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Results: 1-8 |
Results: 8
Ring closing metathesis mediated synthesis of 4a-aryloxodecahydroisoquinolines, intermediates in the preparation of novel opiates
Authors: Liras, S Allen, MP Blake, JF
Citation: S. Liras et al., Ring closing metathesis mediated synthesis of 4a-aryloxodecahydroisoquinolines, intermediates in the preparation of novel opiates, ORG LETT, 3(22), 2001, pp. 3483-3486
Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: Structure-activity relationship of the C-2 side chain tether
Authors: Chenard, BL Welch, WM Blake, JF Butler, TW Reinhold, A Ewing, FE Menniti, FS Pagnozzi, MJ
Citation: Bl. Chenard et al., Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: Structure-activity relationship of the C-2 side chain tether, J MED CHEM, 44(11), 2001, pp. 1710-1717
Prague territories: National conflict and cultural innovation in Franz Kafka's fin-de-siecle
Authors: Blake, JF
Citation: Jf. Blake, Prague territories: National conflict and cultural innovation in Franz Kafka's fin-de-siecle, GER REV, 76(1), 2001, pp. 92-95
Design, synthesis and biological evaluation of 3-amino-3-phenylpropionamide derivatives as novel mu opioid receptor ligands
Authors: Allen, MP Blake, JF Bryce, DK Haggan, ME Liras, S McLean, S Segelstein, BE
Citation: Mp. Allen et al., Design, synthesis and biological evaluation of 3-amino-3-phenylpropionamide derivatives as novel mu opioid receptor ligands, BIOORG MED, 10(6), 2000, pp. 523-526
Chemoinformatics - predicting the physicochemical properties of 'drug-like' molecules
Authors: Blake, JF
Citation: Jf. Blake, Chemoinformatics - predicting the physicochemical properties of 'drug-like' molecules, CURR OPIN B, 11(1), 2000, pp. 104-107
Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold
Authors: Robinson, RP Laird, ER Blake, JF Bordner, J Donahue, KM Lopresti-Morrow, LL Mitchell, PG Reese, MR Reeves, LM Stam, EJ Yocum, SA
Citation: Rp. Robinson et al., Structure-based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold, J MED CHEM, 43(12), 2000, pp. 2293-2296
Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S-2 pocket
Authors: Reiter, LA Rizzi, JP Pandit, J Lasut, MJ McGahee, SM Parikh, VD Blake, JF Danley, DE Laird, ER Lopez-Anaya, A Lopresti-Morrow, LL Mansour, MN Martinelli, GJ Mitchell, PG Owens, BS Pauly, TA Reeves, LM Schulte, GK Yocum, SA
Citation: La. Reiter et al., Inhibition of MMP-1 and MMP-13 with phosphinic acids that exploit binding in the S-2 pocket, BIOORG MED, 9(2), 1999, pp. 127-132
Inclusion complexation of ziprasidone mesylate with beta-cyclodextrin sulfobutyl ether
Authors: Kim, Y Oksanen, DA Massefski, W Blake, JF Duffy, EM Chrunyk, B
Citation: Y. Kim et al., Inclusion complexation of ziprasidone mesylate with beta-cyclodextrin sulfobutyl ether, J PHARM SCI, 87(12), 1998, pp. 1560-1567
Risultati: 1-8 |