Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mayumi Uesugi"'
Autor:
Atsuko Fukunaga, Kyoko Nakanishi, Atsuko Miyajima, Yoshiko Tamura-Horikawa, Shigeki Tamura, Mayumi Uesugi, Hirokazu Annoura
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:2999-3002
A series of novel arylpiperidines (4a-d) which have highly potent blocking effects for both neuronal Na+ and T-type Ca2+ channels with extremely low affinity for dopamine D2 receptors were synthesized. Among these compounds, 1-(2-hydroxy-3-phenoxy)pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8919444126f63fec2c74290be340a423
https://doi.org/10.1016/s0960-894x(99)00516-8
https://doi.org/10.1016/s0960-894x(99)00516-8
Autor:
Taylor Merry, Selvi Pradeepan, Raji Sundaramoorthi, Virginia A. Jacobsen, Mayumi Uesugi, Vaibhav Varkhedkar, Chi B. Vu, Chester A. Metcalf, Jeremy Green, Dennis A. Holt, Edgardo Laborde, Karina J. Macek, Yinka Green
Publikováno v:
Tetrahedron Letters. 39:3435-3438
An efficient method for the preparation of protected phosphate ester-linked resins in high yield and purity is presented. Variation in tether length/functionality and substitution pattern of the phenol precursors, as well as mild deprotection conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa37765070d233783f49b9f5cf51fb75
https://doi.org/10.1016/s0040-4039(98)00586-3
https://doi.org/10.1016/s0040-4039(98)00586-3
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:763-766
7-(Hydroxyimino)cyclopropa[b]chromen-la-carboxylates (4a-c), highly potent antagonists for a phospholipase C-linked metabotropic glutamate receptor, mGluR1, were synthesized through cyclopropanation onto 4-oxo-4H-1-benzopyran-2-carboxylates (5a-c) ut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acc99ca946b17668e775b43986e26c47
https://doi.org/10.1016/0960-894x(96)00104-7
https://doi.org/10.1016/0960-894x(96)00104-7
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5744753e7b7599da94e39c301acd66ae
https://doi.org/10.1002/chin.199635136
https://doi.org/10.1002/chin.199635136
Autor:
Atsuko Fukunaga, Atsuko Miyajima, Kyoko Nakanishi, Yoshiko Tamura-Horikawa, Shigeki Tamura, Mayumi Uesugi, Hirokazu Annoura
Publikováno v:
ChemInform. 31
A series of novel arylpiperidines (4a-d) which have highly potent blocking effects for both neuronal Na+ and T-type Ca2+ channels with extremely low affinity for dopamine D2 receptors were synthesized. Among these compounds, 1-(2-hydroxy-3-phenoxy)pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fd75a123446e811619b0704deb0d9e4
https://doi.org/10.1002/chin.200007120
https://doi.org/10.1002/chin.200007120
Autor:
Atsuko Fukunaga, Shigeki Tamura, Seiichi Imajo, Hirokazu Annoura, Mayumi Uesugi, Atsuko Miyajima, Kyoko Nakanishi, Yoshiko Tamura-Horikawa
Publikováno v:
ChemInform. 33
A series of novel 4-arylpiperidines and 4-aryl-4-piperidinols ( 2a – f , 3a – f and 4a – f ) was synthesized and evaluated for blocking effects on both neuronal Na + and T-type Ca 2+ channels and binding affinity for dopamine D 2 receptors. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::063d5293093f8d1cbf5dff688ac0bc76
https://doi.org/10.1002/chin.200215147
https://doi.org/10.1002/chin.200215147
Autor:
Atsuko Miyajima, Kyoko Nakanishi, Seiichi Imajo, Yoshiko Tamura-Horikawa, Hirokazu Annoura, Mayumi Uesugi, Shigeki Tamura, Atsuko Fukunaga
Publikováno v:
Bioorganicmedicinal chemistry. 10(2)
A series of novel 4-arylpiperidines and 4-aryl-4-piperidinols ( 2a – f , 3a – f and 4a – f ) was synthesized and evaluated for blocking effects on both neuronal Na + and T-type Ca 2+ channels and binding affinity for dopamine D 2 receptors. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c2d50e6d61158c50143ecbbde71a914
https://pubmed.ncbi.nlm.nih.gov/11741786
https://pubmed.ncbi.nlm.nih.gov/11741786