-AMIDE DERIVATIVES, PREPARATION METHOD AND USE THEREOF

Origiant Pharmaceutical
Benzimidazoles and indoles as taro inhibitors

Merck Sharp & Dohme
Heterocyclic derivatives as PI3K inhibitors

Incyte
Piperidines as covalent menin inhibitors

The Regents of The University of Michigan
Compositions useful for treating disorders related to kit

Blueprint Medicines