Fuse E - Search Results

1

Novel and orally active 5-(1,3,4-oxadiazol-2-yl)pyrimidine derivatives as selective FLT3 inhibitors.

Ishida H, Isami S, Matsumura T, Umehara H, Yamashita Y, Kajita J, Fuse E, Kiyoi H, Naoe T, Akinaga S, Shiotsu Y, Arai H. Ishida H, et al. Among authors: fuse e. Bioorg Med Chem Lett. 2008 Oct 15;18(20):5472-7. doi: 10.1016/j.bmcl.2008.09.031. Epub 2008 Sep 11. Bioorg Med Chem Lett. 2008. PMID: 18835166

2

Design and synthesis of potent antitumor 5,4'-diaminoflavone derivatives based on metabolic considerations.

Akama T, Ishida H, Shida Y, Kimura U, Gomi K, Saito H, Fuse E, Kobayashi S, Yoda N, Kasai M. Akama T, et al. Among authors: fuse e. J Med Chem. 1997 Jun 6;40(12):1894-900. doi: 10.1021/jm9700326. J Med Chem. 1997. PMID: 9191967

3

Synthetic study of VLA-4/VCAM-1 inhibitors: synthesis and structure-activity relationship of piperazinylphenylalanine derivatives.

Saku O, Ohta K, Arai E, Nomoto Y, Miura H, Nakamura H, Fuse E, Nakasato Y. Saku O, et al. Among authors: fuse e. Bioorg Med Chem Lett. 2008 Feb 1;18(3):1053-7. doi: 10.1016/j.bmcl.2007.12.014. Epub 2007 Dec 14. Bioorg Med Chem Lett. 2008. PMID: 18160288

4

Effects of olopatadine, a new antiallergic agent, on human liver microsomal cytochrome P450 activities.

Kajita J, Inano K, Fuse E, Kuwabara T, Kobayashi H. Kajita J, et al. Among authors: fuse e. Drug Metab Dispos. 2002 Dec;30(12):1504-11. doi: 10.1124/dmd.30.12.1504. Drug Metab Dispos. 2002. PMID: 12433826

5

The contribution of cytochrome P450 to the metabolism of tegafur in human liver.

Kajita J, Fuse E, Kuwabara T, Kobayashi H. Kajita J, et al. Among authors: fuse e. Drug Metab Pharmacokinet. 2003;18(5):303-9. doi: 10.2133/dmpk.18.303. Drug Metab Pharmacokinet. 2003. PMID: 15618749 Free article.

6

Pharmacokinetics and pharmacodynamics of a novel protein kinase inhibitor, UCN-01.

Kurata N, Kuwabara T, Tanii H, Fuse E, Akiyama T, Akinaga S, Kobayashi H, Yamaguchi K, Kobayashi S. Kurata N, et al. Among authors: fuse e. Cancer Chemother Pharmacol. 1999;44(1):12-8. doi: 10.1007/s002800050939. Cancer Chemother Pharmacol. 1999. PMID: 10367744

7

Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance.

Suzuki F, Shimada J, Shiozaki S, Ichikawa S, Ishii A, Nakamura J, Nonaka H, Kobayashi H, Fuse E. Suzuki F, et al. Among authors: fuse e. J Med Chem. 1993 Aug 20;36(17):2508-18. doi: 10.1021/jm00069a009. J Med Chem. 1993. PMID: 8355252

8

Unpredicted clinical pharmacology of UCN-01 caused by specific binding to human alpha1-acid glycoprotein.

Fuse E, Tanii H, Kurata N, Kobayashi H, Shimada Y, Tamura T, Sasaki Y, Tanigawara Y, Lush RD, Headlee D, Figg WD, Arbuck SG, Senderowicz AM, Sausville EA, Akinaga S, Kuwabara T, Kobayashi S. Fuse E, et al. Cancer Res. 1998 Aug 1;58(15):3248-53. Cancer Res. 1998. PMID: 9699650 Clinical Trial.

9

Inhibitory effect of the 4-aminotetrahydroquinoline derivatives, selective chemoattractant receptor-homologous molecule expressed on T helper 2 cell antagonists, on eosinophil migration induced by prostaglandin D2.

Mimura H, Ikemura T, Kotera O, Sawada M, Tashiro S, Fuse E, Ueno K, Manabe H, Ohshima E, Karasawa A, Miyaji H. Mimura H, et al. Among authors: fuse e. J Pharmacol Exp Ther. 2005 Jul;314(1):244-51. doi: 10.1124/jpet.104.081539. Epub 2005 Mar 29. J Pharmacol Exp Ther. 2005. PMID: 15798001

10

P-glycoprotein limits the brain penetration of olopatadine hydrochloride, H1-receptor antagonist.

Mimura N, Nagata Y, Kuwabara T, Kubo N, Fuse E. Mimura N, et al. Among authors: fuse e. Drug Metab Pharmacokinet. 2008;23(2):106-14. doi: 10.2133/dmpk.23.106. Drug Metab Pharmacokinet. 2008. PMID: 18445990 Free article.

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