Glucosamine (BioDeep_00000001863)
Secondary id: BioDeep_00000400233, BioDeep_00000412599
natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite Chemicals and Drugs Antibiotics BioNovoGene_Lab2019 Volatile Flavor Compounds
代谢物信息卡片
化学式: C6H13NO5 (179.0793688)
中文名称: 2-氨基-2-脱氧-D-吡喃葡萄糖, D-氨基葡萄糖, D-(+)-葡萄糖胺 盐酸盐, 氨基葡萄糖, β-D-葡糖胺, 葡糖胺
谱图信息:
最多检出来源 Homo sapiens(blood) 0.06%
分子结构信息
SMILES: C(C1C(C(C(C(O1)O)N)O)O)O
InChI: InChI=1/C6H13NO5/c7-3-5(10)4(9)2(1-8)12-6(3)11/h2-6,8-11H,1,7H2/t2-,3-,4-,5-,6u/m1/s1
描述信息
Glucosamine (C6H13NO5) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids. Glucosamine is part of the structure of two polysaccharides, chitosan and chitin. Glucosamine is one of the most abundant monosaccharides. Produced commercially by the hydrolysis of shellfish exoskeletons or, less commonly, by fermentation of a grain such as corn or wheat, glucosamine has many names depending on country. Although a common dietary supplement, there is little evidence that it is effective for relief of arthritis or pain, and is not an approved prescription drug. In the United States, glucosamine is not approved by the Food and Drug Administration for medical use in humans. Since glucosamine is classified as a dietary supplement, evidence of safety and efficacy is not required as long as it is not advertised as a treatment for a medical condition. Nevertheless, glucosamine is a popular alternative medicine used by consumers for the treatment of osteoarthritis. Glucosamine is also extensively used in veterinary medicine as an unregulated but widely accepted supplement. Treatment with oral glucosamine is commonly used for the treatment of osteoarthritis. Since glucosamine is a precursor for glycosaminoglycans, and glycosaminoglycans are a major component of joint cartilage, supplemental glucosamine may help to rebuild cartilage and treat arthritis. However, there is little evidence that any clinical effect of glucosamine works this way. Its use as a therapy for osteoarthritis appears safe but there is conflicting evidence as to its effectiveness. Glucosamine is naturally present in the shells of shellfish, animal bones, bone marrow, and fungi. D-Glucosamine is made naturally in the form of glucosamine-6-phosphate, and is the biochemical precursor of all nitrogen-containing sugars. Specifically in humans, glucosamine-6-phosphate is synthesized from fructose 6-phosphate and glutamine by glutamine—fructose-6-phosphate transaminase as the first step of the hexosamine biosynthesis pathway. The end-product of this pathway is uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), which is then used for making glycosaminoglycans, proteoglycans, and glycolipids. As the formation of glucosamine-6-phosphate is the first step for the synthesis of these products, glucosamine may be important in regulating their production; however, the way that the hexosamine biosynthesis pathway is actually regulated, and whether this could be involved in contributing to human disease remains unclear.
Present in mucopolysaccharides and in polysaccharides found in bacteria, fungi, higher plants, invertebrates, vertebrates, antibiotics and UDP complexes. Obt. comly. by hydrol. of seashells [CCD]
M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids
Acquisition and generation of the data is financially supported in part by CREST/JST.
KEIO_ID G051
Glucosamine (D-Glucosamine) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. Glucosamine also is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, which when administered exogenously, exerts pharmacological effects on osteoarthritic cartilage and chondrocytes[1].
Glucosamine (D-Glucosamine) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. Glucosamine also is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, which when administered exogenously, exerts pharmacological effects on osteoarthritic cartilage and chondrocytes[1].
Glucosamine (D-Glucosamine) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. Glucosamine also is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, which when administered exogenously, exerts pharmacological effects on osteoarthritic cartilage and chondrocytes[1].
