Succinimide (BioDeep_00000003420)
Secondary id: BioDeep_00001868191
human metabolite natural product
代谢物信息卡片
化学式: C4H5NO2 (99.032)
中文名称: 琥珀酰亚胺, 丁二酰亚胺
谱图信息:
最多检出来源 Homo sapiens(natural_products) 24.12%
Last reviewed on 2024-06-29.
Cite this Page
Succinimide. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/succinimide (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000003420). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C1CC(=O)NC1=O
InChI: InChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)
描述信息
Succinimide is an organic compound with the formula (CH2)2(CO)2NH. This white solid is used in a variety of organic syntheses, as well as in some industrial silver plating processes. The compound is classified as a cyclic imide. It may be prepared by thermal decomposition of ammonium succinate.[4]
Succinimide, also known as butanimide, belongs to the class of organic compounds known as pyrrolidine-2-ones. These are pyrrolidines that bear a C=O group at position 2 of the pyrrolidine ring. Succinimide has been identified in urine (PMID: 22409530).
Succinimides refers to compounds that contain the succinimide group. These compounds have some notable uses. Several succinimides are used as anticonvulsant drugs, including ethosuximide, phensuximide, and methsuximide.[5]
Succinimides are also used to form covalent bonds between proteins or peptides and plastics, which is useful in a variety of assay techniques.
Succinimide. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=123-56-8 (retrieved 2024-06-29) (CAS RN: 123-56-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:9307
- KEGG: C07273
- KEGGdrug: D08532
- PubChem: 11439
- HMDB: HMDB0240653
- Metlin: METLIN66615
- DrugBank: DB13376
- ChEMBL: CHEMBL275661
- Wikipedia: Succinimide
- chemspider: 10955
- CAS: 123-56-8
- MoNA: KO001803
- MoNA: KO001804
- MoNA: KO001805
- MoNA: KO001806
- MoNA: KO001802
- PMhub: MS000009649
- NIKKAJI: J25.395B
- RefMet: Succinimide
- LOTUS: LTS0005145
- PubChem: 9482
- KNApSAcK: 9307
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)
14 个相关的物种来源信息
- 4050 - Araliaceae: LTS0005145
- 4210 - Asteraceae: LTS0005145
- 2759 - Eukaryota: LTS0005145
- 9606 - Homo sapiens: -
- 3398 - Magnoliopsida: LTS0005145
- 4053 - Panax: LTS0005145
- 44586 - Panax notoginseng: 10.1021/JF301835V
- 44586 - Panax notoginseng: LTS0005145
- 35493 - Streptophyta: LTS0005145
- 58023 - Tracheophyta: LTS0005145
- 33090 - Viridiplantae: LTS0005145
- 36590 - Xanthium: LTS0005145
- 318068 - Xanthium strumarium: 10.1055/S-2008-1081295
- 318068 - Xanthium strumarium: LTS0005145
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
- Jeningsih, Ling Ling Tan, Alizar Ulianas, Lee Yook Heng, Nur-Fadhilah Mazlan, Nur Diyana Jamaluddin, Nurul Yuziana Mohd Yusof, Bahariah Khalid, Goh Choo Ta. Sandwich-Type DNA Micro-Optode Based on Gold-Latex Spheres Label for Reflectance Dengue Virus Detection.
Sensors (Basel, Switzerland).
2020 Mar; 20(7):. doi:
10.3390/s20071820
. [PMID: 32218202] - Mingyan Cao, Weichen Xu, Ben Niu, Ivy Kabundi, Haibin Luo, Meagan Prophet, Weimin Chen, Dengfeng Liu, Sergei V Saveliev, Marjeta Urh, Jihong Wang. An Automated and Qualified Platform Method for Site-Specific Succinimide and Deamidation Quantitation Using Low-pH Peptide Mapping.
Journal of pharmaceutical sciences.
2019 11; 108(11):3540-3549. doi:
10.1016/j.xphs.2019.07.019
. [PMID: 31374319] - Bing Yang, Haifan Wu, Paul D Schnier, Yansheng Liu, Jun Liu, Nanxi Wang, William F DeGrado, Lei Wang. Proximity-enhanced SuFEx chemical cross-linker for specific and multitargeting cross-linking mass spectrometry.
Proceedings of the National Academy of Sciences of the United States of America.
2018 10; 115(44):11162-11167. doi:
10.1073/pnas.1813574115
. [PMID: 30322930] - Melanie Derde, Véronique Vié, Astrid Walrant, Sandrine Sagan, Valérie Lechevalier, Catherine Guérin-Dubiard, Stéphane Pezennec, Marie-Françoise Cochet, Gilles Paboeuf, Maryvonne Pasco, Florence Baron, Michel Gautier, Sophie Jan, Françoise Nau. Antimicrobial activity of lysozyme isoforms: Key molecular features.
