AAAAAA

   
Results: 1-8 |
Results: 8
Synthesis of nodulisporic acid 2 ''-oxazoles and 2 ''-thiazoles
Authors: Berger, R Shoop, WL Pivnichny, JV Warmke, LM Zakson-Aiken, M Owens, KA deMontigny, P Schmatz, DM Wyvratt, MJ Fisher, MH Meinke, PT Colletti, SL
Citation: R. Berger et al., Synthesis of nodulisporic acid 2 ''-oxazoles and 2 ''-thiazoles, ORG LETT, 3(23), 2001, pp. 3715-3718
Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1
Authors: Colletti, SL Myers, RW Darkin-Rattray, SJ Gurnett, AM Dulski, PM Galuska, S Allocco, JJ Ayer, MB Li, CS Lim, J Crumley, TM Cannova, C Schmatz, DM Wyvratt, MJ Fisher, MH Meinke, PT
Citation: Sl. Colletti et al., Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 1, BIOORG MED, 11(2), 2001, pp. 107-111
Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 2
Authors: Colletti, SL Myers, RW Darkin-Rattray, SJ Gurnett, AM Dulski, PM Galuska, S Allocco, JJ Ayer, MB Li, CS Lim, J Crumley, TM Cannova, C Schmatz, DM Wyvratt, MJ Fisher, MH Meinke, PT
Citation: Sl. Colletti et al., Broad spectrum antiprotozoal agents that inhibit histone deacetylase: Structure-activity relationships of apicidin. Part 2, BIOORG MED, 11(2), 2001, pp. 113-117
Chemical modification of nodulisporic acid A: Preliminary structure-activity relationships
Authors: Meinke, PT Ayer, MB Colletti, SL Li, CS Lim, J Ok, D Salva, S Schmatz, DM Shih, TL Shoop, WL Warmke, LM Wyvratt, MJ Zakson-Aiken, M Fisher, MH
Citation: Pt. Meinke et al., Chemical modification of nodulisporic acid A: Preliminary structure-activity relationships, BIOORG MED, 10(20), 2000, pp. 2371-2374
Tryptophan-replacement and indole-modifed apicidins: synthesis of potent and selective antiprotozoal agents
Authors: Colletti, SL Li, CS Fisher, MH Wyvratt, MJ Meinke, PT
Citation: Sl. Colletti et al., Tryptophan-replacement and indole-modifed apicidins: synthesis of potent and selective antiprotozoal agents, TETRAHEDR L, 41(41), 2000, pp. 7825-7829
Synthesis of side chain modified apicidin derivatives: potent mechanism-based histone deacetylase inhibitors
Authors: Meinke, PT Colletti, SL Ayer, MB Darkin-Rattray, SJ Myers, RW Schmatz, DM Wyvratt, MJ Fisher, MH
Citation: Pt. Meinke et al., Synthesis of side chain modified apicidin derivatives: potent mechanism-based histone deacetylase inhibitors, TETRAHEDR L, 41(41), 2000, pp. 7831-7835
Design and synthesis of histone deacetylase inhibitors: the development ofapicidin transition state analogs
Authors: Colletti, SL Myers, RW Darkin-Rattray, SJ Schmatz, DM Fisher, MH Wyvratt, MJ Meinke, PT
Citation: Sl. Colletti et al., Design and synthesis of histone deacetylase inhibitors: the development ofapicidin transition state analogs, TETRAHEDR L, 41(41), 2000, pp. 7837-7841
Synthesis of apicidin-derived quinolone derivatives: Parasite-selective histone deacetylase inhibitors and antiproliferative agents
Authors: Meinke, PT Colletti, SL Doss, G Myers, RW Gurnett, AM Dulski, PM Darkin-Rattray, SJ Allocco, JJ Galuska, S Schmatz, DM Wyvratt, MJ Fisher, MH
Citation: Pt. Meinke et al., Synthesis of apicidin-derived quinolone derivatives: Parasite-selective histone deacetylase inhibitors and antiproliferative agents, J MED CHEM, 43(25), 2000, pp. 4919-4922
Risultati: 1-8 |