同义名列表
28 个代谢物同义名
(3R,4R,5S,6R)-3-Amino-6-(hydroxymethyl)oxane-2,4,5-triol; Fides ecopharma brand OF glucosamine sulfate; Rottapharm brand OF glucosamine sulfate; Opfermann brand OF glucosamine sulfate; (+)-2-Amino-2-deoxy-D-glucopyranose; D-(+)-Glucosamine hydrochloride; 2-Amino-2-deoxy-D-glucopyranose; 2-Amino-2-deoxyhexopyranose; 2-Deoxy-2-amino-D-glucose; 2-Amino-2-deoxy-D-glucose; 2-Deoxy-2-aminoglucose; 2-Amino-2-deoxyglucose; 2 Amino 2 deoxyglucose; Sulfate, glucosamine; Glucosamine sulfate; D-(+)-Glucosamine; 2-Aminoglucose; D-Glucosamine; Hespercorbin; Glucosamine; Chitosamine; Cosamin; Dona S; Xicil; Dona; Glucosamine; D-Glucosamine; beta-D-Glucosamine
数据库引用编号
39 个数据库交叉引用编号
- ChEBI: CHEBI:47977
- ChEBI: CHEBI:17315
- ChEBI: CHEBI:5417
- KEGG: C00329
- KEGGdrug: D04334
- PubChem: 439213
- PubChem: 739
- HMDB: HMDB0001514
- Metlin: METLIN63216
- DrugBank: DB01296
- ChEMBL: CHEMBL493287
- Wikipedia: Glucosamine
- MeSH: Glucosamine
- KNApSAcK: C00001121
- foodb: FDB022668
- chemspider: 388352
- CAS: 3416-24-8
- CAS: 90-77-7
- MoNA: KO002995
- MoNA: KO002997
- MoNA: PR100125
- MoNA: KO002994
- MoNA: KO002996
- MoNA: KO002998
- MoNA: PS019901
- MoNA: PR100126
- PMhub: MS000001320
- PubChem: 3623
- PDB-CCD: GCS
- PDB-CCD: PA1
- 3DMET: B04670
- NIKKAJI: J10.582A
- RefMet: Glucosamine
- medchemexpress: HY-B1125
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-120
- KNApSAcK: 47977
- LOTUS: LTS0168935
- LOTUS: LTS0095471
- LOTUS: LTS0192727
分类词条
相关代谢途径
BioCyc(8)
PlantCyc(0)
代谢反应
67 个相关的代谢反应过程信息。
Reactome(33)
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHIT + H2O ⟶ ADGP
- Digestion and absorption:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion of dietary carbohydrate:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
CHIT + H2O ⟶ ADGP
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion and absorption:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion of dietary carbohydrate:
H2O + limit dextrin ⟶ Glc + Mal + maltotriose
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion and absorption:
H2O + phosphate monoester ⟶ Alcohol + Pi
- Digestion:
H2O + phosphate monoester ⟶ Alcohol + Pi
- Digestion of dietary carbohydrate:
CHIT + H2O ⟶ ADGP
- Digestion and absorption:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion:
CHEST + H2O ⟶ CHOL + LCFAs
- Digestion of dietary carbohydrate:
H2O ⟶ Mal + maltotriose
- Digestion and absorption:
CHIT + H2O ⟶ ADGP
BioCyc(15)
- chitin degradation I (archaea):
β-D-glucosaminyl-(1→4)-N-acetyl-D-glucosamine + H2O ⟶ N-acetyl-D-glucosamine + D-glucosamine
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitin derivatives degradation:
N,N'-diacetylchitobiose + phosphate ⟶ N-acetyl-α-D-glucosamine 1-phosphate + N-acetyl-D-glucosamine
- heparan sulfate degradation:
N-sulfo-D-glucosamine + H2O ⟶ D-glucosamine + sulfate
- heparin degradation:
N-sulfo-D-glucosamine + H2O ⟶ D-glucosamine + sulfate
- chitobiose degradation:
N-monoacetylchitobiose 6'-phosphate + H2O ⟶ N-acetyl-D-glucosamine 6-phosphate + D-glucosamine
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitin derivatives degradation:
D-glucosamine 6-phosphate + H2O ⟶ D-fructose-6-phosphate + H+ + ammonia
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitobiose degradation:
N-monoacetylchitobiose 6'-phosphate + H2O ⟶ N-acetyl-D-glucosamine 6-phosphate + D-glucosamine
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
- chitobiose degradation:
N,N'-diacetylchitobiose 6'-phosphate + H2O ⟶ N-monoacetylchitobiose 6'-phosphate + acetate
