2-Pyrol (BioDeep_00000865879)
Main id: BioDeep_00000017741
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C4H7NO (85.0527612)
中文名称: 2-吡咯烷酮
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1CC(=O)NC1
InChI: InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)
描述信息
同义名列表
42 个代谢物同义名
Hydrogen tribromide, compound with pyrrolidin-2-one (1:3); InChI=1\C4H7NO\c6-4-2-1-3-5-4\h1-3H2,(H,5,6; Butanoic acid, 4-amino-, lactam; gamma-Aminobutyric acid lactam; 2-PYRROLIDONE MFC4 H7 N1 O1; .gamma.-Aminobutyric lactam; 4-Aminobutyric acid lactam; gamma-Aminobutyric lactam; .gamma.-Aminobutyrolactam; gamma-Aminobutyrolactam; .alpha.-Pyrrolidinone; .gamma.-Butyrolactam; Pyrrolidon [German]; .alpha.-Pyrrolidone; alpha-Pyrrolidinone; gamma-Butyrolactam; alpha-Pyrrolidone; 2-Ketopyrrolidine; 2-Oxopyrrolidine; pyrrolidin-2-one; EINECS 210-483-1; EINECS 245-100-7; 2-Pyrrolidinone; NCIOpen2_000687; 240338_ALDRICH; P74370_ALDRICH; 2-pyrrolidone; ZINC04759215; Butyrolactam; CHEBI:36592; WLN: T5MVTJ; 83300_FLUKA; Pyrrolidone; 22580-55-8; Pyrrolidon; HSDB 2652; NSC 4593; NSC 8413; 616-45-5; NSC4593; NSC8413; 2-Pyrol
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)
6 个相关的物种来源信息
- 107450 - Ascochyta medicaginicola: 10.1371/JOURNAL.PONE.0206641
- 65558 - Capparis spinosa: 10.1021/JF302075W
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 1089418 - Microtropis japonica: 10.1021/NP800097T
- 29760 - Vitis vinifera:
- 33090 - 砂仁: -
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
- Zongde Jiang, Feng Zhou, Huixia Huo, Zisheng Han, Chunyin Qin, Chi-Tang Ho, Liang Zhang, Xiaochun Wan. Formation Mechanism of Di-N-ethyl-2-pyrrolidinone-Substituted Epigallocatechin Gallate during High-Temperature Roasting of Tea.
Journal of agricultural and food chemistry.
2023 Feb; 71(6):2975-2989. doi:
10.1021/acs.jafc.2c07071
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Journal of agricultural and food chemistry.
2022 Mar; 70(12):3832-3841. doi:
10.1021/acs.jafc.2c00798
. [PMID: 35289174] - Shi-Yu Liu, Yuan-Yuan Zhang, Gang-Xiu Chu, Guan-Hu Bao. N-ethyl-2-pyrrolidinone substitution enhances binding affinity between tea flavoalkaloids and human serum albumin: Greatly influenced by esterization.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2021 Dec; 262(?):120097. doi:
10.1016/j.saa.2021.120097
. [PMID: 34182296] - Weidong Dai, Maria Ramos-Jerz, Dongchao Xie, Jiakun Peng, Peter Winterhalter, Gerold Jerz, Zhi Lin. Isolation of N-Ethyl-2-pyrrolidinone-Substituted Flavanols from White Tea Using Centrifugal Countercurrent Chromatography Off-Line ESI-MS Profiling and Semi-Preparative Liquid Chromatography.
Molecules (Basel, Switzerland).
2021 Nov; 26(23):. doi:
10.3390/molecules26237284
. [PMID: 34885862] - Weidong Dai, Ni Lou, Dongchao Xie, Zhengyan Hu, Huiyi Song, Meiling Lu, Dong Shang, Wenliang Wu, Jiakun Peng, Peiyuan Yin, Zhi Lin. N-Ethyl-2-Pyrrolidinone-Substituted Flavan-3-Ols with Anti-inflammatory Activity in Lipopolysaccharide-Stimulated Macrophages Are Storage-Related Marker Compounds for Green Tea.
Journal of agricultural and food chemistry.
2020 Oct; 68(43):12164-12172. doi:
10.1021/acs.jafc.0c03952
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2020 01; 15(1):226-233. doi:
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2011 Jul; 9(?):102. doi:
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2011 May; 409(1-2):89-95. doi:
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Bioorganic & medicinal chemistry.
2011 May; 19(9):2888-902. doi:
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2011; 2(?):101. doi:
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