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Anti-inflammatory, analgesic, and antipyretic effects and gastrointestinal toxicity of the new anti-inflammatory drug N-(3-[3-(piperidinylmethyl)phenoxy]propyl)-carbamoylmethylthio ]ethyl 1-(p-chlorobenzoyl) 5-methoxy-2-methyl-3-indolylacetate.
Arzneimittelforschung. 1992 Jul;42(7):954-8.
Arzneimittelforschung. 1992.
PMID: 1418061
These results suggest the clinical applicability of this drug in the long-term therapy of inflammatory diseases such as rheumatoid arthritis....
These results suggest the clinical applicability of this drug in the long-term therapy of inflammatory diseases such as rheumatoid ar …
[The gastric mucosal adhesiveness of Z-103 in rats with chronic ulcer].
Seiki M, Aita H, Mera Y, Arai K, Toyama S, Furuta S, Morita H, Hori Y, Yoneta T, Tagashira E.
Seiki M, et al. Among authors: tagashira e.
Nihon Yakurigaku Zasshi. 1992 Apr;99(4):255-63. doi: 10.1254/fpj.99.255.
Nihon Yakurigaku Zasshi. 1992.
PMID: 1607133
Japanese.
On the other hand, although ZnSO4 and ZnSO4+carnosine combination macroscopically produced generally the same level of adhesiveness as Z-103, when the gastric tissue Zn content for Z-103 and ZnSO4 were compared, the Zn content of ZnSO4 was lower than that for Z-103 at both the no …
On the other hand, although ZnSO4 and ZnSO4+carnosine combination macroscopically produced generally the same level of adhesiveness as Z-103 …
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Biochemical aspects of experimental barbital dependence II: Effect on glycometabolism.
Yanaura S, Kakuno K, Nakao K, Tagashira E.
Yanaura S, et al. Among authors: tagashira e.
Jpn J Pharmacol. 1983 Apr;33(2):395-402. doi: 10.1254/jjp.33.395.
Jpn J Pharmacol. 1983.
PMID: 6684191
Free article.
Barbital depresses the central glycometabolism, and at the dependent stage (long term barbital dosing, 36 days or more), metabolism was almost same as the control. ...
Barbital depresses the central glycometabolism, and at the dependent stage (long term barbital dosing, 36 days or more), metabolism w …
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Tolerance to and dependence on barbiturates in mice reference to the data in rats.
Tagashira E, Urano T, Yasukouchi K, Hiramori T, Yanaura S.
Tagashira E, et al.
Jpn J Pharmacol. 1981 Jun;31(3):375-82. doi: 10.1254/jjp.31.375.
Jpn J Pharmacol. 1981.
PMID: 7198164
Free article.
Contrary to the findings in rats, in which there was a frequent incidence of convulsion from 17 to 48 hours after withdrawal, the duration of the characteristic signs after barbiturate withdrawal was obviously short-term. These results suggest that may be more reasonable t …
Contrary to the findings in rats, in which there was a frequent incidence of convulsion from 17 to 48 hours after withdrawal, the duration o …
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