3-Hydroxybenzoicacid (BioDeep_00000265120)
Main id: BioDeep_00000001248
PANOMIX_OTCML-2023 BioNovoGene_Lab2019 natural product
代谢物信息卡片
化学式: C7H6O3 (138.03169259999999)
中文名称: 3-羟基苯甲酸, 间羟基苯甲酸
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CC(=CC(=C1)O)C(=O)O
InChI: InChI=1S/C7H6O3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H,(H,9,10)
描述信息
A monohydroxybenzoic acid that is benzoic acid substituted by a hydroxy group at position 3. It has been isolated from Taxus baccata. It is used as an intermediate in the synthesis of plasticisers, resins, pharmaceuticals, etc.
3-Hydroxybenzoic acid is an endogenous metabolite.
3-Hydroxybenzoic acid is an endogenous metabolite.
同义名列表
数据库引用编号
18 个数据库交叉引用编号
- ChEBI: CHEBI:30764
- KEGG: C00587
- PubChem: 7420
- ChEMBL: CHEMBL65369
- KNApSAcK: C00048480
- CAS: 25302-76-5
- CAS: 99-06-9
- MetaboLights: MTBLC30764
- ChEBI: CHEBI:16193
- PubChem: 3866
- KNApSAcK: C00040822
- PDB-CCD: 3HB
- 3DMET: B00140
- NIKKAJI: J43.202D
- medchemexpress: HY-W004049
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-508
- KNApSAcK: 16193
- LOTUS: LTS0176105
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)
76 个相关的物种来源信息
- 654 - Aeromonas veronii: 10.3389/FCIMB.2020.00044
- 155619 - Agaricomycetes: LTS0176105
- 287749 - Alysicarpus: LTS0176105
- 1766240 - Alysicarpus monilifer: 10.1080/10575630290034258
- 1766240 - Alysicarpus monilifer: LTS0176105
- 4210 - Asteraceae: LTS0176105
- 5204 - Basidiomycota: LTS0176105
- 3504 - Betula: LTS0176105
- 3505 - Betula pendula: 10.1007/BF00575727
- 3505 - Betula pendula: LTS0176105
- 3514 - Betulaceae: LTS0176105
- 21019 - Castanea: LTS0176105
- 21020 - Castanea sativa: 10.1016/S0031-9422(00)86043-4
- 21020 - Castanea sativa: LTS0176105
- 5250 - Ceratobasidiaceae: LTS0176105
- 4345 - Ericaceae: LTS0176105
- 2759 - Eukaryota: LTS0176105
- 3803 - Fabaceae: LTS0176105
- 3503 - Fagaceae: LTS0176105
- 23170 - Filipendula: LTS0176105
- 57917 - Filipendula ulmaria: 10.1515/ZNC-2001-9-1012
- 57917 - Filipendula ulmaria: LTS0176105
- 200992 - Fumaria: LTS0176105
- 200993 - Fumaria officinalis: 10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
- 200993 - Fumaria officinalis: LTS0176105
- 367484 - Fumaria vaillantii: 10.1002/(SICI)1099-1565(199901/02)10:1<6::AID-PCA431>3.0.CO;2-0
- 367484 - Fumaria vaillantii: LTS0176105
- 4751 - Fungi: LTS0176105
- 49747 - Gladiolus: 10.1515/ZNC-1996-7-814
- 49747 - Gladiolus: LTS0176105
- 20685 - Indigofera: LTS0176105
- 198899 - Indigofera oblongifolia: 10.1007/BF02977339
- 198899 - Indigofera oblongifolia: LTS0176105
- 26339 - Iridaceae: LTS0176105
- 4136 - Lamiaceae: LTS0176105
- 4447 - Liliopsida: LTS0176105
- 3869 - Lupinus: LTS0176105
- 3871 - Lupinus angustifolius: 10.1007/BF00993699
- 3871 - Lupinus angustifolius: LTS0176105
- 3398 - Magnoliopsida: LTS0176105
- 13625 - Paeonia: LTS0176105
- 40708 - Paeonia emodi: 10.1080/1057563021000060103
- 40708 - Paeonia emodi: LTS0176105
- 24943 - Paeoniaceae: LTS0176105
- 3465 - Papaveraceae: LTS0176105
- 4479 - Poaceae: LTS0176105
- 4274 - Polygalaceae: LTS0176105
- 362626 - Rhaponticum: LTS0176105
- 362630 - Rhaponticum carthamoides: 10.1016/J.PHYTOCHEM.2009.04.008
- 456999 - Rhizoctonia solani: 10.1038/200575A0
- 456999 - Rhizoctonia solani: LTS0176105
- 3745 - Rosaceae: LTS0176105
- 21880 - Salvia: LTS0176105
- 342065 - Salvia trijuga: 10.1076/PHBI.41.5.375.15938
- 342065 - Salvia trijuga: LTS0176105
- 4277 - Securidaca: LTS0176105
- 690845 - Securidaca longipedunculata: 10.1002/JMS.314
- 35493 - Streptophyta: LTS0176105
- 5238 - Thanatephorus: LTS0176105
- 107832 - Thanatephorus cucumeris: 10.1038/200575A0
- 107832 - Thanatephorus cucumeris: LTS0176105
- 58023 - Tracheophyta: LTS0176105
- 13730 - Tragopogon: LTS0176105
- 261649 - Tragopogon orientalis: 10.5586/ASBP.1988.009
- 261649 - Tragopogon orientalis: LTS0176105
- 41653 - Tragopogon pratensis: 10.5586/ASBP.1988.009
- 41653 - Tragopogon pratensis: LTS0176105
- 13749 - Vaccinium: LTS0176105
- 13750 - Vaccinium macrocarpon: 10.1021/JF020055F
- 13750 - Vaccinium macrocarpon: LTS0176105
- 180763 - Vaccinium myrtillus: 10.1111/J.1365-2621.1987.TB14056.X
- 180763 - Vaccinium myrtillus: LTS0176105
- 33090 - Viridiplantae: LTS0176105
- 4575 - Zea: LTS0176105
- 4577 - Zea mays: 10.1021/JF020957G
- 4577 - Zea mays: LTS0176105
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
- Xue-Qiang Cao, Xing-Yu Ouyang, Bo Chen, Kai Song, Lian Zhou, Bo-Le Jiang, Ji-Liang Tang, Guanghai Ji, Alan R Poplawsky, Ya-Wen He. Genetic Interference Analysis Reveals that Both 3-Hydroxybenzoic Acid and 4-Hydroxybenzoic Acid Are Involved in Xanthomonadin Biosynthesis in the Phytopathogen Xanthomonas campestris pv. campestris.
