dextrose (BioDeep_00000405557)
Main id: BioDeep_00000014321
natural product PANOMIX_OTCML-2023 BioNovoGene_Lab2019
代谢物信息卡片
化学式: C6H12O6 (180.0634)
中文名称: α-D-葡萄糖, 葡萄糖
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C(C1C(C(C(C(O1)O)O)O)O)O
InChI: InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
描述信息
COVID info from COVID-19 Disease Map, PDB, Protein Data Bank
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
alpha-D-glucose is an endogenous metabolite.
alpha-D-glucose is an endogenous metabolite.
同义名列表
5 个代谢物同义名
Grape sugar; dextrose; alpha-D-Glucose; alpha-D-Glucose; Hexose
数据库引用编号
25 个数据库交叉引用编号
- ChEBI: CHEBI:18398
- ChEBI: CHEBI:28102
- ChEBI: CHEBI:18269
- ChEBI: CHEBI:15444
- ChEBI: CHEBI:17925
- ChEBI: CHEBI:28100
- KEGG: C00267
- KEGGdrug: D70945
- PubChem: 79025
- ChEMBL: CHEMBL423707
- CAS: 26655-34-5
- CAS: 27707-45-5
- CAS: 492-62-6
- MoNA: CCMSLIB00005463619
- MoNA: HMDB0003345_ms_ms_2254
- MoNA: HMDB0003345_ms_ms_2255
- PubChem: 3565
- KNApSAcK: C00001122
- PDB-CCD: GLC
- 3DMET: B01203
- NIKKAJI: J44.217H
- medchemexpress: HY-128417
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-544
- KNApSAcK: 17925
- LOTUS: LTS0241274
分类词条
相关代谢途径
Reactome(27)
- Metabolism
- Metabolism of proteins
- Post-translational protein modification
- Disease
- Asparagine N-linked glycosylation
- Metabolism of lipids
- Transport of small molecules
- SLC-mediated transmembrane transport
- Mycobacterium tuberculosis biological processes
- Disorders of transmembrane transporters
- SLC transporter disorders
- Glycolysis
- Carbohydrate metabolism
- Glucose metabolism
- Integration of energy metabolism
- Glycogen metabolism
- Glycogen breakdown (glycogenolysis)
- Gluconeogenesis
- Lactose synthesis
- Sphingolipid metabolism
- Glycosphingolipid metabolism
- Transport to the Golgi and subsequent modification
- Digestion and absorption
- Digestion
- Digestion of dietary carbohydrate
- Trehalose biosynthesis
- Glycosphingolipid catabolism
BioCyc(11)
- chitin biosynthesis
- trehalose degradation II (cytosolic)
- sucrose degradation II (sucrose synthase)
- superpathway of anaerobic sucrose degradation
- protein N-glycosylation processing phase (mammalian)
- protein N-glycosylation processing phase (plants and animals)
- UDP-galactose biosynthesis
- trehalose degradation
- trehalose degradation VI (periplasmic)
- trehalose degradation V
- trehalose degradation II (trehalase)
PlantCyc(6)
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)
103 个相关的物种来源信息
- 4185 - Acanthaceae: LTS0241274
- 531827 - Aesculus chinensis var. wilsonii: 10.1055/S-0028-1097463
- 231459 - Afraegle: LTS0241274
- 231460 - Afraegle paniculata: 10.1039/JR9610005234
- 231460 - Afraegle paniculata: LTS0241274
- 4678 - Allium: LTS0241274
- 166816 - Allium obliquum: 10.1515/ZNB-1967-0633
- 166816 - Allium obliquum: LTS0241274
- 4668 - Amaryllidaceae: LTS0241274
- 262982 - Artemisia apiacea: 10.1016/J.CHROMA.2007.09.023
- 496566 - Artemisia carvifolia: 10.1016/J.CHROMA.2007.09.023
- 6656 - Arthropoda: LTS0241274
- 4890 - Ascomycota: LTS0241274
- 40552 - Asparagaceae: LTS0241274
- 4685 - Asparagus: LTS0241274
