3-Indolylmethyl glucosinolate (BioDeep_00000402815)
natural product PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C16H20N2O9S2 (448.06101900000004)
中文名称:
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 13.16%
分子结构信息
SMILES: C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O
InChI: InChI=1S/C16H20N2O9S2/c19-7-11-13(20)14(21)15(22)16(26-11)28-12(18-27-29(23,24)25)5-8-6-17-10-4-2-1-3-9(8)10/h1-4,6,11,13-17,19-22H,5,7H2,(H,23,24,25)/t11-,13-,14+,15-,16+/m1/s1
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)
0 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
- Antonio Costa-Pérez, Paola Sánchez-Bravo, Sonia Medina, Raúl Domínguez-Perles, Cristina García-Viguera. Bioaccessible Organosulfur Compounds in Broccoli Stalks Modulate the Inflammatory Mediators Involved in Inflammatory Bowel Disease.
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Journal of integrative plant biology.
2021 Dec; 63(12):2058-2074. doi:
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2020 06; 43(6):1571-1583. doi:
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Journal of food science.
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Physiologia plantarum.
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Natural product research.
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. [PMID: 29058468] - Pramod Upadhyaya, Adam T Zarth, Naomi Fujioka, Vincent A Fritz, Stephen S Hecht. Identification and analysis of a mercapturic acid conjugate of indole-3-methyl isothiocyanate in the urine of humans who consumed cruciferous vegetables.
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Molecular nutrition & food research.
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Journal of the science of food and agriculture.
2015 Jul; 95(9):1868-75. doi:
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Journal of the science of food and agriculture.
2015 Feb; 95(3):552-9. doi:
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Journal of medicinal food.
2014 Nov; 17(11):1177-82. doi:
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Oecologia.
2014 Mar; 174(3):893-907. doi:
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Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
2014 Feb; 23(2):282-7. doi:
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Journal of experimental botany.
2014 Feb; 65(2):571-83. doi:
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PloS one.
2014; 9(7):e95683. doi:
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TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik.
2013 Sep; 126(9):2323-34. doi:
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Plant foods for human nutrition (Dordrecht, Netherlands).
2013 Jun; 68(2):113-7. doi:
10.1007/s11130-013-0356-y
. [PMID: 23640295] - Rosa Agneta, Anna Rita Rivelli, Emanuela Ventrella, Filomena Lelario, Giulio Sarli, Sabino Aurelio Bufo. Investigation of glucosinolate profile and qualitative aspects in sprouts and roots of horseradish (Armoracia rusticana) using LC-ESI-hybrid linear ion trap with Fourier transform ion cyclotron resonance mass spectrometry and infrared multiphoton dissociation.
Journal of agricultural and food chemistry.
2012 Aug; 60(30):7474-82. doi:
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. [PMID: 22779710] - Joscelyn Sarsby, Mark W Towers, Chris Stain, Rainer Cramer, Olga A Koroleva. Mass spectrometry imaging of glucosinolates in Arabidopsis flowers and siliques.
Phytochemistry.
2012 May; 77(?):110-8. doi:
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Phytochemistry.
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2011 Dec; 49(12):3287-309. doi:
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Journal of agricultural and food chemistry.
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Organic & biomolecular chemistry.
2010 Nov; 8(22):5150-8. doi:
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Phytochemistry.
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Journal of agricultural and food chemistry.
2004 Dec; 52(25):7607-13. doi:
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The Journal of biological chemistry.
2004 Dec; 279(49):50717-25. doi:
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2003 May; 51(10):3029-34. doi:
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The Plant journal : for cell and molecular biology.
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Phytochemistry.
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