Antifungal alkaloids and limonoid derivatives from Dictamnus dasycarpus
Two furoquinoline alkaloids and four limonoid derivatives isolated from the root bark of Dictamnus dasycarpus (Rutaceae) showed inhibitory activity against the plant pathogenic fungus Cladosporium cucumerinum. From the root bark of Dictamnus dasycarpus (Rutaceae), four limonoid derivatives, two furo...
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| Veröffentlicht in: | Phytochemistry (Oxford) 1998, Vol.47 (1), p.7-11 |
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| creator | Zhao, Weimin Wolfender, Jean-Luc Hostettmann, Kurt Xu, Rensheng Qin, Guowei |
| description | Two furoquinoline alkaloids and four limonoid derivatives isolated from the root bark of
Dictamnus dasycarpus (Rutaceae) showed inhibitory activity against the plant pathogenic fungus
Cladosporium cucumerinum.
From the root bark of
Dictamnus dasycarpus (Rutaceae), four limonoid derivatives, two furoquinoline alkaloids, five limonoids, two sesquiterpenes and three steroids were isolated and their structures elucidated on the basis of various spectroscopic methods. Among the identified compounds, one was determined to be a new natural product, 6β-hydroxyfraxinellone, while six compounds were found to be active against the plant pathogenic fungus
Cladosporium cucumerinum. The relationship between the structures of limonoid derivatives and their inhibitory activity against fungal growth was investigated. |
| doi_str_mv | 10.1016/S0031-9422(97)00541-4 |
| format | Article |
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Dictamnus dasycarpus (Rutaceae) showed inhibitory activity against the plant pathogenic fungus
Cladosporium cucumerinum.
From the root bark of
Dictamnus dasycarpus (Rutaceae), four limonoid derivatives, two furoquinoline alkaloids, five limonoids, two sesquiterpenes and three steroids were isolated and their structures elucidated on the basis of various spectroscopic methods. Among the identified compounds, one was determined to be a new natural product, 6β-hydroxyfraxinellone, while six compounds were found to be active against the plant pathogenic fungus
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Dictamnus dasycarpus (Rutaceae) showed inhibitory activity against the plant pathogenic fungus
Cladosporium cucumerinum.
From the root bark of
Dictamnus dasycarpus (Rutaceae), four limonoid derivatives, two furoquinoline alkaloids, five limonoids, two sesquiterpenes and three steroids were isolated and their structures elucidated on the basis of various spectroscopic methods. Among the identified compounds, one was determined to be a new natural product, 6β-hydroxyfraxinellone, while six compounds were found to be active against the plant pathogenic fungus
Cladosporium cucumerinum. The relationship between the structures of limonoid derivatives and their inhibitory activity against fungal growth was investigated.</description><subject>Alkaloids - chemistry</subject><subject>Alkaloids - isolation & purification</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Chemical control</subject><subject>Control</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Molecular Structure</subject><subject>Phytopathology. Animal pests. 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Psychology</topic><topic>Fungal plant pathogens</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Molecular Structure</topic><topic>Phytopathology. Animal pests. 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Dictamnus dasycarpus (Rutaceae) showed inhibitory activity against the plant pathogenic fungus
Cladosporium cucumerinum.
From the root bark of
Dictamnus dasycarpus (Rutaceae), four limonoid derivatives, two furoquinoline alkaloids, five limonoids, two sesquiterpenes and three steroids were isolated and their structures elucidated on the basis of various spectroscopic methods. Among the identified compounds, one was determined to be a new natural product, 6β-hydroxyfraxinellone, while six compounds were found to be active against the plant pathogenic fungus
Cladosporium cucumerinum. The relationship between the structures of limonoid derivatives and their inhibitory activity against fungal growth was investigated.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>9429316</pmid><doi>10.1016/S0031-9422(97)00541-4</doi><tpages>5</tpages></addata></record> |
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| ispartof | Phytochemistry (Oxford), 1998, Vol.47 (1), p.7-11 |
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| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | Alkaloids - chemistry Alkaloids - isolation & purification Antifungal Agents - chemistry Antifungal Agents - isolation & purification Biological and medical sciences Biotechnology Chemical control Control Fundamental and applied biological sciences. Psychology Fungal plant pathogens Magnetic Resonance Spectroscopy Molecular Structure Phytopathology. Animal pests. Plant and forest protection Triterpenes - chemistry Triterpenes - isolation & purification |
| title | Antifungal alkaloids and limonoid derivatives from Dictamnus dasycarpus |
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