WikiPathways(0)
Plant Reactome(0)
INOH(1)
- Aminosugars metabolism ( Aminosugars metabolism ):
D-Fructose 6-phosphate + NH3 ⟶ D-Glucosamine 6-phosphate + H2O
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(18)
- Amino Sugar Metabolism:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Sialuria or French Type Sialuria:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Salla Disease/Infantile Sialic Acid Storage Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Amino Sugar Metabolism:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Sialuria or French Type Sialuria:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Salla Disease/Infantile Sialic Acid Storage Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Chitobiose Degradation:
Diacetylchitobiose-6-phosphate + Water ⟶ Acetic acid + N'-monoacetylchitobiose-6'-phosphate
- Amino Sugar Metabolism:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Amino Sugar Metabolism:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Amino Sugar Metabolism:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Sialuria or French Type Sialuria:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Salla Disease/Infantile Sialic Acid Storage Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
PharmGKB(0)
57 个相关的物种来源信息
- 6656 - Arthropoda: LTS0095471
- 4890 - Ascomycota: LTS0095471
- 2 - Bacteria: LTS0095471
- 2 - Bacteria: LTS0168935
- 2 - Bacteria: LTS0192727
- 6658 - Branchiopoda: LTS0095471
- 3481 - Cannabaceae: LTS0095471
- 3482 - Cannabis: LTS0095471
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 3483 - Cannabis sativa: LTS0095471
- 7711 - Chordata: LTS0095471
- 6668 - Daphnia: LTS0095471
- 6669 - Daphnia pulex: 10.1038/SREP25125
- 6669 - Daphnia pulex: LTS0095471
- 77658 - Daphniidae: LTS0095471
- 543 - Enterobacteriaceae: LTS0095471
- 561 - Escherichia: LTS0095471
- 562 - Escherichia coli: LTS0095471
- 33682 - Euglenozoa: LTS0095471
- 2759 - Eukaryota: LTS0095471
- 4751 - Fungi: LTS0095471
- 1236 - Gammaproteobacteria: LTS0095471
- 9606 - Homo sapiens: -
- 14101 - Juncaceae: LTS0095471
- 13578 - Juncus: LTS0095471
- 879918 - Juncus roemerianus: 10.18785/GRR.0602.07
- 879918 - Juncus roemerianus: LTS0095471
- 5653 - Kinetoplastea: LTS0095471
- 147547 - Lecanoromycetes: LTS0095471
- 4447 - Liliopsida: LTS0095471
- 3398 - Magnoliopsida: LTS0095471
- 40674 - Mammalia: LTS0095471
- 33208 - Metazoa: LTS0095471
- 10066 - Muridae: LTS0095471
- 10088 - Mus: LTS0095471
- 10090 - Mus musculus: LTS0095471
- 10090 - Mus musculus: NA
- 1762 - Mycobacteriaceae: LTS0168935
- 1762 - Mycobacteriaceae: LTS0192727
- 1763 - Mycobacterium: LTS0168935
- 1763 - Mycobacterium: LTS0192727
- 1769 - Mycobacterium leprae: LTS0168935
- 1769 - Mycobacterium leprae: LTS0192727
- 1773 - Mycobacterium tuberculosis: LTS0168935
- 1773 - Mycobacterium tuberculosis: LTS0192727
- 56479 - Ramalina: LTS0095471
- 157169 - Ramalina fraxinea: 10.5586/ASBP.1979.002
- 157169 - Ramalina fraxinea: LTS0095471
- 56478 - Ramalinaceae: LTS0095471
- 35493 - Streptophyta: LTS0095471
- 58023 - Tracheophyta: LTS0095471
- 5690 - Trypanosoma: LTS0095471
- 5691 - Trypanosoma brucei: 10.1371/JOURNAL.PNTD.0001618
- 5691 - Trypanosoma brucei: LTS0095471
- 5654 - Trypanosomatidae: LTS0095471
- 33090 - Viridiplantae: LTS0095471
- 569774 - 金线莲: -
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
- Yuan Zhang, Line A Borch, Niklas H Fischer, Morten Meldal. Hydrodynamic Control of Alzheimer Aβ Fibrillation with Glucosaminic Acid Containing Click-Cyclized β-Bodies.