Phytopathology.
2020 Feb; 110(2):278-286. doi:
10.1094/phyto-08-19-0299-r
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Protein and peptide letters.
2020; 27(3):187-192. doi:
10.2174/0929866526666191002142301
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Nutrition research (New York, N.Y.).
2017 Oct; 46(?):88-95. doi:
10.1016/j.nutres.2017.09.006
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Chemosphere.
2017 Jul; 179(?):290-297. doi:
10.1016/j.chemosphere.2017.03.103
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Natural product research.
2016 Aug; 30(16):1880-4. doi:
10.1080/14786419.2015.1081196
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The Journal of nutritional biochemistry.
2016 07; 33(?):111-8. doi:
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The Journal of nutritional biochemistry.
2015 Nov; 26(11):1379-84. doi:
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2015 Jan; 15(?):10. doi:
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2014 Jan; 42(2):882-92. doi:
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Molecular plant-microbe interactions : MPMI.
2013 Oct; 26(10):1239-48. doi:
10.1094/mpmi-04-13-0112-r
. [PMID: 23718125] - Stefania Montersino, Roberto Orru, Arjan Barendregt, Adrie H Westphal, Esther van Duijn, Andrea Mattevi, Willem J H van Berkel. Crystal structure of 3-hydroxybenzoate 6-hydroxylase uncovers lipid-assisted flavoprotein strategy for regioselective aromatic hydroxylation.
The Journal of biological chemistry.
2013 Sep; 288(36):26235-26245. doi:
10.1074/jbc.m113.479303
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Phytochemical analysis : PCA.
2012 Nov; 23(6):588-97. doi:
10.1002/pca.2359
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Molecular microbiology.
2011 Sep; 81(5):1374-89. doi:
10.1111/j.1365-2958.2011.07772.x
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Molecular plant-microbe interactions : MPMI.
2011 Aug; 24(8):948-57. doi:
10.1094/mpmi-02-11-0031
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BMC plant biology.
2011 Apr; 11(?):66. doi:
10.1186/1471-2229-11-66
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2011 Apr; 36(7):922-5. doi:
10.4268/cjcmm20110722
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Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2010 Nov; 35(21):2852-61. doi:
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Journal of experimental botany.
2010 Oct; 61(15):4325-38. doi:
10.1093/jxb/erq234
. [PMID: 20729481] - Kennan Kellaris Salinero, Keith Keller, William S Feil, Helene Feil, Stephan Trong, Genevieve Di Bartolo, Alla Lapidus. Metabolic analysis of the soil microbe Dechloromonas aromatica str. RCB: indications of a surprisingly complex life-style and cryptic anaerobic pathways for aromatic degradation.
BMC genomics.
2009 Aug; 10(?):351. doi:
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2008 Oct; 33(19):2204-6. doi:
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Bioorganic & medicinal chemistry.
2008 Apr; 16(8):4589-93. doi:
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. [PMID: 18314336] - Zhen Xie, Zhong-Lin Zhang, Shane Hanzlik, Everett Cook, Qingxi J Shen. Salicylic acid inhibits gibberellin-induced alpha-amylase expression and seed germination via a pathway involving an abscisic-acid-inducible WRKY gene.
Plant molecular biology.
2007 Jun; 64(3):293-303. doi:
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. [PMID: 17390108] - Chao-Bin Xue, Li Zhang, Wan-Chun Luo, Xian-Ye Xie, Lin Jiang, Ting Xiao. 3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.
Bioorganic & medicinal chemistry.
2007 Mar; 15(5):2006-15. doi:
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Analytical and bioanalytical chemistry.
2004 Jan; 378(2):536-43. doi:
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