Maltoheptaose (BioDeep_00000897341)
代谢物信息卡片
化学式: C42H72O36 (1152.3803)
中文名称: 麦芽七糖
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O)O)OC7C(OC(C(C7O)O)O)CO)CO)CO)CO)CO)CO)O)O)O)O
InChI: InChI=1S/C42H72O36/c43-1-8-15(50)16(51)24(59)37(67-8)74-31-10(3-45)69-39(26(61)18(31)53)76-33-12(5-47)71-41(28(63)20(33)55)78-35-14(7-49)72-42(29(64)22(35)57)77-34-13(6-48)70-40(27(62)21(34)56)75-32-11(4-46)68-38(25(60)19(32)54)73-30-9(2-44)66-36(65)23(58)17(30)52/h8-65H,1-7H2/t8-,9-,10-,11-,12-,13-,14-,15-,16+,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36+,37-,38-,39-,40-,41-,42-/m1/s1
描述信息
A maltoheptaose heptasaccharide in which the glucose residue at the reducing end is in the aldehydo open-chain form.
同义名列表
2 个代谢物同义名
Maltoheptaose; 2-[6-[6-[6-[6-[4,5-Dihydroxy-2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:62010
- ChEBI: CHEBI:61954
- ChEBI: CHEBI:143183
- PubChem: 9919918
- PubChem: 13908996
- ChEMBL: CHEMBL3322298
- CAS: 137767-17-0
- CAS: 34620-78-5
- MetaboLights: MTBLC62010
分类词条
相关代谢途径
Reactome(0)
BioCyc(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
- Bai Mingxue, Bai Chaolumen, Daisuke Asai, Hiromu Takemura, Kensuke Miyazaki, Takashi Yoshida. Role of a long-chain alkyl group in sulfated alkyl oligosaccharides with high anti-HIV activity revealed by SPR and DLS.
Carbohydrate polymers.
2020 Oct; 245(?):116518. doi:
10.1016/j.carbpol.2020.116518. [PMID: 32718624] - Joana Gangoiti, Lisa Lamothe, Sander Sebastiaan van Leeuwen, Christina Vafiadi, Lubbert Dijkhuizen. Characterization of the Paenibacillus beijingensis DSM 24997 GtfD and its glucan polymer products representing a new glycoside hydrolase 70 subfamily of 4,6-α-glucanotransferase enzymes.
PloS one.
2017; 12(4):e0172622. doi:
10.1371/journal.pone.0172622. [PMID: 28399167] - Lyann Sim, Sophie R Beeren, Justin Findinier, David Dauvillée, Steven G Ball, Anette Henriksen, Monica M Palcic. Crystal structure of the Chlamydomonas starch debranching enzyme isoamylase ISA1 reveals insights into the mechanism of branch trimming and complex assembly.
The Journal of biological chemistry.
2014 Aug; 289(33):22991-23003. doi:
10.1074/jbc.m114.565044. [PMID: 24993830] - David A Meekins, Madushi Raththagala, Satrio Husodo, Cory J White, Hou-Fu Guo, Oliver Kötting, Craig W Vander Kooi, Matthew S Gentry. Phosphoglucan-bound structure of starch phosphatase Starch Excess4 reveals the mechanism for C6 specificity.
Proceedings of the National Academy of Sciences of the United States of America.
2014 May; 111(20):7272-7. doi:
10.1073/pnas.1400757111. [PMID: 24799671] - Chia-Che Tsai, Chih-Ru Lin, Hsien-Yu Tsai, Chia-Jung Chen, Wen-Tai Li, Hui-Ming Yu, Yi-Yu Ke, Wei-Ying Hsieh, Cheng-Yen Chang, Ying-Ta Wu, Chung-Yi Wu, Shui-Tein Chen, Chi-Huey Wong. The immunologically active oligosaccharides isolated from wheatgrass modulate monocytes via Toll-like receptor-2 signaling.
The Journal of biological chemistry.
2013 Jun; 288(24):17689-97. doi:
10.1074/jbc.m112.448381. [PMID: 23629653] - Jelena Ciric, Katja Loos. Synthesis of branched polysaccharides with tunable degree of branching.
Carbohydrate polymers.
2013 Mar; 93(1):31-7. doi:
10.1016/j.carbpol.2012.04.008. [PMID: 23465898] - Nicole M Koropatkin, Eric C Martens, Jeffrey I Gordon, Thomas J Smith. Starch catabolism by a prominent human gut symbiont is directed by the recognition of amylose helices.
Structure (London, England : 1993).
2008 Jul; 16(7):1105-15. doi:
10.1016/j.str.2008.03.017. [PMID: 18611383] - Elvia García-López, Andrzej Werynski, Olof Heimbürger, José C Divino Filho, Bengt Lindholm, Björn Anderstam. Rate of synthetic oligosaccharide degradation as a novel measure of amylase activity in peritoneal dialysis patients.
Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.
2008 May; 28(3):296-304. doi:
. [PMID: 18474923] - Nicole S Bresolin, Zhongyi Li, Behjat Kosar-Hashemi, Ian J Tetlow, Manash Chatterjee, Sadequr Rahman, Matthew K Morell, Crispin A Howitt. Characterisation of disproportionating enzyme from wheat endosperm.
Planta.
2006 Jun; 224(1):20-31. doi:
10.1007/s00425-005-0187-7. [PMID: 16333636] - Birte Kramhøft, Kristian Sass Bak-Jensen, Haruhide Mori, Nathalie Juge, Jane Nøhr, Birte Svensson. Involvement of individual subsites and secondary substrate binding sites in multiple attack on amylose by barley alpha-amylase.
Biochemistry.
2005 Feb; 44(6):1824-32. doi:
10.1021/bi048100v. [PMID: 15697208] - Christophe Danelon, Thérèse Brando, Mathias Winterhalter. Probing the orientation of reconstituted maltoporin channels at the single-protein level.
The Journal of biological chemistry.
2003 Sep; 278(37):35542-51. doi:
10.1074/jbc.m305434200. [PMID: 12835320] - Olivier Gonçalves, Thierry Dintinger, Dominique Blanchard, Charles Tellier. Functional mimicry between anti-Tendamistat antibodies and alpha-amylase.
Journal of immunological methods.
2002 Nov; 269(1-2):29-37. doi:
10.1016/s0022-1759(02)00238-7. [PMID: 12379350] - Frank Orlik, Christian Andersen, Roland Benz. Site-directed mutagenesis of tyrosine 118 within the central constriction site of the LamB (maltoporin) channel of Escherichia coli. II. Effect on maltose and maltooligosaccharide binding kinetics.
Biophysical journal.
2002 Jul; 83(1):309-21. doi:
10.1016/s0006-3495(02)75171-0. [PMID: 12080122] - J L Rosenblum, G L Hortin, C H Smith, G E Pashos, M Landt. Macroamylases: differences in activity against various-sized substrates.
Clinical chemistry.
1992 Sep; 38(9):1725-9. doi:
. [PMID: 1381999] - J L Rosenblum, G L Hortin, C H Smith, G E Pashos, M Landt. Macroamylases: differences in activity against various-size substrates.
Clinical chemistry.
1992 Aug; 38(8 Pt 1):1454-8. doi:
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Journal of immunological methods.
1988 Sep; 112(2):227-33. doi:
10.1016/0022-1759(88)90362-6. [PMID: 3418128] - E O Haegele, E Schaich, E Rauscher, P Lehmann, M Grassl. Action pattern of human pancreatic alpha-amylase on maltoheptaose, a substrate for determining alpha-amylase in serum.
Journal of chromatography.
1981 Apr; 223(1):69-84. doi:
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