The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 25221666 |
20 |
Acyclic tethers mimicking subunits of polysaccharide ligands: selectin antagonists. |
Institut De Recherches Cliniques De Montr£Al (Ircm) |
| 17004713 |
3 |
A novel class of potent nonglycosidic and nonpeptidic pan-selectin inhibitors. |
Johannes Gutenberg University |
| 17845854 |
2 |
Is adamantane a suitable substituent to pre-organize the acid orientation in E-selectin antagonists? |
University of Basel |
| 17302397 |
113 |
Rational design of novel, potent small molecule pan-selectin antagonists. |
Revotar Biopharmaceuticals |
| 11563928 |
2 |
Synthesis and biological evaluation of sialylmimetics as rotavirus inhibitors. |
Griffith University (Gold Coast Campus) |
| 11405647 |
24 |
Development of potent non-carbohydrate imidazole-based small molecule selectin inhibitors with antiinflammatory activity. |
Ontogen |
| 10780903 |
6 |
Study on selectin blocker. 8. Lead discovery of a non-sugar antagonist using a 3D-pharmacophore model. |
Nippon Organon K.K. |
| 9544210 |
46 |
Novel synthetic inhibitors of selectin-mediated cell adhesion: synthesis of 1,6-bis[3-(3-carboxymethylphenyl)-4-(2-alpha-D- mannopyranosyloxy)phenyl]hexane (TBC1269). |
Texas Biotechnology |
| 9784103 |
42 |
Studies on selectin blockers. 7. Structure-activity relationships of sialyl Lewis X mimetics based on modified Ser-Glu dipeptides. |
Kanebo |
| 9632363 |
5 |
Studies on selectin blockers. 6. Discovery of homologous fucose sugar unit necessary for E-selectin binding. |
Kanebo |
| 9357520 |
18 |
Studies on selection blockers. 5. Design, synthesis, and biological profile of sialyl Lewis x mimetics based on modified serine-glutamic acid dipeptides. |
Kanebo |
| 8632441 |
24 |
Studies on selectin blocker. 1. Structure-activity relationships of sialyl Lewis X analogs. |
Institute of Cancer Research |
| 8642564 |
12 |
Studies on selectin blockers. 2. Novel selectin blocker as potential therapeutics for inflammatory disorders. |
New Drug Research Laboratory |
| 8544173 |
37 |
Rational design and synthesis of small molecule, non-oligosaccharide selectin inhibitors: (alpha-D-mannopyranosyloxy)biphenyl-substituted carboxylic acids. |
Texas Biotechnology |
| 11354355 |
6 |
Design and synthesis of a new sialyl Lewis X mimetic: how selective are the selectin receptors? |
Universit£ |
| 11229747 |
10 |
Synthesis of sialyl Lewis(x) mimics. Modifications of the 6-position of galactose. |
Novartis Pharma |
| 11206447 |
12 |
Design and synthesis of sialyl Lewis x mimics as E-selectin inhibitors. |
Wyeth Research |
| 11412987 |
2 |
Synthesis of novel sialylmimetics as biological probes. |
Monash University (Parkville Campus) |
| 10969978 |
9 |
A solid-phase synthesis for beta-turn mimetics of sialyl Lewis X. |
Nippon Organon K.K. |
| 9873626 |
1 |
Exploration of beta-turn scaffolding motifs as components of sialyl Le(X) mimetics and their relevance to P-selectin. |
Universit£ |
| 9873537 |
71 |
Synthesis of sialyl Lewis X mimetics using the Ugi four-component reaction. |
Scripps Research Institute |
| | 8 |
Synthesis and inhibitory effects of bivalent sialyl lewis X analogs at preventing cell adhesion |
TBA |
| | 5 |
Synthesis and biological activity of conformationally constrained sialyl Lewis X analogues with reduced carbohydrate character |
TBA |
| | 12 |
Liposome-like fucopeptides as sialyl lewis X mimetics |
TBA |
| | 2 |
Spiroketal glycomimetics: the synthesis of a conformationally restrained Sialyl Lewis X mimic |
TBA |
| 20171887 |
15 |
Synthesis of fluorinated C-mannopeptides as sialyl Lewisx mimics for E- and P-selectin inhibition. |
Universit£ |
| | 8 |
Chemical and enzymatic synthesis of high-affinity selectin ligands |
TBA |
| | 1 |
Glycomimetic selectin inhibitors: (α-D-mannopyranosyloxy)methylbiphenyls |
TBA |
| | 13 |
Synthesis and biological activity of novel sialyl-lewisX conjugates |
TBA |
| | 6 |
Stereoselective synthesis of lewis-associated trisaccharides as E-selectin inhibitors |
TBA |
| 15936191 |
16 |
Sialyl Lewis(x) analogs based on a quinic acid scaffold as the fucose mimic. |
National Chemical Engineering Institute In Paris |
| 11585452 |
291 |
Selective inhibition of ICAM-1 and E-selectin expression in human endothelial cells. 2. Aryl modifications of 4-(aryloxy)thieno[2,3-c]pyridines with fine-tuning at C-2 carbamides. |
Abbott Laboratories |
| 11300880 |
168 |
Discovery of inhibitors of cell adhesion molecule expression in human endothelial cells. 1. Selective inhibition of ICAM-1 and E-selectin expression. |
Abbott Laboratories |
| 11294392 |
3 |
Synthesis and biological evaluation of a sialyl Lewis X mimic with significantly improved E-selectin inhibition. |
Novartis Pharma |
| 10579852 |
8 |
Synthesis and biological evaluation of a potent E-selectin antagonist. |
Novartis Pharma |
| 9873724 |
21 |
Aryl C-glycosides: physiologically stable glycomimetics of sialyl Lewis X. |
Sankyo |
| 9873622 |
1 |
Sialyl Lewis X-polysaccharide conjugates: targeting inflammatory lesions. |
Drug Delivery System Institute |
| 9022803 |
9 |
Selectin-ligand interactions revealed by molecular dynamics simulation in solution. |
Kanebo |
| 8691465 |
4 |
Ligand interactions with E-selectin. Identification of a new binding site for recognition of N-acyl aromatic glucosamine substituents of sialyl Lewis X. |
Cytel |
| 8145218 |
8 |
3-Alkoxybenzo[b]thiophene-2-carboxamides as inhibitors of neutrophil-endothelial cell adhesion. |
Warner-Lambert |
| 7523674 |
1 |
Structure--activity relationships of sialyl Lewis x-containing oligosaccharides. 1. Effect of modifications of the fucose moiety. |
Cytel |
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