- 4686 - Asparagus officinalis: 10.1021/JA02215A010
- 4686 - Asparagus officinalis: LTS0241274
- 1131492 - Aspergillaceae: LTS0241274
- 4210 - Asteraceae: LTS0241274
- 3208 - Bryophyta: LTS0241274
- 3214 - Bryopsida: LTS0241274
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 43460 - Cephalanthus: LTS0241274
- 43461 - Cephalanthus occidentalis: 10.1055/S-2005-864103
- 43461 - Cephalanthus occidentalis: LTS0241274
- 3166 - Chlorophyceae: LTS0241274
- 3041 - Chlorophyta: LTS0241274
- 30102 - Cicadellidae: LTS0241274
- 54221 - Clerodendrum mandarinorum: 10.1055/S-2006-957923
- 41218 - Colchicaceae: LTS0241274
- 6669 - Daphnia pulex: 10.1038/SREP25125
- 327901 - Detarium microcarpum: 10.1016/S0008-6215(02)00025-3
- 2759 - Eukaryota: LTS0241274
- 212961 - Euphorbia plumerioides: 10.1016/0031-9422(91)84139-J
- 147545 - Eurotiomycetes: LTS0241274
- 3803 - Fabaceae: LTS0241274
- 3216 - Funariaceae: LTS0241274
- 4751 - Fungi: LTS0241274
- 92911 - Galactites tomentosus: 10.1007/S10600-017-2003-6
- 41219 - Gloriosa: LTS0241274
- 41220 - Gloriosa superba: 10.1039/CT9150700835
- 41220 - Gloriosa superba: LTS0241274
- 50557 - Insecta: LTS0241274
- 4190 - Justicia: LTS0241274
- 141317 - Justicia adhatoda: 10.1016/S0031-9422(00)83845-5
- 141317 - Justicia adhatoda: LTS0241274
- 495256 - Lagotis brevituba: 10.1055/S-2006-959389
- 3325 - Larix: LTS0241274
- 3326 - Larix laricina: 10.1139/V60-037
- 3326 - Larix laricina: LTS0241274
- 4677 - Liliaceae: LTS0241274
- 4447 - Liliopsida: LTS0241274
- 3398 - Magnoliopsida: LTS0241274
- 33208 - Metazoa: LTS0241274
- 43521 - Morinda: LTS0241274
- 43522 - Morinda citrifolia:
- 43522 - Morinda citrifolia: 10.1021/NP0495985
- 43522 - Morinda citrifolia: LTS0241274
- 72958 - Olearia: LTS0241274
- 199265 - Olearia paniculata: 10.1071/CH9640712
- 199265 - Olearia paniculata: LTS0241274
- 2699671 - Ouratea semiserrata: 10.1002/PCA.656
- 1822464 - Paraburkholderia: 10.1128/AEM.01851-20
- 3683 - Passifloraceae: LTS0241274
- 5073 - Penicillium: LTS0241274
- 5076 - Penicillium chrysogenum: 10.1016/S0021-9673(01)98382-7
- 5076 - Penicillium chrysogenum: LTS0241274
- 3883 - Phaseolus: LTS0241274
- 3885 - Phaseolus vulgaris: 10.1515/BCHM2.1910.68.2.93
- 3885 - Phaseolus vulgaris: LTS0241274
- 572115 - Phlomoides rotata: 10.1002/PCA.2557
- 42345 - Phoenix dactylifera: 10.1016/B978-0-08-028853-6.50009-7
- 3217 - Physcomitrella: LTS0241274
- 3318 - Pinaceae: LTS0241274
- 58019 - Pinopsida: LTS0241274
- 3887 - Pisum: LTS0241274
- 3888 - Pisum sativum: 10.1515/BCHM2.1910.68.2.93
- 3888 - Pisum sativum: LTS0241274
- 170927 - Primula veris: 10.1055/S-0028-1099459
- 418402 - Pseudostellaria heterophylla: 10.3390/MOLECULES21111538
- 4060 - Rauvolfia serpentina: 10.1002/HLCA.19940770809
- 24966 - Rubiaceae: LTS0241274
- 441006 - Ruellia patula: 10.3109/13880209309082928
- 23513 - Rutaceae: LTS0241274
- 28901 - Salmonella enterica: 10.1039/C3MB25598K
- 2026527 - Salvia rhyacophila: 10.1016/S0031-9422(00)90671-X
- 3086 - Scenedesmaceae: LTS0241274
- 3087 - Scenedesmus: LTS0241274
- 104103 - Scenedesmus acutus: LTS0241274
- 35493 - Streptophyta: LTS0241274
- 91192 - Tetradesmus: LTS0241274
