Title: One scaffold, three binding modes: novel and selective pteridine reductase 1 inhibitors derived from fragment hits discovered by virtual screening.
Journal: Journal of medicinal chemistry 20090723
62054-67-5 | Ths-044 | AA00ECCZ | MFCD29472287
60792-56-5 | 2-(1H-Benzoimidazol-2-yl)-acetamide | AA00ECHA | MFCD00223123
61826-76-4 | (S)-3-Phenoxybenzaldehyde cyanohydrin | AA00ECMQ | MFCD01937336
58666-08-3 | Ethyl 4,7-dichloro-8-methylquinoline-3-carboxylate | AA00ECTS | MFCD00173378
64114-29-0 | 2-(Bromomethyl)-6-methylpyridine hydrobromide | AA00ED1G | MFCD08436135
628692-17-1 | 1-Benzothien-7-ylboronic acid | AA00ED8F | MFCD06740320
57229-67-1 | Boc-trp-obzl | AA00EDIB | MFCD00190837
590353-07-4 | 5-(2-Cyclohexylethyl)-4-ethyl-4h-1,2,4-triazole-3-thiol | AA00EDPN | MFCD03945669
59736-34-4 | 2-Cyano-n-(2-methylphenyl)acetamide | AA00EDTL | MFCD00816893
588676-14-6 | 8-Chloro-2-(5-methyl-2-furyl)quinoline-4-carboxylic acid | AA00EDY6 | MFCD03422171