Journal of the American Chemical Society.
2024 Jan; 146(4):2654-2662. doi:
10.1021/jacs.3c12118
. [PMID: 38126710] - Mazlyzam Abdul Latif, Asrul Mustafa, Lee Chee Keong, Asmah Hamid. Chromolaena odorata layered-nitrile rubber polymer transdermal patch enhanced wound healing in vivo.
PloS one.
2024; 19(3):e0295381. doi:
10.1371/journal.pone.0295381
. [PMID: 38466676] - Sang-Min Kim, Dong Yeol Kim, Jiwon Park, Young-Ah Moon, Inn-Oc Han. Glucosamine increases macrophage lipid accumulation by regulating the mammalian target of rapamycin signaling pathway.
BMB reports.
2023 Nov; ?(?):. doi:
. [PMID: 37964636]
- Akshayaa Venkataraghavan, Julian G Schwerdt, Stephen D Tyerman, Maria Hrmova. Barley Nodulin 26-like Intrinsic Protein permeates water, metalloids, saccharides, and ion pairs due to structural plasticity and diversification.
The Journal of biological chemistry.
2023 Oct; ?(?):105410. doi:
10.1016/j.jbc.2023.105410
. [PMID: 37913906] - Yi Zou, Zongkai Liu, Wenjia Liu, Zhaidong Liu. Current knowledge and potential intervention of hexosamine biosynthesis pathway in lung cancer.
World journal of surgical oncology.
2023 Oct; 21(1):334. doi:
10.1186/s12957-023-03226-z
. [PMID: 37880766] - Feng Li, Zhengyan Zhang, Yan Bai, Qishi Che, Hua Cao, Jiao Guo, Zhengquan Su. Glucosamine Improves Non-Alcoholic Fatty Liver Disease Induced by High-Fat and High-Sugar Diet through Regulating Intestinal Barrier Function, Liver Inflammation, and Lipid Metabolism.
Molecules (Basel, Switzerland).
2023 Oct; 28(19):. doi:
10.3390/molecules28196918
. [PMID: 37836761] - Yihao Liu, Zhen Qin, Chunling Wang, Zhengqiang Jiang. N-acetyl-d-glucosamine-based oligosaccharides from chitin: Enzymatic production, characterization and biological activities.
Carbohydrate polymers.
2023 Sep; 315(?):121019. doi:
10.1016/j.carbpol.2023.121019
. [PMID: 37230627] - Zeqi Li, Bo Fu, Aili Wei, Yanchen Wu, Ming Huang, Enhao Zhang, Bo Cui, Bo Wang, Hui Peng. d-Glucosamine induces circadian phase delay by promoting BMAL1 degradation through AMPK/mTOR pathway.
Life sciences.
2023 Jul; 325(?):121765. doi:
10.1016/j.lfs.2023.121765
. [PMID: 37169147] - Giorgia Della Rocca, Carlo Schievano, Alessandra Di Salvo, Maria Beatrice Conti, Maria Federica Della Valle. Palmitoyl-glucosamine co-micronized with curcumin for maintenance of meloxicam-induced pain relief in dogs with osteoarthritis pain.
BMC veterinary research.
2023 Feb; 19(1):37. doi:
10.1186/s12917-023-03594-4
. [PMID: 36747264] - Yingde Xu, Liangjie Sun, Xiaodan Gao, Jingkuan Wang. Contrasting response of fungal versus bacterial residue accumulation within soil aggregates to long-term fertilization.
Scientific reports.
2022 10; 12(1):17834. doi:
10.1038/s41598-022-22064-9
. [PMID: 36284223] - G Zhou, M W Zhao, Y P Cao, J H Lin, W G Wang, A Guo, H Tian. [A multicenter cross-sectional study of quality of life and nonsurgical treatment in patients with knee osteoarthritis].
Zhonghua yi xue za zhi.
