The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28105287 |
19 |
Systematic Study of Effects of Structural Modifications on the Aqueous Solubility of Drug-like Molecules. |
Yale University |
27156768 |
18 |
Irregularities in enzyme assays: The case of macrophage migration inhibitory factor. |
Yale University |
25743213 |
52 |
Multiple binding modes of isothiocyanates that inhibit macrophage migration inhibitory factor. |
University of Otago |
24712915 |
14 |
Discovery of novel inhibitors targeting the macrophage migration inhibitory factor via structure-based virtual screening and bioassays. |
Zhejiang University |
23067344 |
34 |
Virtual screening and optimization yield low-nanomolar inhibitors of the tautomerase activity of Plasmodium falciparum macrophage migration inhibitory factor. |
Yale University |
20639113 |
23 |
An integrative in silico methodology for the identification of modulators of macrophage migration inhibitory factor (MIF) tautomerase activity. |
Brain Mind Institute |
17526494 |
12 |
Alternative chemical modifications reverse the binding orientation of a pharmacophore scaffold in the active site of macrophage migration inhibitory factor. |
Yale University |
11170644 |
18 |
Coumarin and chromen-4-one analogues as tautomerase inhibitors of macrophage migration inhibitory factor: discovery and X-ray crystallography. |
Yamanouchi Pharmaceutical |
22088307 |
10 |
Synthesis and bio-evaluation of human macrophage migration inhibitory factor inhibitor to develop anti-inflammatory agent. |
Institute of Chemical Biology |
21719283 |
25 |
Benzisothiazolones as modulators of macrophage migration inhibitory factor. |
Yale University |
20971005 |
10 |
Receptor agonists of macrophage migration inhibitory factor. |
Yale University |
20728358 |
11 |
Optimization of N-benzyl-benzoxazol-2-ones as receptor antagonists of macrophage migration inhibitory factor (MIF). |
Yale University |
20185308 |
1 |
Fragment screening of inhibitors for MIF tautomerase reveals a cryptic surface binding site. |
Sanofi-Aventis |
19592246 |
54 |
Novel derivatives of ISO-1 as potent inhibitors of MIF biological function. |
Piramal Life Sciences |
19090668 |
31 |
Discovery of human macrophage migration inhibitory factor (MIF)-CD74 antagonists via virtual screening. |
Yale University |
17385848 |
15 |
Phenolic hydrazones are potent inhibitors of macrophage migration inhibitory factor proinflammatory activity and survival improving agents in sepsis. |
The New York School of Medicine |
16682188 |
22 |
Critical modifications of the ISO-1 scaffold improve its potent inhibition of macrophage migration inhibitory factor (MIF) tautomerase activity. |
Institute For Medical Research |
16420039 |
5 |
Classification of chemical compounds by protein-compound docking for use in designing a focused library. |
National Institute of Advanced Industrial Science and Technology (Aist) |
12036350 |
9 |
Inhibition of MIF bioactivity by rational design of pharmacological inhibitors of MIF tautomerase activity. |
Institute For Medical Research |
23659282 |
1 |
Spirohexenolide A targets human macrophage migration inhibitory factor (hMIF). |
University of California-San Diego |
29812929 |
34 |
Advances and Insights for Small Molecule Inhibition of Macrophage Migration Inhibitory Factor. |
Yale University |
29428527 |
9 |
Discovery of chromenes as inhibitors of macrophage migration inhibitory factor. |
University of Groningen |
29259749 |
24 |
Adding a Hydrogen Bond May Not Help: Naphthyridinone vs Quinoline Inhibitors of Macrophage Migration Inhibitory Factor. |
Yale University |
29526099 |
5 |
Design, Synthesis, and Biological Activity of New N-(Phenylmethyl)-benzoxazol-2-thiones as Macrophage Migration Inhibitory Factor (MIF) Antagonists: Efficacies in Experimental Pulmonary Hypertension. |
Hospital Marie Lannelongue |
27235003 |
10 |
PXD101 analogs with L-phenylglycine-containing branched cap as histone deacetylase inhibitors. |
Shandong University |
| 31 |
Novel 2(3H)-benzothiazolones as highly potent and selective sigma-1 receptor ligands |
Universite De Lille |