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Volumn 26, Issue 6-7, 2007, Pages 729-732

Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase

Author keywords

Homo apione planocin A; Ring closing metathesis; S adenosylhomocysteine hydrolase

Indexed keywords

ADENOSYLHOMOCYSTEINASE INHIBITOR; HOMO APIONEPLANOCIN A; UNCLASSIFIED DRUG;

EID: 36949001351     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770701493559     Document Type: Conference Paper
Times cited : (1)

References (8)
  • 1
    • 0019468688 scopus 로고
    • Studies on neplanocin A, new antitumor antibiotic. I. Producing organism, isolation and characterization
    • Yaginuma, S.; Muto, N.; Tsujino, M.; Sudate, Y.; Hayashi, M.; Otani, M. Studies on neplanocin A, new antitumor antibiotic. I. Producing organism, isolation and characterization. J. Antibiot. 1981, 34, 359-366.
    • (1981) J. Antibiot , vol.34 , pp. 359-366
    • Yaginuma, S.1    Muto, N.2    Tsujino, M.3    Sudate, Y.4    Hayashi, M.5    Otani, M.6
  • 3
    • 0021227696 scopus 로고
    • A potent Inhibitor of S-adenosylhomocysteine hydrolase and of vaccinia virus multiplication in mouse L929 cells
    • Borchardt, R.T.; Keller, B.T.; Patel-Thombre, U. Neplanocin A. A potent Inhibitor of S-adenosylhomocysteine hydrolase and of vaccinia virus multiplication in mouse L929 cells. J. Biol. Chem. 1984, 259, 4353-4358.
    • (1984) J. Biol. Chem , vol.259 , pp. 4353-4358
    • Borchardt, R.T.1    Keller, B.T.2    Patel-Thombre, U.3    Neplanocin, A.4
  • 4
    • 0026571540 scopus 로고
    • New Neplanocin Analogs. 1. Synthesis of 6′-modified neplanocin A derivatives as broad-spectrum antiviral agents
    • Shuto, S.; Obara, T.; Toriya, M.; Hosoya, M.; Snoeck, R.; Andrei, G.; Balzarini, J.; De Clercq, E. New Neplanocin Analogs. 1. Synthesis of 6′-modified neplanocin A derivatives as broad-spectrum antiviral agents. J. Med. Chem. 1992, 35, 324-331.
    • (1992) J. Med. Chem , vol.35 , pp. 324-331
    • Shuto, S.1    Obara, T.2    Toriya, M.3    Hosoya, M.4    Snoeck, R.5    Andrei, G.6    Balzarini, J.7    De Clercq, E.8
  • 5
    • 0025909708 scopus 로고
    • Synthesis of chiral 3-substituted gamma-lactones and 9-furanosyladenine from (R)-2-(2,2-diethoxyethyl)-1,3- propanediol monoacetate prepared by lipase-catalyzed reaction
    • Terao, Y.; Akamatsu, M.; Achiwa, K. Synthesis of chiral 3-substituted gamma-lactones and 9-furanosyladenine from (R)-2-(2,2-diethoxyethyl)-1,3- propanediol monoacetate prepared by lipase-catalyzed reaction. Chem. Pharm. Bull. 1991, 39, 823-825.
    • (1991) Chem. Pharm. Bull , vol.39 , pp. 823-825
    • Terao, Y.1    Akamatsu, M.2    Achiwa, K.3
  • 6
    • 0037015428 scopus 로고    scopus 로고
    • Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase iinhibitor
    • Moon, H.R.; Kim, H.O.; Lee, K.M.; Chun, M.W.; Kim, J.H.; Jeong, L.S. Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase iinhibitor. Org. Lett. 2002, 4, 3501-3503.
    • (2002) Org. Lett , vol.4 , pp. 3501-3503
    • Moon, H.R.1    Kim, H.O.2    Lee, K.M.3    Chun, M.W.4    Kim, J.H.5    Jeong, L.S.6
  • 7
    • 0029894001 scopus 로고    scopus 로고
    • New neplanocin analogues. 6. Synthesis and potent antiviral acitivity of 6′-homoneplanocin A
    • Shuto, S.; Obara, T.; Saito, Y.; Andrei, G.; Snoeck, R.; De Clercq, E.; Matsuda, A. New neplanocin analogues. 6. Synthesis and potent antiviral acitivity of 6′-homoneplanocin A. J. Med. Chem. 1996, 39, 2392-2399.
    • (1996) J. Med. Chem , vol.39 , pp. 2392-2399
    • Shuto, S.1    Obara, T.2    Saito, Y.3    Andrei, G.4    Snoeck, R.5    De Clercq, E.6    Matsuda, A.7
  • 8
    • 0034596301 scopus 로고    scopus 로고
    • The stereoselective synthesis of 4′-β-thioribonucleosides via the Pummerer reaction
    • Naka, T.; Minakawa, N.; Abe, H.; Kaga, D.; Matsuda, A. The stereoselective synthesis of 4′-β-thioribonucleosides via the Pummerer reaction. J. Am. Chem. Soc. 2000, 122, 7233-7243.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 7233-7243
    • Naka, T.1    Minakawa, N.2    Abe, H.3    Kaga, D.4    Matsuda, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.