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| PMID | Data | Article Title | Citation | Organization | Data Download |
|---|---|---|---|---|---|
| 19902958 | 24 | Solid phase synthesis of novel pyrrolidinedione analogs as potent HIV-1 integrase inhibitors. | J Comb Chem 12: 84-90 (2010) | Bristol-Myers Squibb Co. | 2D 3D TSV |
| 20349953 | 49 | Solution phase parallel synthesis of substituted 3-phenylsulfonyl-[1,2,3]triazolo[1,5-a]quinazolines: selective serotonin 5-HT(6) receptor antagonists. | J Comb Chem 12: 445-52 (2010) | Chemical Diversity Research Institute | 2D 3D TSV |
| 20518551 | 10 | One-pot synthesis of 4,6-diaryl-2-oxo(imino)-1,2-dihydropyridine-3-carbonitrile; a New Scaffold for p38alpha MAP kinase inhibition. | J Comb Chem 12: 559-65 (2010) | German University in Cairo | 2D 3D TSV |
| 20666436 | 56 | Dipeptidyl-quinolone derivatives inhibit hypoxia inducible factor-1a prolyl hydroxylases-1, -2, and -3 with altered selectivity. | J Comb Chem 12: 676-86 (2010) | Amgen Inc | 2D 3D TSV |
| 20578711 | 19 | Solution phase synthesis of a combinatorial library of chalcones and flavones as potent cathepsin V inhibitors. | J Comb Chem 12: 687-95 (2010) | Universidade Federal de São Carlo | 2D 3D TSV |