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
122584-83-2
15944-74-8
1635-61-6
17700-09-3
26196-45-2
3209-22-1
351019-18-6 | 6-Fluoropyridine-3-boronic acid | AA003394 | MFCD03411559
96-96-8 | 4-Methoxy-2-nitroaniline | AA0033BZ | MFCD00007152
606-83-7 | 3,3-Diphenylpropionic acid | AA0033EZ | MFCD00002717
34552-14-2 | 3-Amino-2-bromo-5-picoline | AA0033HW | MFCD08277281
1871-57-4 | 3-Chloro-2-(chloromethyl)prop-1-ene | AA0033KK | MFCD00000952
109-78-4 | 3-Hydroxypropionitrile | AA0033NH | MFCD00002826
73870-24-3 | 4-(Bromomethyl)pyridine hydrobromide | AA0033QG | MFCD01863545
2789-25-5 | 4-Amino-2-chloro-3-nitropyridine | AA0033TB | MFCD07368898
771583-81-4 | 4-Chloro-2-(trifluoromethyl)benzylamine | AA0033W9 | MFCD06213291
145370-39-4 | 2-(3-Methoxy-4-nitrophenyl)-4h-chromen-4-one | AA0033Z0 | MFCD22479198