Endo N - Search Results

1

Rifampicin inhibits the toxicity of pre-aggregated amyloid peptides by binding to peptide fibrils and preventing amyloid-cell interaction.

Tomiyama T, Kaneko H, Kataoka Ki, Asano S, Endo N. Tomiyama T, et al. Among authors: endo n. Biochem J. 1997 Mar 15;322 ( Pt 3)(Pt 3):859-65. doi: 10.1042/bj3220859. Biochem J. 1997. PMID: 9148761 Free PMC article.

2

Rifampicin prevents the aggregation and neurotoxicity of amyloid beta protein in vitro.

Tomiyama T, Asano S, Suwa Y, Morita T, Kataoka K, Mori H, Endo N. Tomiyama T, et al. Among authors: endo n. Biochem Biophys Res Commun. 1994 Oct 14;204(1):76-83. doi: 10.1006/bbrc.1994.2428. Biochem Biophys Res Commun. 1994. PMID: 7945395

3

Inhibition of amyloid beta protein aggregation and neurotoxicity by rifampicin. Its possible function as a hydroxyl radical scavenger.

Tomiyama T, Shoji A, Kataoka K, Suwa Y, Asano S, Kaneko H, Endo N. Tomiyama T, et al. Among authors: endo n. J Biol Chem. 1996 Mar 22;271(12):6839-44. doi: 10.1074/jbc.271.12.6839. J Biol Chem. 1996. PMID: 8636108 Free article.

4

Racemization of Asp23 residue affects the aggregation properties of Alzheimer amyloid beta protein analogues.

Tomiyama T, Asano S, Furiya Y, Shirasawa T, Endo N, Mori H. Tomiyama T, et al. Among authors: endo n. J Biol Chem. 1994 Apr 8;269(14):10205-8. J Biol Chem. 1994. PMID: 8144598 Free article.

5

Racemization: its biological significance on neuropathogenesis of Alzheimer's disease.

Mori H, Ishii K, Tomiyama T, Furiya Y, Sahara N, Asano S, Endo N, Shirasawa T, Takio K. Mori H, et al. Among authors: endo n. Tohoku J Exp Med. 1994 Nov;174(3):251-62. doi: 10.1620/tjem.174.251. Tohoku J Exp Med. 1994. PMID: 7761990 Free article.

6

Small molecule inhibitors of the CCR2b receptor. Part 1: Discovery and optimization of homopiperazine derivatives.

Imai M, Shiota T, Kataoka K, Tarby CM, Moree WJ, Tsutsumi T, Sudo M, Ramirez-Weinhouse MM, Comer D, Sun CM, Yamagami S, Tanaka H, Morita T, Hada T, Greene J, Barnum D, Saunders J, Myers PL, Kato Y, Endo N. Imai M, et al. Among authors: endo n. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5407-11. doi: 10.1016/j.bmcl.2004.08.008. Bioorg Med Chem Lett. 2004. PMID: 15454235

7

Potent antagonists of the CCR2b receptor. Part 3: SAR of the (R)-3-aminopyrrolidine series.

Moree WJ, Kataoka K, Ramirez-Weinhouse MM, Shiota T, Imai M, Tsutsumi T, Sudo M, Endo N, Muroga Y, Hada T, Fanning D, Saunders J, Kato Y, Myers PL, Tarby CM. Moree WJ, et al. Among authors: endo n. Bioorg Med Chem Lett. 2008 Mar 15;18(6):1869-73. doi: 10.1016/j.bmcl.2008.02.015. Epub 2008 Feb 10. Bioorg Med Chem Lett. 2008. PMID: 18313297

8

Full active baculovirus-expressed human monocyte chemoattractant protein 1 with the intact N-terminus.

Ishii K, Yamagami S, Tanaka H, Motoki M, Suwa Y, Endo N. Ishii K, et al. Among authors: endo n. Biochem Biophys Res Commun. 1995 Jan 26;206(3):955-61. doi: 10.1006/bbrc.1995.1135. Biochem Biophys Res Commun. 1995. PMID: 7832810

9

cDNA cloning and functional expression of a human monocyte chemoattractant protein 1 receptor.

Yamagami S, Tokuda Y, Ishii K, Tanaka H, Endo N. Yamagami S, et al. Among authors: endo n. Biochem Biophys Res Commun. 1994 Jul 29;202(2):1156-62. doi: 10.1006/bbrc.1994.2049. Biochem Biophys Res Commun. 1994. PMID: 8048929

10

Small molecule antagonists of the CCR2b receptor. Part 2: Discovery process and initial structure-activity relationships of diamine derivatives.

Moree WJ, Kataoka K, Ramirez-Weinhouse MM, Shiota T, Imai M, Sudo M, Tsutsumi T, Endo N, Muroga Y, Hada T, Tanaka H, Morita T, Greene J, Barnum D, Saunders J, Kato Y, Myers PL, Tarby CM. Moree WJ, et al. Among authors: endo n. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5413-6. doi: 10.1016/j.bmcl.2004.08.009. Bioorg Med Chem Lett. 2004. PMID: 15454236

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