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description
| - wetenschappelijk artikel (nl)
- наукова стаття, опублікована в лютому 1999 (uk)
- article scientifique publié en 1999 (fr)
- im Februar 1999 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en febreru de 1999 (ast)
- artikull shkencor i botuar më 01 shkurt 1999 (sq)
- scientific article published on 01 February 1999 (en)
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publication date
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publication date
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author name string
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author name string
| - Hayashi H
- Shiono Y
- Furutsuka K
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rdfs:label
| - Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (en)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (nl)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (sq)
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skos:prefLabel
| - Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (en)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (nl)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (sq)
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name
| - Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (en)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (nl)
- Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (sq)
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title
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title
| - Okaramines H and I, new okaramine congeners, from aspergillus aculeatus (en)
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instance of
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main subject
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main subject
| - Aspergillus aculeatus
- Okaramine A
- Okaramine B
- (4S,5R,14R,15S,16S)-14,16-dihydroxy-15-methoxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetrazaoctacyclo[16.13.0.03,16.04,7.04,14.08,13.022,30.024,29]hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione
- (4S,12R,14R)-12-hydroxy-19,19-dimethyl-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- okaramine H
- (4S,12R,14R)-12-hydroxy-19,19-dimethyl-5-(3-methylbut-2-enyl)-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- (+)-Okaramine J
- Okaramine K_120152
- (1R,4S,7S,9S)-9-hydroxy-4-[[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl]-14-(3-methylbutyl)-2,5,16-triazatetracyclo[7.7.0.02,7.010,15]hexadeca-10,12,14-triene-3,6-dione
- (1Z,4R,12R,14R,17Z)-12-hydroxy-19,19-dimethyl-5-(2-methylbut-3-en-2-yl)-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- (4R,12R,14R)-12-hydroxy-19,19-dimethyl-5-(2-methylbut-3-en-2-yl)-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- (1S,4S,7S,9S)-16-acetyl-4-(1H-indol-3-ylmethyl)-9-(2-methylbut-3-en-2-yl)-2,5,16-triazatetracyclo[7.7.0.02,7.010,15]hexadeca-10,12,14-triene-3,6-dione
- (4S,12R,14R)-12-hydroxy-19,19-dimethyl-5-(2-methylbut-3-en-2-yl)-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- 12-Hydroxy-19,19-dimethyl-5-(3-methylbut-2-enyl)-3,5,16,21-tetrazaheptacyclo[14.13.0.03,14.04,12.06,11.020,28.022,27]nonacosa-1(29),6,8,10,17,20(28),22,24,26-nonaene-2,15-dione
- Okaramine H
- Okaramine I
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is cites work
of | - Fluorous Synthesis of Hydantoin-, Piperazinedione-, and Benzodiazepinedione-Fused Tricyclic and Tetracyclic Ring Systems.
- Fluorous parallel synthesis of a piperazinedione-fused tricyclic compound library
- New and revisited species in Aspergillus section Nigri.
- Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B.
- Dereplication Guided Discovery of Secondary Metabolites of Mixed Biosynthetic Origin from Aspergillus aculeatus
- Asperaculanes A and B, two sesquiterpenoids from the fungus Aspergillus aculeatus.
- Aculeatusquinones A-D, Novel Metabolites from the Marine-Derived Fungus Aspergillus aculeatus
- New Okaramine Congeners, Okamines J, K, L, M and Related Compounds, fromPenicillium simplicissimumATCC 90288
- Okaramines N, O, P, Q and R, new okaramine congeners, from Penicillium simplicissimum ATCC 90288.
- Combined molecular and biochemical approach identifies Aspergillus japonicus and Aspergillus aculeatus as two species
- GluCl a target of indole alkaloid okaramines: a 25 year enigma solved.
- Investigation of a 6-MSA Synthase Gene Cluster in Aspergillus aculeatus Reveals 6-MSA-derived Aculinic Acid, Aculins A-B and Epi-Aculin A.
- Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi.
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