The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27020306 |
18 |
Discovery of KDM5A inhibitors: Homology modeling, virtual screening and structure-activity relationship analysis. |
Sichuan University |
26710088 |
248 |
Recent Progress in Histone Demethylase Inhibitors. |
University Of Oxford |
26985284 |
30 |
Inhibition of Histone Demethylases Offers a Novel and Promising Approach for the Treatment of Cancer and Other Diseases. |
Therachem Research Medilab (India) |
26699912 |
108 |
Docking and Linking of Fragments To Discover Jumonji Histone Demethylase Inhibitors. |
University Of Oxford |
26741168 |
239 |
8-Substituted Pyrido[3,4-d]pyrimidin-4(3H)-one Derivatives As Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors. |
The Institute Of Cancer Research |
| 12 |
Calorimetric Studies on the Complexation of Several Ferrocene Derivatives by .alpha.- and .beta.-Cyclodextrin. Effects of Urea on the Thermodynamic Parameters |
University Of Miami |
19168353 |
25 |
Discovery and SAR of para-alkylthiophenoxyacetic acids as potent and selective PPARdelta agonists. |
Johnson & Johnson Pharmaceutical |
19237286 |
30 |
Design of potent thiophene inhibitors of polo-like kinase 1 with improved solubility and reduced protein binding. |
Gsk |
19217287 |
30 |
Development of multitargeted inhibitors of both the insulin-like growth factor receptor (IGF-IR) and members of the epidermal growth factor family of receptor tyrosine kinases. |
Abbott Laboratories |
19260677 |
11 |
Structure-activity relationships of orotidine-5'-monophosphate decarboxylase inhibitors as anticancer agents. |
Toronto General Research Institute |
18054488 |
24 |
Novel thiol-based TACE inhibitors. Part 2: Rational design, synthesis, and SAR of thiol-containing aryl sulfones. |
Vertex Pharmaceuticals |
18640037 |
48 |
Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studies. |
Universita Degli Studi Di Firenze |
18729351 |
21 |
Potent cationic inhibitors of West Nile virus NS2B/NS3 protease with serum stability, cell permeability and antiviral activity. |
University Of Queensland |
14998327 |
12 |
Structure-based optimization of novel azepane derivatives as PKB inhibitors. |
Roche Diagnostics |
11708928 |
17 |
Role of hydrophilic interaction in binding of hydroxylated 3-deoxy C(19) steroids to the active site of aromatase. |
Tohoku Pharmaceutical University |
28841282 |
2 |
Synthetic Lethality Triggered by Combining Olaparib with BRCA2-Rad51 Disruptors. |
Istituto Italiano Di Tecnologia |