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Results: 1-18 |
Results: 18
Synthesis and structure-activity relationships of potent and orally activesulfonamide ETB selective antagonists
Authors: Kanda, Y Kawanishi, Y Oda, K Sakata, T Mihara, S Asakura, K Kanemasa, T Ninomiya, M Fujimoto, M Konoike, T
Citation: Y. Kanda et al., Synthesis and structure-activity relationships of potent and orally activesulfonamide ETB selective antagonists, BIO MED CH, 9(4), 2001, pp. 897-907
Design, synthesis and pharmacological evaluation of 3-benzylazetidine-2-one-based human chymase inhibitors
Authors: Aoyama, Y Uenaka, M Kii, M Tanaka, M Konoike, T Hayasaki-Kajiwara, Y Naya, N Nakajima, M
Citation: Y. Aoyama et al., Design, synthesis and pharmacological evaluation of 3-benzylazetidine-2-one-based human chymase inhibitors, BIO MED CH, 9(11), 2001, pp. 3065-3075
Synthesis and structure-activity relationships of a new class of 1-oxacephem-based human chymase inhibitors (vol 11, pg 2397, 2001)
Authors: Aoyama, Y Uenaka, M Konoike, T Iso, Y Nishitani, Y Kanda, A Naya, N Nakajima, M
Citation: Y. Aoyama et al., Synthesis and structure-activity relationships of a new class of 1-oxacephem-based human chymase inhibitors (vol 11, pg 2397, 2001), BIOORG MED, 11(15), 2001, pp. 2055-2055
Inhibition of serine proteases: Activity of 1,3-diazetidine-2,4-diones
Authors: Aoyama, Y Uenaka, M Konoike, T Hayasaki-Kajiwara, Y Naya, N Nakajima, M
Citation: Y. Aoyama et al., Inhibition of serine proteases: Activity of 1,3-diazetidine-2,4-diones, BIOORG MED, 11(13), 2001, pp. 1691-1694
Total synthesis of human chymase inhibitor methyllinderone and structure-activity relationships of its derivatives
Authors: Aoyama, Y Konoike, T Kanda, A Naya, N Nakajima, M
Citation: Y. Aoyama et al., Total synthesis of human chymase inhibitor methyllinderone and structure-activity relationships of its derivatives, BIOORG MED, 11(13), 2001, pp. 1695-1697
Stereoselective total synthesis of (-)-alpha-eudesmol, a P/Q-type calcium channel blocker
Authors: Aoyama, Y Araki, Y Konoike, T
Citation: Y. Aoyama et al., Stereoselective total synthesis of (-)-alpha-eudesmol, a P/Q-type calcium channel blocker, SYNLETT, (9), 2001, pp. 1452-1454
Efficient synthesis of EDO-S,S-DMEDT-TTF, a potent organic-donor for synthetic metals
Authors: Konoike, T Namba, K Shinada, T Sakaguchi, K Papavassiliou, GC Murata, K Ohfune, Y
Citation: T. Konoike et al., Efficient synthesis of EDO-S,S-DMEDT-TTF, a potent organic-donor for synthetic metals, SYNLETT, (9), 2001, pp. 1476-1478
Preparation, structure and physical properties of some new organic conductors of tau-phase
Authors: Papavassiliou, GC Mousdis, GA Terzis, A Raptopoulou, C Murata, K Konoike, T Yoshino, Y
Citation: Gc. Papavassiliou et al., Preparation, structure and physical properties of some new organic conductors of tau-phase, SYNTH METAL, 120(1-3), 2001, pp. 743-744
Low temperature electric nature of tau-phase conductors
Authors: Konoike, T Oda, A Iwashita, K Yamamoto, T Tajima, H Yoshino, H Ueda, K Sugimoto, T Hiraki, K Takahashi, T Sasaki, T Nishio, Y Kajita, K Papavassiliou, GC Mousdis, GA Murata, K
Citation: T. Konoike et al., Low temperature electric nature of tau-phase conductors, SYNTH METAL, 120(1-3), 2001, pp. 801-802
Effect of microstructure on reliability of Ca(TiZr)O-3-based multilayer ceramic capacitors
Authors: Motoki, T Naito, M Sano, H Konoike, T Tomono, K
Citation: T. Motoki et al., Effect of microstructure on reliability of Ca(TiZr)O-3-based multilayer ceramic capacitors, JPN J A P 1, 39(9B), 2000, pp. 5565-5568
Synthesis and structure-activity relationships of a new class of 1-oxacephem-based human chymase inhibitors
Authors: Aoyama, Y Uenaka, M Konoike, T Iso, Y Nishitani, Y Kanda, A Naya, N Nakajima, M
Citation: Y. Aoyama et al., Synthesis and structure-activity relationships of a new class of 1-oxacephem-based human chymase inhibitors, BIOORG MED, 10(21), 2000, pp. 2397-2401
1-Oxacephem-based human chymase inhibitors: Discovery of stable inhibitorsin human plasma
Authors: Aoyama, Y Uenaka, M Konoike, T Iso, Y Nishitani, Y Kanda, A Naya, N Nakajima, M
Citation: Y. Aoyama et al., 1-Oxacephem-based human chymase inhibitors: Discovery of stable inhibitorsin human plasma, BIOORG MED, 10(21), 2000, pp. 2403-2406
Discovery and synthesis of a potent sulfonamide ETB selective antagonist
Authors: Kanda, Y Takahashi, T Araki, Y Konoike, T Mihara, S Fujimoto, M
Citation: Y. Kanda et al., Discovery and synthesis of a potent sulfonamide ETB selective antagonist, BIOORG MED, 10(16), 2000, pp. 1875-1878
Olefin formation by deoxystannylation
Authors: Araki, Y Konoike, T
Citation: Y. Araki et T. Konoike, Olefin formation by deoxystannylation, J SYN ORG J, 58(10), 2000, pp. 956-965
BaTiO3-based non-reducible low-loss dielectric ceramics
Authors: Nakamura, T Sano, H Konoike, T Tomono, K
Citation: T. Nakamura et al., BaTiO3-based non-reducible low-loss dielectric ceramics, JPN J A P 1, 38(9B), 1999, pp. 5457-5460
Practical large-scale synthesis of endothelin receptor antagonist S-0139
Authors: Konoike, T Oda, K Uenaka, M Takahashi, K
Citation: T. Konoike et al., Practical large-scale synthesis of endothelin receptor antagonist S-0139, ORG PROC R, 3(5), 1999, pp. 347-351
A novel allylic hydroxylation of sterically hindered olefins by Fe-porphyrin-catalyzed mCPBA oxidation
Authors: Konoike, T Araki, Y Kanda, Y
Citation: T. Konoike et al., A novel allylic hydroxylation of sterically hindered olefins by Fe-porphyrin-catalyzed mCPBA oxidation, TETRAHEDR L, 40(38), 1999, pp. 6971-6974
Synthesis of [2-C-13]-oleanolic acid and [2-C-13]-myricerone
Authors: Konoike, T Takahashi, K Kitaura, Y Kanda, Y
Citation: T. Konoike et al., Synthesis of [2-C-13]-oleanolic acid and [2-C-13]-myricerone, TETRAHEDRON, 55(52), 1999, pp. 14901-14914
Risultati: 1-18 |