- 3088 - Tetradesmus obliquus: LTS0241274
- 58023 - Tracheophyta: LTS0241274
- 28568 - Trichocomaceae: LTS0241274
- 13305 - Tulipa: LTS0241274
- 89494 - Tulipa turkestanica: 10.1016/S0031-9422(98)00716-X
- 89494 - Tulipa turkestanica: LTS0241274
- 45183 - Turnera: LTS0241274
- 329212 - Turnera diffusa: 10.1021/NP060253R
- 329212 - Turnera diffusa: LTS0241274
- 45182 - Turneraceae: LTS0241274
- 33090 - Viridiplantae: LTS0241274
- 126910 - Withania somnifera:
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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- Yusuke Matsumoto, Yukiko Enomoto, Satoshi Kimura, Tadahisa Iwata. Highly deformable and recoverable cross-linked hydrogels of 1,3-α-d and 1,3-β-d-glucans.
Carbohydrate polymers.
2021 Jan; 251(?):116794. doi:
10.1016/j.carbpol.2020.116794
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Pathogens and disease.
2020 12; 78(9):. doi:
10.1093/femspd/ftaa062
. [PMID: 33232457] - Ryan Shaktah, Laura Vardanyan, Elroma David, Alexis Aleman, Dupre Orr, Lawrence A Shaktah, Daniel Tamae, Thomas Minehan. Synthesis and Stereochemical Assignment of Conioidine A: DNA- and HSA-Binding Studies of the Four Diastereomers.
Journal of natural products.
2020 10; 83(10):3191-3198. doi:
10.1021/acs.jnatprod.0c00871
. [PMID: 33034450] - Qinfeng He, Ryosuke Kusumi, Satoshi Kimura, Ung-Jin Kim, Kenzo Deguchi, Shinobu Ohki, Atsushi Goto, Tadashi Shimizu, Masahisa Wada. Highly swellable hydrogel of regioselectively aminated (1→3)-α-d-glucan crosslinked with ethylene glycol diglycidyl ether.
Carbohydrate polymers.
2020 Jun; 237(?):116189. doi:
10.1016/j.carbpol.2020.116189
. [PMID: 32241412] - Kayoko Kobayashi, Takuto Hasegawa, Ryosuke Kusumi, Satoshi Kimura, Makoto Yoshida, Junji Sugiyama, Masahisa Wada. Characterization of crystalline linear (1→3)-α-d-glucan synthesized in vitro.
Carbohydrate polymers.
2017 Dec; 177(?):341-346. doi:
10.1016/j.carbpol.2017.09.003
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Medical mycology journal.
2017; 58(4):E121-E129. doi:
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Scientific reports.
2016 07; 6(?):30479. doi:
10.1038/srep30479
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Molecules (Basel, Switzerland).
2016 Jul; 21(8):. doi:
10.3390/molecules21080980
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Immunopharmacology and immunotoxicology.
2012 Dec; 34(6):907-11. doi:
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Glycobiology.
2012 Oct; 22(10):1282-8. doi:
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Molecular biology reports.
2012 Sep; 39(9):8955-64. doi:
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2012 Jul; 18(7):966-73. doi:
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Archives of pharmacal research.
2012 Jun; 35(6):1021-35. doi:
10.1007/s12272-012-0610-0
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2012 May; 37(10):1422-5. doi:
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The FEBS journal.
2012 May; 279(9):1545-62. doi:
10.1111/j.1742-4658.2011.08469.x
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Plant methods.