Biopolymers.
2017 Dec; 107(12):. doi:
10.1002/bip.23040
. [PMID: 28944959] - Peter Bults, Rainer Bischoff, Hilde Bakker, Jourik A Gietema, Nico C van de Merbel. LC-MS/MS-Based Monitoring of In Vivo Protein Biotransformation: Quantitative Determination of Trastuzumab and Its Deamidation Products in Human Plasma.
Analytical chemistry.
2016 Feb; 88(3):1871-7. doi:
10.1021/acs.analchem.5b04276
. [PMID: 26713683] - John C Lainson, Mariana Ferrer Fuenmayor, Stephen Albert Johnston, Chris W Diehnelt. Conjugation Approach To Produce a Staphylococcus aureus Synbody with Activity in Serum.
Bioconjugate chemistry.
2015 Oct; 26(10):2125-32. doi:
10.1021/acs.bioconjchem.5b00420
. [PMID: 26365100] - D V Krupenya, P A Snegurov, E V Grachova, V V Gurzhiy, S P Tunik, A S Melnikov, P Yu Serdobintsev, E G Vlakh, E S Sinitsyna, T B Tennikova. New supramolecular Au(I)-Cu(I) complex as potential luminescent label for proteins.
Inorganic chemistry.
2013 Nov; 52(21):12521-8. doi:
10.1021/ic401569n
. [PMID: 24134597] - David Ouellette, Chris Chumsae, Anca Clabbers, Czeslaw Radziejewski, Ivan Correia. Comparison of the in vitro and in vivo stability of a succinimide intermediate observed on a therapeutic IgG1 molecule.
mAbs.
2013 May; 5(3):432-44. doi:
10.4161/mabs.24458
. [PMID: 23608772] - Sujeet K Mishra, Devendra Kumar, Ashok M Biradar, Rajesh. Electrochemical impedance spectroscopy characterization of mercaptopropionic acid capped ZnS nanocrystal based bioelectrode for the detection of the cardiac biomarker--myoglobin.
Bioelectrochemistry (Amsterdam, Netherlands).
2012 Dec; 88(?):118-26. doi:
10.1016/j.bioelechem.2012.07.006
. [PMID: 22922532] - Cassie J Fhaner, Sichang Liu, Hong Ji, Richard J Simpson, Gavin E Reid. Comprehensive lipidome profiling of isogenic primary and metastatic colon adenocarcinoma cell lines.
Analytical chemistry.
2012 Nov; 84(21):8917-26. doi:
10.1021/ac302154g
. [PMID: 23039336] - Abhishek Sharma, Naina Sharma, Rakesh Kumar, Upendra K Sharma, Arun K Sinha. Water-promoted cascade synthesis of alpha-arylaldehydes from arylalkenes using N-halosuccinimides: an avenue for asymmetric oxidation using Cinchona organocatalysis.
Chemical communications (Cambridge, England).
2009 Sep; ?(35):5299-301. doi:
10.1039/b908717f
. [PMID: 19707652] - Rong-Min Wang, Teruyuki Komatsu, Akito Nakagawa, Eishun Tsuchida. Human serum albumin bearing covalently attached iron(II) porphyrins as O2-coordination sites.
Bioconjugate chemistry.
2005 Jan; 16(1):23-6. doi:
10.1021/bc049859m
. [PMID: 15656571] - Gary O Rankin. Nephrotoxicity induced by C- and N-arylsuccinimides.
Journal of toxicology and environmental health. Part B, Critical reviews.
2004 Sep; 7(5):399-416. doi:
10.1080/10937400490486113
. [PMID: 15371242] - Ammar Azioune, Amel Ben Slimane, Lobnat Ait Hamou, Anne Pleuvy, Mohamed M Chehimi, Christian Perruchot, Steven P Armes. Synthesis and characterization of active ester-functionalized polypyrrole-silica nanoparticles: application to the covalent attachment of proteins.
Langmuir : the ACS journal of surfaces and colloids.
2004 Apr; 20(8):3350-6. doi:
10.1021/la030407s
. [PMID: 15875868] - E F Bandle, G Wendt, U B Ranalder, K H Trautmann. 2-Pyrrolidinone and succinimide endogenously present in several mammalian species.
Life sciences.
1984 Nov; 35(22):2205-12. doi:
10.1016/0024-3205(84)90461-2
. [PMID: 6503611] - M R Eftink, C A Ghiron. Fluorescence quenching studies with proteins.
Analytical biochemistry.
1981 Jul; 114(2):199-227. doi:
10.1016/0003-2697(81)90474-7
. [PMID: 7030122]