Kinoshita T - Search Results

1

Structural insights for producing CK2α1-specific inhibitors.

Tsuyuguchi M, Nakaniwa T, Hirasawa A, Nakanishi I, Kinoshita T. Tsuyuguchi M, et al. Among authors: kinoshita t. Bioorg Med Chem Lett. 2020 Jan 15;30(2):126837. doi: 10.1016/j.bmcl.2019.126837. Epub 2019 Dec 3. Bioorg Med Chem Lett. 2020. PMID: 31859160

2

True interaction mode of porcine pancreatic elastase with FR136706, a potent peptidyl inhibitor.

Kinoshita T, Nakanishi I, Sato A, Tada T. Kinoshita T, et al. Bioorg Med Chem Lett. 2003 Jan 6;13(1):21-4. doi: 10.1016/s0960-894x(02)00852-1. Bioorg Med Chem Lett. 2003. PMID: 12467609

3

Structure of bovine adenosine deaminase complexed with 6-hydroxy-1,6-dihydropurine riboside.

Kinoshita T, Nishio N, Nakanishi I, Sato A, Fujii T. Kinoshita T, et al. Acta Crystallogr D Biol Crystallogr. 2003 Feb;59(Pt 2):299-303. doi: 10.1107/s090744490202190x. Epub 2003 Jan 23. Acta Crystallogr D Biol Crystallogr. 2003. PMID: 12554940

4

Structure-based de novo design of non-nucleoside adenosine deaminase inhibitors.

Terasaka T, Nakanishi I, Nakamura K, Eikyu Y, Kinoshita T, Nishio N, Sato A, Kuno M, Seki N, Sakane K. Terasaka T, et al. Among authors: kinoshita t. Bioorg Med Chem Lett. 2003 Mar 24;13(6):1115-8. doi: 10.1016/s0960-894x(03)00026-x. Bioorg Med Chem Lett. 2003. PMID: 12643924

5

Inhibitor-induced structural change of the active site of human poly(ADP-ribose) polymerase.

Kinoshita T, Nakanishi I, Warizaya M, Iwashita A, Kido Y, Hattori K, Fujii T. Kinoshita T, et al. FEBS Lett. 2004 Jan 2;556(1-3):43-6. doi: 10.1016/s0014-5793(03)01362-0. FEBS Lett. 2004. PMID: 14706823 Free article.

6

A highly potent non-nucleoside adenosine deaminase inhibitor: efficient drug discovery by intentional lead hybridization.

Terasaka T, Kinoshita T, Kuno M, Nakanishi I. Terasaka T, et al. Among authors: kinoshita t. J Am Chem Soc. 2004 Jan 14;126(1):34-5. doi: 10.1021/ja038606l. J Am Chem Soc. 2004. PMID: 14709046

7

Structure-based design and synthesis of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors.

Terasaka T, Okumura H, Tsuji K, Kato T, Nakanishi I, Kinoshita T, Kato Y, Kuno M, Seki N, Naoe Y, Inoue T, Tanaka K, Nakamura K. Terasaka T, et al. Among authors: kinoshita t. J Med Chem. 2004 May 20;47(11):2728-31. doi: 10.1021/jm0499559. J Med Chem. 2004. PMID: 15139750

8

Structure-based design, synthesis, and structure-activity relationship studies of novel non-nucleoside adenosine deaminase inhibitors.

Terasaka T, Kinoshita T, Kuno M, Seki N, Tanaka K, Nakanishi I. Terasaka T, et al. Among authors: kinoshita t. J Med Chem. 2004 Jul 15;47(15):3730-43. doi: 10.1021/jm0306374. J Med Chem. 2004. PMID: 15239652

9

Rational design of non-nucleoside, potent, and orally bioavailable adenosine deaminase inhibitors: predicting enzyme conformational change and metabolism.

Terasaka T, Tsuji K, Kato T, Nakanishi I, Kinoshita T, Kato Y, Kuno M, Inoue T, Tanaka K, Nakamura K. Terasaka T, et al. Among authors: kinoshita t. J Med Chem. 2005 Jul 28;48(15):4750-3. doi: 10.1021/jm050413g. J Med Chem. 2005. PMID: 16033254

10

Structural basis of compound recognition by adenosine deaminase.

Kinoshita T, Nakanishi I, Terasaka T, Kuno M, Seki N, Warizaya M, Matsumura H, Inoue T, Takano K, Adachi H, Mori Y, Fujii T. Kinoshita T, et al. Biochemistry. 2005 Aug 9;44(31):10562-9. doi: 10.1021/bi050529e. Biochemistry. 2005. PMID: 16060665

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,545 results

Search Page

Filters