2012 Apr; 8(?):13. doi:
10.1186/1746-4811-8-13
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Pharmacognosy research.
2012 Apr; 4(2):116-22. doi:
10.4103/0974-8490.94737
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Nanoscale.
2012 Mar; 4(6):1910-8. doi:
10.1039/c1nr11224d
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Archives of pharmacal research.
2012 Mar; 35(3):415-21. doi:
10.1007/s12272-012-0303-8
. [PMID: 22477187] - Mamtimin Batur, Upur Halmurat, Fu-Hua Hao, Rena Aiziz, Matsidik Aynur. Correlative analysis of neoplasm patients with phlegm-stasis or abnormal Savda syndrome, based on metabonomics.
Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan.
2012 Mar; 32(1):119-24. doi:
10.1016/s0254-6272(12)60044-2
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Applied biochemistry and biotechnology.
2012 Feb; 166(3):523-35. doi:
10.1007/s12010-011-9445-2
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Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering.
2012; 47(4):577-88. doi:
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Current medicinal chemistry.
2012; 19(28):4869-74. doi:
10.2174/092986712803341502
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Clinics (Sao Paulo, Brazil).
2012; 67(4):363-73. doi:
10.6061/clinics/2012(04)10
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Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.
2012 Jan; 24(1):90-5. doi:
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Frontiers in plant science.
2012; 3(?):24. doi:
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PloS one.
2012; 7(7):e40618. doi:
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Pharmacognosy magazine.
2012 Jan; 8(29):12-5. doi:
10.4103/0973-1296.93303
. [PMID: 22438657] - Anke Reinders, Alicia B Sivitz, John M Ward. Evolution of plant sucrose uptake transporters.
Frontiers in plant science.
2012; 3(?):22. doi:
10.3389/fpls.2012.00022
. [PMID: 22639641] - R Grempler, L Thomas, M Eckhardt, F Himmelsbach, A Sauer, D E Sharp, R A Bakker, M Mark, T Klein, P Eickelmann. Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors.
Diabetes, obesity & metabolism.
2012 Jan; 14(1):83-90. doi:
10.1111/j.1463-1326.2011.01517.x
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PLoS neglected tropical diseases.
2012; 6(3):e1583. doi:
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Journal of pharmaceutical and biomedical analysis.
2011 Dec; 56(5):880-6. doi:
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Natural product communications.
2011 Dec; 6(12):1893-6. doi:
"
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Experimental gerontology.
2011 Oct; 46(10):787-93. doi:
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Archives of pharmacal research.
2011 Oct; 34(10):1587-91. doi:
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Journal of young pharmacists : JYP.
2011 Oct; 3(4):267-74. doi:
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Acta microbiologica et immunologica Hungarica.
2011 Sep; 58(3):201-9. doi:
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. [PMID: 21983321] - Ling Wang, Chaofeng Zhang, Mara Layba, Mian Zhang. [Triterpenes and sterols from Nauclea latifolia].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2011 Sep; 36(18):2511-4. doi:
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Archives of pharmacal research.
2011 Aug; 34(8):1283-8. doi:
10.1007/s12272-011-0807-7
. [PMID: 21910049] - Sheng Lin, Zhongxiao Zhang, Yunheng Shen, Huiliang Li, Lei Shan, Runhui Liu, Xike Xu, Weidong Zhang. [One new lignan glycoside from whole plants of Senecio chrysanthemoides].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2011 Jul; 36(13):1755-62. doi:
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- Yoshiko Tsuboi, Takashi Doi, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda. Gallates of isoorientin and (2S)-1,2-propanediol glucoside from the leaves of Schoepfia jasminodora.
Journal of natural medicines.
2011 Jul; 65(3-4):617-22. doi:
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Journal of medical microbiology.
2011 Jun; 60(Pt 6):817-827. doi:
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Journal of veterinary science.
2011 Jun; 12(2):115-9. doi:
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Biomacromolecules.
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Chinese journal of integrative medicine.
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BMC biotechnology.
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