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新型Hydantocidin类似物的研究进展 被引量:9

Progress on the Synthesis of Novel Hydantocidin Analogues
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摘要 Hydantocidin是一个天然螺核苷类化合物,具有较高的内吸性除草活性,但对非靶标生物毒性低,极具开发潜力。近年来,人们对Hydantocidin的糖类、脱氧类似物、环二肽、交联结构类似物等新型衍生物的合成及生物活性进行了研究,并取得了丰富的研究成果。对这些新型Hydantocidin类似物的研究进展进行了综述。 Hydantocidin is the first natural spiro-nucleoside which was isolated from the culture broth of Streptomyces hygroscopicus SANK 63584. It exhibited potential herbicidal activity with efficiency similar to glyphosate against lots of weeds with high selective toxicity between plants and animals. Recently, the novel hydantocidin analogues including carbohydrate, deoxy, cyclopeptide, and hybrid analogues were synthesized and their activity was assayed. The progress on the research of these novel hydantocidin analogues was reviewed.
出处 《农药学学报》 CAS CSCD 2008年第4期392-403,共12页 Chinese Journal of Pesticide Science
基金 国家自然科学基金资助项目(No.20772150) "863"计划资助项目(No.2006AA10A209)
关键词 Hydantocidin 类似物 合成 生物活性 hydantocidin analogue synthesis biological activity
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参考文献28

  • 1NAKAJIMA M, ITOI K, TAKAMATSU K, et al. Hydantocidin: a New Compound with Herbicidal Activity from Streptomyces hygroscopicus[J]. J Antibiot , 1991,44:293-300.
  • 2HARUYAMA H, TAKAYAMA T, KINOSHITA T, et al. Structural Elucidation and Solution Conformation of the Novel Herbicide Hydantocidin[J]. J Chem Soc. Perkin Trans I , 1991 : 1637-1640.
  • 3AGS1MUNDIN Y S, MUMPER M W, HOSMANE R S. Inhibitors of Glycogen Phosphorylase b : Synthesis, Biochemical Screening, and Molecular Modeling Studies of Novel Analogs of Hydantocidin [ J]. Bioorg Med Chem, 1998,6:911-923.
  • 4OSZ E, SO'S E, SOMSA'K L, et al. A Straightforward Route to Hydantocidin Analogs with Pyranose Ring Structure [ J]. Tetrahedron, 1997,53:5813-5824.
  • 5OSZ E,SOMS'K L,SZILA'GYI L,et al. Efficient Inhibition of Muscle and Liver Glycogen Phosphorylases by a New Glucopyranosylidene-Spirothiohydantoin[J]. Bioorg Med Chem Lett, 1999,9 : 1385-1390.
  • 6BRANDSTETTER T W, WORMALD M R, DWEK R A, et al. A Galactopyranose Analog of Hydantocidin [ J ]. Tetrahedron: Asymmetry, 1996,7 : 157-170.
  • 7BICHAND C J F, MITCHELL E P, WORMALD M R, et al. Potent Inhibition of Glycogen Phosphorylase by a Spirohydantoin of Glucopyranose: First Pyranose Analogs of Hydantocidin[J]. Tetrahedron Lett, 1995,36:2145-2148.
  • 8DE LA FUENTE C, KRULLE T M, WATSON K A,et al. Glucopyranose Spirohydantoins. Specific Inhibitors of Glycogen Phosphorylase [ J]. Synlett, 1997:485-487.
  • 9ESTEVEZ J C, SMITH M D, WORMALD M R, et al. Mimics of L-Rhanmose: Analogs of Rhamnopymnose Containing a Constituent-Amino Acid at the Anomeric Position. a Rhamnopyranose Analog of Hydantocidin [ J ].Tetrahedron : Asymmetry, 1996,7:391-394.
  • 10BRANDSTETTER T W, KIM Y H, SON J C, et al. Spirohydantoins of Glucofuranose: Analogs of Hydantocidin [ J]. Tetrahedron Lett, 1995,36:2149-2152.

同被引文献54

  • 1杨华铮,邹小毛,王磊光,程慕如.新型除草剂H-9201的研究与开发历程[J].华中师范大学学报(自然科学版),2006,40(4):532-539. 被引量:4
  • 2MIO S, ICHINOSE R, GOTO K, et al. Synthetic Studies on ( + )-Hydantocidin. I. A Total Synthesis of Hydantocidin, a New Herbicidal Metabolite from Microorganism [ J ]. Tetrahedron, 1991,47 : 2111-2120.
  • 3MUNEHARU M, MIO S. Preparation of Spirohydantoin Compounds as Herbicides: JP 89167661 [P]. 1990-03-26.
  • 4MIO S, KUMAGANA Y, SUGAI S. Synthetic Studies on ( + ) - hydantocidin. Ⅲ A New Synthetic Method for Construction of the Spiro-hydantoin Ring at the Anomeric Position of D- Ribofuranose[ J]. Tetrahedron, 1991,47 : 2133-2144.
  • 5MATSUMOTO M, KIRIHARA M, YOSHINO T, et al. A Novel Biogenetic Type Synthesis of ( + ) -Hydantocidin [ J ]. Tetrahedron Lett, 1993,34 : 6289-6292.
  • 6NAKAJIMA N, MATSUMOTO M, KIRIHARA M, et al. Novel Synthesis of ( + )-Hydantocidin Based on the Plausible Biosynthetic Pathway[ J]. Tetrahedron, 1996,52 : 1177-1194.
  • 7NAKAJIMA N, KIRIHARA M, MATSUMOTO M, et al. One-step Synthesis of ( - ) -5 -epi-Hydantocidin [ J ]. Heterocycles, 1996,42 : 503-508.
  • 8CHEMLA P. Stereoselective Synthesis of ( + )-Hydantocidin [ J]. Tetrahedron Lett, 1993,34 : 7391-7394.
  • 9FRUEH T, CHEMLA P, EGRHER J, et al. Natural Products as Pesticides: Two Examples of Stereoselective Synthesis[ J ]. Pestic Sci, 1996,46 : 37-47.
  • 10CHEMLA P. Preparation of ( + )-Hydantocidin Derivatives as Synthons for 1,1 '-Disubstituted and 1 '-Spironucleosides : US 5641882 [ P ]. 1997-06-24.

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