Maeda M - Search Results

1

DNA-binding peptides searched from the solid-phase combinatorial library with the use of the magnetic beads attaching the target duplex DNA.

Alam MR, Maeda M, Sasaki S. Alam MR, et al. Among authors: maeda m. Bioorg Med Chem. 2000 Feb;8(2):465-73. doi: 10.1016/s0968-0896(99)00298-9. Bioorg Med Chem. 2000. PMID: 10722170

2

Design of new inhibitors for cdc2 kinase based on a multiple pseudosubstrate structure.

Sasaki S, Hashimoto T, Obana N, Yasuda H, Uehara Y, Maeda M. Sasaki S, et al. Among authors: maeda m. Bioorg Med Chem Lett. 1998 May 5;8(9):1019-22. doi: 10.1016/s0960-894x(98)00163-2. Bioorg Med Chem Lett. 1998. PMID: 9871700

3

DNA binding affinity of pentapeptides selected from combinatorial library.

Alam MR, Maeda M, Sasaki S. Alam MR, et al. Among authors: maeda m. Nucleic Acids Symp Ser. 1999;(42):173-4. doi: 10.1093/nass/42.1.173. Nucleic Acids Symp Ser. 1999. PMID: 10780435

4

Selective reaction to a flipping cytidine of the duplex DNA mediated by triple helix formation.

Nagatsugi F, Usui D, Kawasaki T, Maeda M, Sasaki S. Nagatsugi F, et al. Among authors: maeda m. Bioorg Med Chem Lett. 2001 Feb 12;11(3):343-5. doi: 10.1016/s0960-894x(00)00666-1. Bioorg Med Chem Lett. 2001. PMID: 11212106

5

A new reactive nucleoside analogue for highly reactive and selective cross-linking reaction to cytidine under neutral conditions.

Nagatsugi F, Tokuda N, Maeda M, Sasaki S. Nagatsugi F, et al. Among authors: maeda m. Bioorg Med Chem Lett. 2001 Oct 8;11(19):2577-9. doi: 10.1016/s0960-894x(01)00505-4. Bioorg Med Chem Lett. 2001. PMID: 11551753

6

Solid-Phase synthesis of a library constructed of aromatic phosphate, long alkyl chains and tryptophane components, and identification of potent dipeptide telomerase inhibitors.

Sasaki S, Ehara T, Alam MR, Fujino Y, Harada N, Kimura J, Nakamura H, Maeda M. Sasaki S, et al. Among authors: maeda m. Bioorg Med Chem Lett. 2001 Oct 8;11(19):2581-4. doi: 10.1016/s0960-894x(01)00507-8. Bioorg Med Chem Lett. 2001. PMID: 11551754

7

Molecular design of inhibitors of in vitro oriC DNA replication based on the potential to block the ATP binding of DnaA protein.

Mizushima T, Sasaki S, Ohishi H, Kobayashi M, Katayama T, Miki T, Maeda M, Sekimizu K. Mizushima T, et al. Among authors: maeda m. J Biol Chem. 1996 Oct 11;271(41):25178-83. doi: 10.1074/jbc.271.41.25178. J Biol Chem. 1996. PMID: 8810275 Free article.

We earlier reported that 3-acetoxy-2,2'-bi-1H-indol inhibited the ATP binding to DnaA protein (Sasaki, S., Mizushima, T., Hashimoto, T., Maeda, M., and Sekimizu, K. (1994) Bioorg. Med. Chem. Lett. 4, 1771-1774). In the present study, derivatives of 3-acetoxy-2,2'-bi …

We earlier reported that 3-acetoxy-2,2'-bi-1H-indol inhibited the ATP binding to DnaA protein (Sasaki, S., Mizushima, T., Hashimoto, T., …

8

Excellent acceleration of the Diels-Alder reaction by microwave irradiation for the synthesis of new fluorine-substituted ligands of NMDA receptor.

Sasaki S, Ishibashi N, Kuwamura T, Sano H, Matoba M, Nisikawa T, Maeda M. Sasaki S, et al. Among authors: maeda m. Bioorg Med Chem Lett. 1998 Nov 3;8(21):2983-6. doi: 10.1016/S0960-894X(98)00541-1. Bioorg Med Chem Lett. 1998. PMID: 9873659

9

Efficient cross-linking to cytidine by functional nucleobases capable of in situ activation.

Kawasaki T, Nagatsugi F, Usui D, Maeda M, Sasaki S. Kawasaki T, et al. Among authors: maeda m. Nucleic Acids Symp Ser. 1999;(42):43-4. doi: 10.1093/nass/42.1.43. Nucleic Acids Symp Ser. 1999. PMID: 10780370

10

Novel DNA-binding ligands with sequence selectivity based on hydrophobic structure.

Shibata T, Torigoe H, Shibata Y, Maeda M, Sasaki S. Shibata T, et al. Among authors: maeda m. Nucleic Acids Symp Ser. 1999;(42):251-2. doi: 10.1093/nass/42.1.251. Nucleic Acids Symp Ser. 1999. PMID: 10780474

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