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Results: 1-17 |
Results: 17
An anthelmintic compound, nafuredin, shows selective inhibition of complexI in helminth mitochondria
Authors: Omura, S Miyadera, H Ui, H Shiomi, K Yamaguchi, Y Masuma, R Nagamitsu, T Takano, D Sunazuka, T Harder, A Kolbl, H Namikoshi, M Miyoshi, H Sakamoto, K Kita, K
Citation: S. Omura et al., An anthelmintic compound, nafuredin, shows selective inhibition of complexI in helminth mitochondria, P NAS US, 98(1), 2001, pp. 60-62
Convergent synthesis of arisugacin skeletons and their acetylcholinesterase inhibitory activity
Authors: Handa, M Sunazuka, T Nagai, K Kimura, R Shirahata, T Tian, ZM Otoguro, K Harigaya, Y Omura, S
Citation: M. Handa et al., Convergent synthesis of arisugacin skeletons and their acetylcholinesterase inhibitory activity, J ANTIBIOT, 54(4), 2001, pp. 382-385
Determination of absolute stereochemistries of arisugacin F and territrem B, novel acetylcholinesterase inhibitors
Authors: Handa, M Sunazuka, T Nagai, R Kimura, R Otoguro, K Harigaya, Y Omura, S
Citation: M. Handa et al., Determination of absolute stereochemistries of arisugacin F and territrem B, novel acetylcholinesterase inhibitors, J ANTIBIOT, 54(4), 2001, pp. 386-391
Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554
Authors: Ui, H Shiomi, K Yamaguchi, Y Masuma, R Nagamitsu, T Takano, D Sunazuka, T Namikoshi, M Omura, S
Citation: H. Ui et al., Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554, J ANTIBIOT, 54(3), 2001, pp. 234-238
Synthetic conversion of ACAT inhibitor to acetylcholinesterase inhibitor
Authors: Obata, R Sunazuka, T Otoguro, K Tomoda, H Harigaya, Y Omura, S
Citation: R. Obata et al., Synthetic conversion of ACAT inhibitor to acetylcholinesterase inhibitor, BIOORG MED, 10(12), 2000, pp. 1315-1316
Total syntheses of kurasoins A and B, novel protein farnesyltransferase inhibitors, and absolute structures of kurasoins A and B
Authors: Hirose, T Sunazuka, T Tian, ZM Handa, M Uchida, R Shiomi, K Harigaya, Y Omura, S
Citation: T. Hirose et al., Total syntheses of kurasoins A and B, novel protein farnesyltransferase inhibitors, and absolute structures of kurasoins A and B, HETEROCYCLE, 53(4), 2000, pp. 777-784
The efficient total synthesis of bioactive microbial natural products
Authors: Sunazuka, T
Citation: T. Sunazuka, The efficient total synthesis of bioactive microbial natural products, J SYN ORG J, 58(9), 2000, pp. 828-838
Structure-activity relationships study of pyripyropenes: Reversal of cancer cell multidrug resistance
Authors: Obata, R Sunazuka, T Harigaya, Y Hayashi, M Rho, MC Tomoda, H Omura, S
Citation: R. Obata et al., Structure-activity relationships study of pyripyropenes: Reversal of cancer cell multidrug resistance, J ANTIBIOT, 53(4), 2000, pp. 422-425
Synthesis and antiangiogenic activity of staurosporine derivatives
Authors: Li, ZR Sunazuka, T Yamada, R Kato, Y Enomoto, A Hayashi, M Harigaya, Y Omura, S
Citation: Zr. Li et al., Synthesis and antiangiogenic activity of staurosporine derivatives, J ANTIBIOT, 53(4), 2000, pp. 426-429
Reversal of multidrug resistance by 7-O-benzoylpyripyropene A in multidrug-resistant tumor cells
Authors: Rho, MC Hayashi, M Fukami, A Obata, R Sunazuka, T Tomoda, H Komiyama, K Omura, S
Citation: Mc. Rho et al., Reversal of multidrug resistance by 7-O-benzoylpyripyropene A in multidrug-resistant tumor cells, J ANTIBIOT, 53(10), 2000, pp. 1201-1206
Effect of 14-membered ring macrolide compounds on rat leucocyte chemotaxisand the structure-activity relationships
Authors: Oohori, M Otoguro, K Sunazuka, T Kunihiko, S Iwai, Y Omura, S
Citation: M. Oohori et al., Effect of 14-membered ring macrolide compounds on rat leucocyte chemotaxisand the structure-activity relationships, J ANTIBIOT, 53(10), 2000, pp. 1219-1222
Arisugacins C and D, novel acetylcholinesterase inhibitors and their related novel metabolites produced by Penicillium sp FO-4259-11
Authors: Otoguro, K Shiomi, K Yamaguchi, Y Arai, N Sunazuka, T Masuma, R Iwai, Y Omura, S
Citation: K. Otoguro et al., Arisugacins C and D, novel acetylcholinesterase inhibitors and their related novel metabolites produced by Penicillium sp FO-4259-11, J ANTIBIOT, 53(1), 2000, pp. 50-57
Three-dimensional structure-activity relationship analysis between motilinand motilide using conformational analysis and a novel molecular superposing method
Authors: Gouda, H Sunazuka, T Omura, S Hirono, S
Citation: H. Gouda et al., Three-dimensional structure-activity relationship analysis between motilinand motilide using conformational analysis and a novel molecular superposing method, CHEM PHARM, 48(11), 2000, pp. 1835-1837
Erythromycin suppresses nuclear factor-kappa B and activator protein-1 activation in human bronchial epithelial cells
Authors: Desaki, M Takizawa, H Ohtoshi, T Kasama, T Kobayashi, K Sunazuka, T Omura, S Yamamoto, K Ito, K
Citation: M. Desaki et al., Erythromycin suppresses nuclear factor-kappa B and activator protein-1 activation in human bronchial epithelial cells, BIOC BIOP R, 267(1), 2000, pp. 124-128
Effecting and measuring risk reduction in software development
Authors: Greer, D Bustard, DW Sunazuka, T
Citation: D. Greer et al., Effecting and measuring risk reduction in software development, NEC RES DEV, 40(3), 1999, pp. 378-383
Effects of erythromycin and its derivatives on interleukin-8 release by human bronchial epithelial cell line BEAS-2B cells
Authors: Sunazuka, T Takizawa, H Desaki, M Suzuki, K Obata, R Otoguro, K Omura, S
Citation: T. Sunazuka et al., Effects of erythromycin and its derivatives on interleukin-8 release by human bronchial epithelial cell line BEAS-2B cells, J ANTIBIOT, 52(1), 1999, pp. 71-74
Differential inhibition of HMG-CoA synthase and pancreatic lipase by the specific chiral isomers of beta-lactone DU-6622
Authors: Tomoda, H Ohbayashi, N Kumagai, H Hashizume, H Sunazuka, T Omura, S
Citation: H. Tomoda et al., Differential inhibition of HMG-CoA synthase and pancreatic lipase by the specific chiral isomers of beta-lactone DU-6622, BIOC BIOP R, 265(2), 1999, pp. 536-540
Risultati: 1-17 |