Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Teruo Shiomi"'
Publikováno v:
Brain Research. 577:57-63
Ischemia for 5 min temporarily increased locomotor activity in gerbils after 1 and 3 days. Temporary increases were also noted within 7 and 5 days after 20-min ischemia and repeated ischemia (three 2-min ischemia at 1-h intervals), respectively. In a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23204bcf946c350304e55d5049a6ba2
https://doi.org/10.1016/0006-8993(92)90537-j
https://doi.org/10.1016/0006-8993(92)90537-j
Autor:
Masami Eigyo, Teruo Shiomi, Yuzuru Inoue, Isako Sakaguchi, Chiyomi Ishibashi, Shunji Murata, Kiyotaka Koyabu, Akira Matsushita, Ikuo Adachi, Motohiko Ueda
Publikováno v:
Japanese journal of pharmacology. 65(2)
S-312, S-312-d, but not S-312-l, L-type calcium channel antagonists, showed anticonvulsant effects on the audiogenic tonic convulsions in DBA/2 mice; and their ED50 values were 18.4 (12.8-27.1) mg/kg, p.o. and 15.0 (10.2-23.7) mg/kg, p.o., respective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93de976f90a18651cf2253fe0171c86e
https://pubmed.ncbi.nlm.nih.gov/7967231
https://pubmed.ncbi.nlm.nih.gov/7967231
Publikováno v:
Japanese Journal of Pharmacology. 73:211
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaf44384a3daf9b768ba2f8c81d64ff0
https://doi.org/10.1016/s0021-5198(19)45346-8
https://doi.org/10.1016/s0021-5198(19)45346-8
Autor:
Teruo Shiomi, Kohji Yoshimura, Haruyuki Shintaku, Isako Sakaguchi, Chiyomi Ishibashi, Masahito Horiuchi, Yukio Takahara, Goro Katsuura
Publikováno v:
Japanese Journal of Pharmacology. 71:239
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74ffed66374daa95f084ed77095d4da8
https://doi.org/10.1016/s0021-5198(19)37195-1
https://doi.org/10.1016/s0021-5198(19)37195-1
Publikováno v:
Japanese Journal of Pharmacology. 55:355
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90166506bcd6177c00dd0796e79e2d88
https://doi.org/10.1016/s0021-5198(19)39451-x
https://doi.org/10.1016/s0021-5198(19)39451-x
Autor:
Teruo Shiomi, Yoshikazu Matsuo, Masami Eigyo, Yasuhiro Nishibe, Katsumi Hirose, Toshio Yoshizaki
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 321:190-194
Sulpiride (SUL) is more efficacious in antipsychotic activity than metoclopramide (MET), although both appear to possess almost equal affinities for dopamine (DA) receptors. We studied the effects of SUL and MET on the brain homovanillic acid (HVA) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d759feee11d31560df72c1d7698ebfb
https://doi.org/10.1007/bf00505484
https://doi.org/10.1007/bf00505484
Autor:
Akira Matsushita, Haruyuki Shintaku, Tsutomu Sugasawa, Kazuyuki Sasakura, Makoto Adachi, Teruo Shiomi, Shunji Murata, Masami Eigyo, Yukio Takahara
Publikováno v:
Journal of Medicinal Chemistry. 28:699-707
A series of 1-azacycloalkyl-1,4-benzodiazepin-2-ones were synthesized from 1-azacycloalkyl-2-benzoylanilines and corresponding imines and then evaluated for their central nervous system activities. Pharmacological data showed that some of these compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::372d719b52ddec3afe78889f2fef146b
https://doi.org/10.1021/jm00383a003
https://doi.org/10.1021/jm00383a003
Publikováno v:
THE JOURNAL OF VITAMINOLOGY. 12:49-58
Large amounts of ascorbic acid are recently used in curing pigment anomalies. Investigation was therefore carried out in animals and man on the fate of the vitamin administered in large amounts, especially on the excretion of oxalic acid and the foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40757b056668a19dbd143d2c427574f2
https://doi.org/10.5925/jnsv1954.12.49
https://doi.org/10.5925/jnsv1954.12.49
Publikováno v:
Journal of medicinal chemistry. 27(9)
A series of some novel N-[(1-ethyl-2-pyrrolidinyl)methyl]benzamides involving replacement of the sulfamoyl group in sulpiride with a sulfonamido group was synthesized and tested for dopamine receptor blockade. In comparison with sulpiride, several co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90412584dfb875e44214e8e7649a191
https://pubmed.ncbi.nlm.nih.gov/6147414
https://pubmed.ncbi.nlm.nih.gov/6147414
Publikováno v:
Chemischer Informationsdienst. 16
A series of some novel N-[(1-ethyl-2-pyrrolidinyl)methyl]benzamides involving replacement of the sulfamoyl group in sulpiride with a sulfonamido group was synthesized and tested for dopamine receptor blockade. In comparison with sulpiride, several co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81b73d2fd177a5946b8edec3145ee1e3
https://doi.org/10.1002/chin.198505209
https://doi.org/10.1002/chin.198505209