2022 Sep; 102(35):2799-2805. doi:
10.3760/cma.j.cn112137-20220406-00719
. [PMID: 36124353] - Ying Chen, Xiaoming Liao, Pei Jing, Liangkui Hu, Zengqiu Yang, Yongchao Yao, Chunyan Liao, Shiyong Zhang. Linoleic Acid-Glucosamine Hybrid for Endogenous Iron-Activated Ferroptosis Therapy in High-Grade Serous Ovarian Cancer.
Molecular pharmaceutics.
2022 09; 19(9):3187-3198. doi:
10.1021/acs.molpharmaceut.2c00333
. [PMID: 35939328] - Kun Gao, Yukun Qin, Linsong Wang, Xin Li, Song Liu, Ronge Xing, HuaHua Yu, Xiaolin Chen, Pengcheng Li. Design, Synthesis, and Antifungal Activities of Hymexazol Glycosides Based on a Biomimetic Strategy.
Journal of agricultural and food chemistry.
2022 Aug; 70(30):9520-9535. doi:
10.1021/acs.jafc.2c02507
. [PMID: 35877994] - Jing Chen, Li-Na Huo, Yuan Gao, Yun-Li Zhang, Ye Chen. Two new N-acetyl-ᴅ-glucosamine derivatives from the medical algae-derived endophytic fungus Penicillium chrysogenum.
Natural product research.
2022 Aug; 36(15):3988-3991. doi:
10.1080/14786419.2021.1889543
. [PMID: 33957817] - Venkanna Babu Mullapudi, Kendall C Craig, Zhongwu Guo. Design and Synthesis of a Doubly Functionalized Core Structure of a Glycosylphosphatidylinositol Anchor Containing Photoreactive and Clickable Functional Groups.
The Journal of organic chemistry.
2022 07; 87(14):9419-9425. doi:
10.1021/acs.joc.2c00901
. [PMID: 35766889] - Bojian Chen, Lei Fang, Liangzhuo Lin, Yang Lv, Zexin Huang, Xiaodong Lin, Xin Wang. Aerobic exercise combined with glucosamine hydrochloride capsules inhibited the apoptosis of chondrocytes in rabbit knee osteoarthritis by affecting TRPV5 expression.
Gene.
2022 Jul; 830(?):146465. doi:
10.1016/j.gene.2022.146465
. [PMID: 35427733] - Alexandre de Fátima Cobre, Monica Surek, Dile Pontarolo Stremel, Mariana Millan Fachi, Helena Hiemisch Lobo Borba, Fernanda Stumpf Tonin, Roberto Pontarolo. Diagnosis and prognosis of COVID-19 employing analysis of patients' plasma and serum via LC-MS and machine learning.
Computers in biology and medicine.
2022 Jul; 146(?):105659. doi:
10.1016/j.compbiomed.2022.105659
. [PMID: 35751188] - Yanmin Gao, Yanli Ma, Di Xie, Hua Jiang. ManNAc protects against podocyte pyroptosis via inhibiting mitochondrial damage and ROS/NLRP3 signaling pathway in diabetic kidney injury model.
International immunopharmacology.
2022 Jun; 107(?):108711. doi:
10.1016/j.intimp.2022.108711
. [PMID: 35338958] - Janeala J Morsby, Bradley D Smith. Advances in Optical Sensors of N-Acetyl-β-d-hexosaminidase (N-Acetyl-β-d-glucosaminidase).
Bioconjugate chemistry.
2022 04; 33(4):544-554. doi:
10.1021/acs.bioconjchem.2c00057
. [PMID: 35302753] - Peipei Han, Yingying Wei, Shu Jiang, Yi Chen, Feng Xu, Hongfei Wang, Xingfeng Shao. N-Acetyl-d-glucosamine Inhibition of Hexokinase Results in Downregulation of the Phenylpropanoid Metabolic Pathway and Decreased Resistance to Brown Rot in Peach Fruit.
Journal of agricultural and food chemistry.
2022 Mar; 70(12):3917-3928. doi:
10.1021/acs.jafc.1c06573
. [PMID: 35298175] - Salim Cerig, Fatime Geyikoglu. Oxidative stress and cyto-genotoxicity induced by poly-d-glucosamine in human blood cells in vitro.
