Kutznerides 1−4, Depsipeptides from the Actinomycete Kutzneria sp. 744 Inhabiting Mycorrhizal Roots of Picea a bies Seedlings
Bioassay-guided fractionation of culture supernatants of the actinomycete Kutzneria sp. 744 resulted in the isolation of four new depsipeptides (1−4). Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl)-d-glycine-(2S,3aR,8aS)-6,7-dichloro-3a-hydroxy-1,2,3,3a,8,8a-hexahy...
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Veröffentlicht in: | Journal of natural products (Washington, D.C.) D.C.), 2006-01, Vol.69 (1), p.97-102 |
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creator | Broberg, Anders Menkis, Audrius Vasiliauskas, Rimvydas |
description | Bioassay-guided fractionation of culture supernatants of the actinomycete Kutzneria sp. 744 resulted in the isolation of four new depsipeptides (1−4). Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl)-d-glycine-(2S,3aR,8aS)-6,7-dichloro-3a-hydroxy-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid-3-hydroxy-d-glutamic acid-O-methyl-l-serine-l-piperazic acid-(S)-2-hydroxy-3,3-dimethylbutanoic acid]. The 3-hydroxy-d-glutamic acid was present as its threo-isomer in 1 and 2 and as its erythro-isomer in 3 and 4. The piperazic acid was modified to its (R)-4-chloro analogue in 2 and to its C-5/N unsaturated analogue in 4. Compounds 1−4 displayed moderate spore germination inhibiting activity against several common root-rotting fungi. |
doi_str_mv | 10.1021/np050378g |
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Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl)-d-glycine-(2S,3aR,8aS)-6,7-dichloro-3a-hydroxy-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid-3-hydroxy-d-glutamic acid-O-methyl-l-serine-l-piperazic acid-(S)-2-hydroxy-3,3-dimethylbutanoic acid]. The 3-hydroxy-d-glutamic acid was present as its threo-isomer in 1 and 2 and as its erythro-isomer in 3 and 4. The piperazic acid was modified to its (R)-4-chloro analogue in 2 and to its C-5/N unsaturated analogue in 4. 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Nat. Prod</addtitle><description>Bioassay-guided fractionation of culture supernatants of the actinomycete Kutzneria sp. 744 resulted in the isolation of four new depsipeptides (1−4). Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl)-d-glycine-(2S,3aR,8aS)-6,7-dichloro-3a-hydroxy-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid-3-hydroxy-d-glutamic acid-O-methyl-l-serine-l-piperazic acid-(S)-2-hydroxy-3,3-dimethylbutanoic acid]. The 3-hydroxy-d-glutamic acid was present as its threo-isomer in 1 and 2 and as its erythro-isomer in 3 and 4. The piperazic acid was modified to its (R)-4-chloro analogue in 2 and to its C-5/N unsaturated analogue in 4. 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Nat. Prod</addtitle><date>2006-01-27</date><risdate>2006</risdate><volume>69</volume><issue>1</issue><spage>97</spage><epage>102</epage><pages>97-102</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Bioassay-guided fractionation of culture supernatants of the actinomycete Kutzneria sp. 744 resulted in the isolation of four new depsipeptides (1−4). Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl)-d-glycine-(2S,3aR,8aS)-6,7-dichloro-3a-hydroxy-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole-2-carboxylic acid-3-hydroxy-d-glutamic acid-O-methyl-l-serine-l-piperazic acid-(S)-2-hydroxy-3,3-dimethylbutanoic acid]. The 3-hydroxy-d-glutamic acid was present as its threo-isomer in 1 and 2 and as its erythro-isomer in 3 and 4. The piperazic acid was modified to its (R)-4-chloro analogue in 2 and to its C-5/N unsaturated analogue in 4. Compounds 1−4 displayed moderate spore germination inhibiting activity against several common root-rotting fungi.</abstract><pub>American Chemical Society</pub><doi>10.1021/np050378g</doi><tpages>6</tpages></addata></record> |
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title | Kutznerides 1−4, Depsipeptides from the Actinomycete Kutzneria sp. 744 Inhabiting Mycorrhizal Roots of Picea a bies Seedlings |
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