2-Furoic acid (BioDeep_00000002867)
Secondary id: BioDeep_00000405311, BioDeep_00000864035
human metabolite PANOMIX_OTCML-2023 Endogenous natural product
代谢物信息卡片
化学式: C5H4O3 (112.016)
中文名称: 2-糠酸, 糠酸
谱图信息:
最多检出来源 Homo sapiens(plant) 15.78%
Last reviewed on 2024-07-10.
Cite this Page
2-Furoic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/2-furoic_acid (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000002867). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C1=COC(=C1)C(=O)O
InChI: InChI=1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)
描述信息
Furoic acid is a metabolite that appears in the urine of workers occupationally exposed to furfural and is a marker of exposure to this compound. Furfural is a heterocyclic aldehyde that is commonly used as a solvent in industry. It is readily absorbed into the body via the lungs and has significant skin absorption. Furfural is an irritant of the eyes, mucous membranes, and skin and is a central nervous system depressant. Furfural as a confirmed animal carcinogen with unknown relevance to humans (It has been suggested that is a substance that produces hepatic cirrhosis). Once in the body, furfural is metabolized rapidly via oxidation to the metabolite furoic acid, which is then conjugated with glycine and excreted in the urine in both free and conjugated forms. (PMID: 3751566, 4630229, 12587683). 2-Furoic acid is a biomarker for the consumption of beer.
2-Furancarboxylic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=88-14-2 (retrieved 2024-07-10) (CAS RN: 88-14-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
2-Furoic acid (Furan-2-carboxylic acid) is an organic compound produced through furfural oxidation[1]. 2-Furoic acid exhibits hypolipidemic effet, lowers both serum cholesterol and serum triglyceride levels in rats[2].
2-Furoic acid (Furan-2-carboxylic acid) is an organic compound produced through furfural oxidation[1]. 2-Furoic acid exhibits hypolipidemic effet, lowers both serum cholesterol and serum triglyceride levels in rats[2].
2-Furoic acid (Furan-2-carboxylic acid) is an organic compound produced through furfural oxidation[1]. 2-Furoic acid exhibits hypolipidemic effet, lowers both serum cholesterol and serum triglyceride levels in rats[2].
同义名列表
44 个代谢物同义名
2-Furoic acid, sodium salt; alpha-Furancarboxylic acid; beta-Furancarboxylic acid; Furan-2-carboxylic acid; alpha-Furancarboxylate; Α-furancarboxylic acid; b-Furancarboxylic acid; 2-Furancarboxylic acid; a-Furancarboxylic acid; beta-Furancarboxylate; Furancarboxylic acid; Furan-2-carbonsaeure; Furan-2-carboxylate; Α-furancarboxylate; Furan-3-carboxylic; b-Furancarboxylate; 2-Furancarboxylate; a-Furancarboxylate; alpha-Furoic acid; Furan-2-ylacetate; beta-Furoic acid; Acide 2-furoique; Furancarboxylate; Acido 2-furoico; 2-Furanoic acid; Pyromucic acid; 2-Carboxyfuran; Α-furoic acid; a-Furoic acid; alpha-Furoate; 2-FUROIC ACID; b-Furoic acid; beta-Furoate; 2-Furanoate; furoic acid; Pyromucate; a-Furoate; Α-furoate; 2-Furoate; b-Furoate; Furoate; 2-Furoic acid; 2-Furoic acid; 2-Furoate
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:30845
- KEGG: C01546
- PubChem: 6919
- HMDB: HMDB0000617
- Metlin: METLIN2266
- ChEMBL: CHEMBL1232797
- Wikipedia: 2-Furoic_acid
- KNApSAcK: C00000151
- foodb: FDB000951
- chemspider: 10251740
- CAS: 88-14-2
- MoNA: KO000773
- MoNA: KO000771
- MoNA: KO000769
- MoNA: KO000772
- MoNA: KO000770
- PMhub: MS000006722
- ChEBI: CHEBI:16739
- PDB-CCD: FOA
- 3DMET: B00315
- NIKKAJI: J4.288I
- RefMet: 2-Furoic acid
- medchemexpress: HY-W012946
- PubChem: 4705
- KNApSAcK: 16739
- LOTUS: LTS0110632
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)
86 个相关的物种来源信息
- 25641 - Aloe: LTS0110632
- 1080010 - Aloe africana: 10.1021/JF071110T
- 1080010 - Aloe africana: LTS0110632
- 4454 - Araceae: LTS0110632
- 4890 - Ascomycota: LTS0110632
- 1131492 - Aspergillaceae: LTS0110632
- 5052 - Aspergillus: LTS0110632
- 1549217 - Aspergillus stellatus: 10.1016/S0031-9422(03)00189-4