Zeitschrift fur Naturforschung. C, Journal of biosciences.
2022 Jan; 77(1-2):43-55. doi:
10.1515/znc-2021-0080
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EMBO molecular medicine.
2022 01; 14(1):e15389. doi:
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Frontiers in immunology.
2022; 13(?):926304. doi:
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Genetics in medicine : official journal of the American College of Medical Genetics.
2021 11; 23(11):2067-2075. doi:
10.1038/s41436-021-01259-x
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Microbiological research.
2021 Oct; 251(?):126830. doi:
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Cell death & disease.
2021 09; 12(10):889. doi:
10.1038/s41419-021-04164-y
. [PMID: 34588426] - Laura Morelli, Luigi Lay, Darielys Santana-Mederos, Yury Valdes-Balbin, Vicente Verez Bencomo, Angela van Diepen, Cornelis H Hokke, Fabrizio Chiodo, Federica Compostella. Glycan Array Evaluation of Synthetic Epitopes between the Capsular Polysaccharides from Streptococcus pneumoniae 19F and 19A.
ACS chemical biology.
2021 09; 16(9):1671-1679. doi:
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Journal of medicinal chemistry.
2021 08; 64(16):12261-12272. doi:
10.1021/acs.jmedchem.1c00896
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International journal of molecular sciences.
2021 Aug; 22(17):. doi:
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Molecules (Basel, Switzerland).
2021 Jul; 26(14):. doi:
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Nutrients.
2021 Jun; 13(7):. doi:
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Life sciences.
2021 Jun; 275(?):119375. doi:
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Current biology : CB.
2021 06; 31(11):2374-2385.e4. doi:
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Rejuvenation research.
2021 Jun; 24(3):220-226. doi:
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Drugs in R&D.
2021 Jun; 21(2):189-202. doi:
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Comparative medicine.
2021 06; 71(3):215-221. doi:
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Pakistan journal of pharmaceutical sciences.
2021 May; 34(3(Special)):1277-1282. doi:
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Drug metabolism and personalized therapy.
2021 04; 36(4):259-270. doi:
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Rheumatology (Oxford, England).
2021 03; 60(3):1205-1209. doi:
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Journal of musculoskeletal & neuronal interactions.
2021 03; 21(1):113-120. doi:
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Toxicology and applied pharmacology.
2021 02; 412(?):115371. doi:
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Biomaterials.
2021 02; 269(?):120631. doi:
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Wiadomosci lekarskie (Warsaw, Poland : 1960).
2021; 74(8):1975-1983. doi:
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The Journal of biological chemistry.
2021 Jan; 296(?):100624. doi:
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Computational and mathematical methods in medicine.
2021; 2021(?):5499450. doi:
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Frontiers in endocrinology.
2021; 12(?):627745. doi:
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PloS one.
2021; 16(5):e0252279. doi:
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Biochemistry.
2020 12; 59(48):4581-4590. doi:
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Molecules (Basel, Switzerland).
2020 Dec; 25(24):. doi:
10.3390/molecules25245782
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Journal of enzyme inhibition and medicinal chemistry.
2020 Dec; 35(1):1879-1890. doi:
10.1080/14756366.2020.1826941
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Chronobiology international.
2020 11; 37(11):1528-1537. doi:
10.1080/07420528.2020.1784189
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Journal of medicinal chemistry.
2020 10; 63(20):11691-11706. doi:
10.1021/acs.jmedchem.0c00851
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Journal of alternative and complementary medicine (New York, N.Y.).
2020 Oct; 26(10):945-955. doi:
10.1089/acm.2020.0128
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Biochimica et biophysica acta. Molecular and cell biology of lipids.
2020 10; 1865(10):158764. doi:
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Kidney360.
2020 09; 1(9):957-961. doi:
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Applied biochemistry and biotechnology.
2020 Sep; 192(1):230-242. doi:
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Nutrients.
2020 Aug; 12(9):. doi:
10.3390/nu12092661
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The journal of physical chemistry letters.
2020 Aug; 11(16):6655-6663. doi:
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Biomolecules.
