3-Maleimidobenzoic acid N-hydroxysuccinimide ester (BioDeep_00000174869)
human metabolite blood metabolite
代谢物信息卡片
化学式: C15H10N2O6 (314.05388400000004)
中文名称: 3-马来酰亚胺基苯甲酸-N-琥珀酰亚胺酯[交联剂]
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1CC(=O)N(C1=O)OC(=O)C2=CC(=CC=C2)N3C(=O)C=CC3=O
InChI: InChI=1S/C15H10N2O6/c18-11-4-5-12(19)16(11)10-3-1-2-9(8-10)15(22)23-17-13(20)6-7-14(17)21/h1-5,8H,6-7H2
描述信息
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents
同义名列表
11 个代谢物同义名
2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoate; 2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxopyrrol-1-yl)benzoate; 3-Maleimidobenzoic acid N-hydroxysuccinimide ester; m-Maleimidobenzoic acid N-hydroxysuccinimide ester; 3-Maleimidobenzoate N-hydroxysuccinimide ester; 3-Maleimidobenzoyl N-hydroxysuccinimide ester; Meta-maleimidobenzoyl N-hydroxysuccinimide; 3-Maleimidobenzoyl N-hydroxysuccinimide; N-(m-Maleimidobenzoyloxy)succinimide; N-Succinimidyl m-maleimidobenzoate; MBS Crosslinker
数据库引用编号
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
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Journal of microscopy.
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Analytical chemistry.
2003 Nov; 75(21):5797-805. doi:
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Planta.
2001 Feb; 212(3):392-403. doi:
10.1007/s004250000406
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The journal of peptide research : official journal of the American Peptide Society.
2001 Jan; 57(1):1-10. doi:
10.1034/j.1399-3011.2001.00779.x
. [PMID: 11168883] - E Hazum, A Shisheva, Y Shechter. Preparation and application of radioiodinated sulfhydryl reagents for the covalent labeling of SH-proteins present in minute quantities.
Journal of biochemical and biophysical methods.
1992 Mar; 24(1-2):95-106. doi:
10.1016/0165-022x(92)90050-k
. [PMID: 1560185] - Y Okamura, M Yamazaki, T Yamaguchi, Y Komoda, A Sugimoto, H Nakajima. Anti-bilirubin monoclonal antibody. III. Preparation and properties of monoclonal antibodies to unconjugated bilirubin-IX alpha.
Biochimica et biophysica acta.
1991 Apr; 1073(3):538-42. doi:
10.1016/0304-4165(91)90227-8
. [PMID: 2015277] - N Zegers, K Gerritse, C Deen, W Boersma, E Claassen. An improved conjugation method for controlled covalent coupling of synthetic peptides to proteins using glutaraldehyde in a dialysis method.
Journal of immunological methods.
1990 Jul; 130(2):195-200. doi:
10.1016/0022-1759(90)90048-z
. [PMID: 2115551] - R J Edwards, A M Singleton, A R Boobis, D S Davies. Cross-reaction of antibodies to coupling groups used in the production of anti-peptide antibodies.
Journal of immunological methods.
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. [PMID: 2921528] - L D Madison, J D Jamieson, S A Rosenzweig. Heterogeneity of cholecystokinin receptors in pancreas.
Biochemical and biophysical research communications.
1987 Mar; 143(2):761-7. doi:
10.1016/0006-291x(87)91419-7
. [PMID: 3105532] - M S Bernatowicz, G R Matsueda. Preparation of peptide-protein immunogens using N-succinimidyl bromoacetate as a heterobifunctional crosslinking reagent.
Analytical biochemistry.
1986 May; 155(1):95-102. doi:
10.1016/0003-2697(86)90231-9
. [PMID: 3717562] - L D Madison, S A Rosenzweig, J D Jamieson. Use of the heterobifunctional cross-linker m-maleimidobenzoyl N-hydroxysuccinimide ester to affinity label cholecystokinin binding proteins on rat pancreatic plasma membranes.
The Journal of biological chemistry.
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