- 1549217 - Aspergillus stellatus: LTS0110632
- 51383 - Asphodelaceae: LTS0110632
- 4381 - Campanulaceae: LTS0110632
- 29002 - Cercospora: LTS0110632
- 122368 - Cercospora beticola: 10.1080/00021369.1981.10864692
- 122368 - Cercospora beticola: LTS0110632
- 35718 - Chaetomiaceae: LTS0110632
- 5149 - Chaetomium: 10.1016/J.TETLET.2008.08.064
- 5149 - Chaetomium: LTS0110632
- 16399 - Codonopsis: LTS0110632
- 86864 - Codonopsis pilosula: 10.3390/MOLECULES23020383
- 86864 - Codonopsis pilosula: LTS0110632
- 86864 - Codonopsis pilosula Nannf.var.modesta(Nannf).L.Shen: -
- 5326 - Coriolus: -
- 16906 - Cornus Officinalis Sieb. Et Zucc.: -
- 767018 - Diaporthaceae: LTS0110632
- 147541 - Dothideomycetes: LTS0110632
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 2759 - Eukaryota: LTS0110632
- 147545 - Eurotiomycetes: LTS0110632
- 3803 - Fabaceae: LTS0110632
- 55182 - Forsythia: LTS0110632
- 205691 - Forsythia viridissima: 10.1155/2014/304830
- 205691 - Forsythia viridissima: LTS0110632
- 4751 - Fungi: LTS0110632
- 360145 - Grosmannia: LTS0110632
- 5161 - Grosmannia crassivaginata: 10.1016/0031-9422(94)00630-C
- 5161 - Grosmannia crassivaginata: LTS0110632
- 174172 - Homalomena: LTS0110632
- 714477 - Homalomena occulta: LTS0110632
- 714477 - Homalomena occulta: NA
- 9606 - Homo sapiens: -
- 4447 - Liliopsida: LTS0110632
- 3398 - Magnoliopsida: LTS0110632
- 39998 - Melastomataceae: LTS0110632
- 2212703 - Mucoromycetes: LTS0110632
- 1913637 - Mucoromycota: LTS0110632
- 93133 - Mycosphaerellaceae: LTS0110632
- 4144 - Oleaceae: LTS0110632
- 474995 - Ophiocordyceps: LTS0110632
- 72228 - Ophiocordyceps sinensis: 10.1021/NP100902F
- 72228 - Ophiocordyceps sinensis: LTS0110632
- 474942 - Ophiocordycipitaceae: LTS0110632
- 5152 - Ophiostomataceae: LTS0110632
- 40006 - Osbeckia: LTS0110632
- 113475 - Osbeckia chinensis: 10.1016/J.FITOTE.2014.01.007
- 113475 - Osbeckia chinensis: LTS0110632
- 3883 - Phaseolus: LTS0110632
- 3885 - Phaseolus vulgaris: 10.1246/BCSJ.60.981
- 3885 - Phaseolus vulgaris: LTS0110632
- 34399 - Phomopsis: LTS0110632
- 1807033 - Phomopsis velata: 10.1016/S0031-9422(00)83157-X
- 1807033 - Phomopsis velata: LTS0110632
- 4836 - Phycomyces: LTS0110632
- 4837 - Phycomyces blakesleeanus: 10.1016/0031-9422(96)00146-X
- 4837 - Phycomyces blakesleeanus: LTS0110632
- 1344966 - Phycomycetaceae: LTS0110632
- 189247 - Senecio scandens Buch.-Ham.: -
- 4070 - Solanaceae: LTS0110632
- 4107 - Solanum: LTS0110632
- 4081 - Solanum lycopersicum: 10.1038/SDATA.2014.29
- 4081 - Solanum lycopersicum: LTS0110632
- 147550 - Sordariomycetes: LTS0110632
- 132464 - Spatholobus: LTS0110632
- 455371 - Spatholobus suberectus: LTS0110632
- 455371 - Spatholobus suberectus: NA
- 35493 - Streptophyta: LTS0110632
- 166611 - Swertia angustifolia: -
- 58023 - Tracheophyta: LTS0110632
- 28568 - Trichocomaceae: LTS0110632
- 5117 - Valsaceae: LTS0110632
- 33090 - Viridiplantae: LTS0110632
- 3602 - Vitaceae: LTS0110632
- 3603 - Vitis: LTS0110632
- 29760 - Vitis vinifera:
- 29760 - Vitis vinifera: 10.1021/JF970894F
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 29760 - Vitis vinifera: LTS0110632
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
- Piyanard Boonnate, Ryusho Kariya, Paksiree Saranaruk, Ubon Cha'on, Kanlayanee Sawanyawisuth, Sarawut Jitrapakdee, Seiji Okada, Kulthida Vaeteewoottacharn. Five-(Tetradecyloxy)-2-furoic Acid Alleviates Cholangiocarcinoma Growth by Inhibition of Cell-cycle Progression and Induction of Apoptosis.
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JAMA network open.
2019 09; 2(9):e1911970. doi:
10.1001/jamanetworkopen.2019.11970
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Cardiovascular & hematological agents in medicinal chemistry.
2017 Nov; 15(1):40-48. doi:
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Phytopathology.
2014 Apr; 104(4):332-9. doi:
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Analytical and bioanalytical chemistry.
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