Fenpropimorph (BioDeep_00000001154)
Secondary id: BioDeep_00000397708
human metabolite Endogenous
代谢物信息卡片
化学式: C20H33NO (303.25620080000004)
中文名称: 顺-4-叔丁基苯基(-2-甲基丙基)-2,6-二甲基吗啉, 丁苯吗琳
谱图信息:
最多检出来源 Viridiplantae(plant) 22.22%
分子结构信息
SMILES: CC(Cc1ccc(C(C)(C)C)cc1)CN1CC(C)OC(C)C1
InChI: InChI=1S/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3
描述信息
Fenpropimorph (CAS: 67564-91-4) belongs to the class of organic compounds known as phenylpropanes. These are organic compounds containing a phenylpropane moiety. Fenpropimorph is possibly neutral. Fenpropimorph is an agricultural fungicide used against powdery mildews on sugar beets, beans, and leek.
Agricultural fungicide used against powdery mildews on sugar beet, beans and leeks
CONFIDENCE standard compound; INTERNAL_ID 8406
CONFIDENCE standard compound; INTERNAL_ID 2573
D016573 - Agrochemicals
D010575 - Pesticides
同义名列表
12 个代谢物同义名
(2R,6S)-4-[(2S)-3-[4-(1,1-Dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; (2R,6S)-4-[(2S)-2-[(4-tert-butylphenyl)methyl]propyl]-2,6-dimethylmorpholine; 4-[3-[4-(1,1-Dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholine; cis-4-[3-(4-Tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine; (S)-(-)-Fenpropimorph; (S)-cis-Fenpropimorph; cis-Fenpropimorph; (S)-Fenpropimorph; Fenpropimorph; power task; Fenpropimorph; Fenpropimorph
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:143732
- ChEBI: CHEBI:50146
- KEGG: C18787
- PubChem: 11833620
- PubChem: 93365
- PubChem: 91695
- HMDB: HMDB0037270
- Metlin: METLIN6301
- ChEMBL: CHEMBL372700
- Wikipedia: Fenpropimorph
- foodb: FDB016288
- chemspider: 10008267
- CAS: 76492-90-5
- CAS: 67306-03-0
- CAS: 67564-91-4
- MoNA: AU257304
- MoNA: AU257306
- MoNA: AU257301
- MoNA: AU257305
- MoNA: SM840601
- MoNA: AU257303
- MoNA: AU257302
- PMhub: MS000000053
- ChEBI: CHEBI:50145
- PubChem: 124489461
- KNApSAcK: 50145
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Nathalie Bonvallot, Cécile Canlet, Florence Blas-Y-Estrada, Roselyne Gautier, Marie Tremblay-Franco, Sylvie Chevolleau, Sylvaine Cordier, Jean-Pierre Cravedi. Metabolome disruption of pregnant rats and their offspring resulting from repeated exposure to a pesticide mixture representative of environmental contamination in Brittany.
PloS one.
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Mycorrhiza.
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Pest management science.
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Phytochemistry.
2008 Dec; 69(17):2912-9. doi:
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Mycological research.
2008 May; 112(Pt 5):592-601. doi:
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2007 Nov; 282(45):32935-48. doi:
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Plant physiology.
2007 Jan; 143(1):461-72. doi:
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. [PMID: 17114270] - Minze Leistra, Johan H Smelt, J Hilbrand Weststrate, Frederik van den Berg, René Aalderink. Volatilization of the pesticides chlorpyrifos and fenpropimorph from a potato crop.
Environmental science & technology.
2006 Jan; 40(1):96-102. doi:
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Plant molecular biology.
2005 Mar; 57(5):693-707. doi:
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Plant physiology.
2003 Mar; 131(3):1258-69. doi:
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. [PMID: 12644676] - Marie-Andrée Hartmann, Anne-Marie Perret, Jean-Pierre Carde, Claude Cassagne, Patrick Moreau. Inhibition of the sterol pathway in leek seedlings impairs phosphatidylserine and glucosylceramide synthesis but triggers an accumulation of triacylglycerols.
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