Binding Database

19 articles for thisTarget

The following articles (labelled with PubMed ID or TBD) are for your review

PMID

Data

Article Title

Organization

Discovery of Dual Inhibitors for Wild Type and D816V Mutant of c-KIT Kinase through Virtual and Biochemical Screening of Natural Products.

Sejong University

26259807

Structure-based de novo design and synthesis of aminothiazole-based p38 MAP kinase inhibitors.

Sejong University

24393580

Virtual screening and biochemical evaluation to identify new inhibitors of mammalian target of rapamycin (mTOR).

Sejong University

22989533

Discovery of potent inhibitors of receptor protein tyrosine phosphatase sigma through the structure-based virtual screening.

Sejong University

22771009

Discovery of MEK/PI3K dual inhibitor via structure-based virtual screening.

Sejong University

19269068

Structure-based virtual screening approach to identify novel classes of PTP1B inhibitors.

Sejong University

15582436

N-hydroxy-2-(naphthalene-2-ylsulfanyl)-acetamide, a novel hydroxamic acid-based inhibitor of aminopeptidase N and its anti-angiogenic activity.

Sejong University

22342625

Structure-based virtual screening approach to the discovery of p38 MAP kinase inhibitors.

Sejong University

22196123

Structure-based de novo design and biochemical evaluation of novel BRAF kinase inhibitors.

Sejong University

21873050

Identification of novel BRAF kinase inhibitors with structure-based virtual screening.

Sejong University

21354792

Structure-based virtual screening approach to the discovery of phosphoinositide 3-kinase alpha inhibitors.

Sejong University

19822432

Structure-based virtual screening approach to the discovery of novel inhibitors of factor-inhibiting HIF-1: identification of new chelating groups for the active-site ferrous ion.

Sejong University

19500977

Structure-based virtual screening approach to identify novel classes of Cdc25B phosphatase inhibitors.

Sejong University

19497739

Structure-based de novo design and biochemical evaluation of novel Cdc25 phosphatase inhibitors.

Sejong University

18835158

Identification of novel inhibitors of extracellular signal-regulated kinase 2 based on the structure-based virtual screening.

Sejong University

18714978

Discovery of novel Cdc25 phosphatase inhibitors with micromolar activity based on the structure-based virtual screening.

Sejong University

18358718

Discovery of novel PRL-3 inhibitors based on the structure-based virtual screening.

Sejong University

17379514

Fluorinated NSC as a Cdc25 inhibitor.

Sejong University

27676184

Application of Fragment-Based de Novo Design to the Discovery of Selective Picomolar Inhibitors of Glycogen Synthase Kinase-3 Beta.

Sejong University