Matsuda A - Search Results

1

New neplanocin analogues. 7. Synthesis and antiviral activity of 2-halo derivatives of neplanocin A.

Obara T, Shuto S, Saito Y, Snoeck R, Andrei G, Balzarini J, De Clercq E, Matsuda A. Obara T, et al. Among authors: matsuda a. J Med Chem. 1996 Sep 13;39(19):3847-52. doi: 10.1021/jm960145+. J Med Chem. 1996. PMID: 8809173

2

New neplanocin analogues. 6. Synthesis and potent antiviral activity of 6'-homoneplanocin A1.

Shuto S, Obara T, Saito Y, Andrei G, Snoeck R, De Clercq E, Matsuda A. Shuto S, et al. Among authors: matsuda a. J Med Chem. 1996 Jun 7;39(12):2392-9. doi: 10.1021/jm950853f. J Med Chem. 1996. PMID: 8691433

3

New neplanocin analogues. IX. A practical preparation of (6'R)-6'-C-methylneplanocin A (RMNPA), a potent antiviral agent, and the determination of its 6'-configuration. Diastereoselective deamination by adenosine deaminase.

Shuto S, Obara T, Yaginuma S, Matsuda A. Shuto S, et al. Among authors: matsuda a. Chem Pharm Bull (Tokyo). 1997 Jan;45(1):138-42. doi: 10.1248/cpb.45.138. Chem Pharm Bull (Tokyo). 1997. PMID: 9023976

4

New neplanocin analogues. VIII. Synthesis and biological activity of 6'-C-ethyl, -ethenyl, and -ethynyl derivatives of neplanocin A.

Shuto S, Obara T, Saito Y, Yamashita K, Tanaka M, Sasaki T, Andrei G, Snoeck R, Neyts J, Padalko E, Balzarini J, De Clercq E, Matsuda A. Shuto S, et al. Among authors: matsuda a. Chem Pharm Bull (Tokyo). 1997 Jul;45(7):1163-8. doi: 10.1248/cpb.45.1163. Chem Pharm Bull (Tokyo). 1997. PMID: 9246750

5

New neplanocin analogues. 12. Alternative synthesis and antimalarial effect of (6'R)-6'-C-methylneplanocin A, a potent AdoHcy hydrolase inhibitor.

Shuto S, Minakawa N, Niizuma S, Kim HS, Wataya Y, Matsuda A. Shuto S, et al. Among authors: matsuda a. J Med Chem. 2002 Jan 31;45(3):748-51. doi: 10.1021/jm010374i. J Med Chem. 2002. PMID: 11806727

6

Synthesis of the cyclic and acyclic acetal derivatives of 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine, a potent antitumor nucleoside. Design of prodrugs to be selectively activated in tumor tissues via the bio-reduction-hydrolysis mechanism.

Nomura M, Shuto S, Matsuda A. Nomura M, et al. Among authors: matsuda a. Bioorg Med Chem. 2003 May 29;11(11):2453-61. doi: 10.1016/s0968-0896(03)00104-4. Bioorg Med Chem. 2003. PMID: 12735992

7

A method for designing conformationally restricted analogues based on allylic strain: synthesis of a novel class of noncompetitive NMDA receptor antagonists having the acrylamide structure.

Ohmori Y, Yamashita A, Tsujita R, Yamamoto T, Taniuchi K, Matsuda A, Shuto S. Ohmori Y, et al. Among authors: matsuda a. J Med Chem. 2003 Dec 4;46(25):5326-33. doi: 10.1021/jm030226n. J Med Chem. 2003. PMID: 14640541

8

Chemistry of cyclic ADP-ribose and its analogs.

Shuto S, Matsuda A. Shuto S, et al. Among authors: matsuda a. Curr Med Chem. 2004 Apr;11(7):827-45. doi: 10.2174/0929867043455639. Curr Med Chem. 2004. PMID: 15078168 Review.

9

Nucleosides and nucleotides--CXXXVII. Antitumor phospholipids with 5-fluorouridine as a cytotoxic polar-head: synthesis of 5'-phosphatidyl-5-fluorouridines by phospholipase D-catalyzed transphosphatidylation.

Shuto S, Itoh H, Sakai A, Nakagami K, Imamura S, Matsuda A. Shuto S, et al. Among authors: matsuda a. Bioorg Med Chem. 1995 Mar;3(3):235-43. doi: 10.1016/0968-0896(95)00003-y. Bioorg Med Chem. 1995. PMID: 7606385

10

(+/-)-(Z)-2-(aminomethyl)-1-phenylcyclopropanecarboxamide derivatives as a new prototype of NMDA receptor antagonists.

Shuto S, Takada H, Mochizuki D, Tsujita R, Hase Y, Ono S, Shibuya N, Matsuda A. Shuto S, et al. Among authors: matsuda a. J Med Chem. 1995 Jul 21;38(15):2964-8. doi: 10.1021/jm00015a019. J Med Chem. 1995. PMID: 7636857

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