2020 08; 10(8):. doi:
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Clinical therapeutics.
2020 08; 42(8):e140-e149. doi:
10.1016/j.clinthera.2020.06.009
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Drug development and industrial pharmacy.
2020 Aug; 46(8):1265-1277. doi:
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Complementary therapies in medicine.
2020 May; 50(?):102349. doi:
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Journal of orthopaedic surgery and research.
2020 Apr; 15(1):150. doi:
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Carbohydrate polymers.
2020 Apr; 233(?):115856. doi:
10.1016/j.carbpol.2020.115856
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Food chemistry.
2020 Feb; 306(?):125613. doi:
10.1016/j.foodchem.2019.125613
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The American journal of the medical sciences.
2020 02; 359(2):79-83. doi:
10.1016/j.amjms.2019.12.013
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Journal of medicinal food.
2020 Feb; 23(2):139-146. doi:
10.1089/jmf.2019.0022
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Archives of toxicology.
2020 02; 94(2):449-467. doi:
10.1007/s00204-019-02642-z
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Journal of pharmaceutical and biomedical analysis.
2020 Jan; 178(?):112954. doi:
10.1016/j.jpba.2019.112954
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Journal of the American Chemical Society.
2020 01; 142(4):1975-1986. doi:
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Frontiers in endocrinology.
2020; 11(?):514. doi:
10.3389/fendo.2020.00514
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International journal of nanomedicine.
2020; 15(?):2921-2933. doi:
10.2147/ijn.s247443
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Anti-inflammatory & anti-allergy agents in medicinal chemistry.
2020; 19(2):190-201. doi:
10.2174/1871523018666190115094512
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Arthritis research & therapy.
2019 11; 21(1):254. doi:
10.1186/s13075-019-2048-y
. [PMID: 31779692] - Da Eun Lee, Su Jin Lee, Su Ji Kim, Hyun-Shik Lee, Oh-Shin Kwon. Curcumin Ameliorates Nonalcoholic Fatty Liver Disease through Inhibition of O-GlcNAcylation.
Nutrients.
2019 Nov; 11(11):. doi:
10.3390/nu11112702
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Advances in therapy.
2019 11; 36(11):3221-3237. doi:
10.1007/s12325-019-01064-8
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Applied microbiology and biotechnology.
2019 Oct; 103(19):7883-7889. doi:
10.1007/s00253-019-10084-x
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Glycobiology.
2019 09; 29(10):705-714. doi:
10.1093/glycob/cwz049
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Journal of the American Society for Mass Spectrometry.
2019 Sep; 30(9):1679-1689. doi:
10.1007/s13361-019-02233-3
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Chemical research in toxicology.
2019 08; 32(8):1572-1582. doi:
10.1021/acs.chemrestox.9b00097
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Food & function.
2019 Aug; 10(8):5008-5017. doi:
10.1039/c9fo00981g
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Free radical biology & medicine.
2019 08; 139(?):55-69. doi:
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International journal of biological macromolecules.
2019 Jul; 132(?):795-800. doi:
10.1016/j.ijbiomac.2019.03.234
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Aging clinical and experimental research.
2019 Jun; 31(6):807-813. doi:
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Scientific reports.
2019 05; 9(1):7496. doi:
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Molecular pharmacology.
2019 05; 95(5):475-489. doi:
10.1124/mol.118.114199
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Cellular and molecular biology (Noisy-le-Grand, France).
2019 Mar; 65(3):76-83. doi:
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- Chun-Man Huang, Syue-Yi Lyu, Kuan-Hung Lin, Chun-Liang Chen, Mei-Hua Chen, Hao-Wei Shih, Ning-Shian Hsu, I-Wen Lo, Yung-Lin Wang, Yi-Shan Li, Chang-Jer Wu, Tsung-Lin Li. Teicoplanin Reprogrammed with the N-Acyl-Glucosamine Pharmacophore at the Penultimate Residue of Aglycone Acquires Broad-Spectrum Antimicrobial Activities Effectively Killing Gram-Positive and -Negative Pathogens.
ACS infectious diseases.
2019 03; 5(3):430-442. doi:
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Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2019 Mar; 125(?):95-105. doi:
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