4-Methoxybenzaldehyde (BioDeep_00000230960)

 

Secondary id: BioDeep_00000002900, BioDeep_00000397451, BioDeep_00000861769

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


p-Anisaldehyde, United States Pharmacopeia (USP) Reference Standard

化学式: C8H8O2 (136.0524268)
中文名称: 4-甲氧基苯甲醛, 对甲氧基苯甲醛, 茴香醛, 对甲氧基苯甲醛
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 2.56%

分子结构信息

SMILES: COC1=CC=C(C=C1)C=O
InChI: InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

描述信息

4-Methoxybenzaldehyde, also known as 4-anisaldehyde or p-formylanisole, belongs to the class of organic compounds known as benzoyl derivatives, with the chemical formula CH3OC6H4CHO. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-). Anisaldehyde is prepared commercially by oxidation of 4-methoxytoluene (p-cresyl methyl ether) using manganese dioxide to convert a methyl group to the aldehyde group. 4-Methoxybenzaldehyde is a sweet, almond, and anise tasting compound. 4-Methoxybenzaldehyde can be found, on average, in the highest concentration within a few different foods, such as cumins, star anises, and fennels. 4-Methoxybenzaldehyde has also been detected, but not quantified, in several different foods, such as cornmints, anises, herbs and spices, tarragons, and tea. The related ortho isomer has a scent of licorice. It is a colorless liquid with a strong aroma. A solution of para-anisaldehyde in acid and ethanol is a useful stain in thin layer chromatography. Different chemical compounds on the plate can give different colors, allowing easy distinction. It is used as an intermediate in the synthesis of other compounds important in pharmaceuticals and perfumery.
P-methoxybenzaldehyde is a member of the class of benzaldehydes consisting of benzaldehyde itself carrying a methoxy substituent at position 4. It has a role as an insect repellent, a human urinary metabolite, a plant metabolite and a bacterial metabolite.
4-Methoxybenzaldehyde is a natural product found in Vanilla pompona, Solidago odora, and other organisms with data available.
See also: Anise Oil (part of).
Found in anise oil, fennel and vanilla. Flavouring ingredient
4-Methoxybenzaldehyde is a naturally occurring fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking [1].
4-Methoxybenzaldehyde is a naturally occurring fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking [1].

同义名列表

69 个代谢物同义名

p-Anisaldehyde, United States Pharmacopeia (USP) Reference Standard; p-Anisaldehyde, certified reference material, TraceCERT(R); p-Anisaldehyde, primary pharmaceutical reference standard; InChI=1/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H; 4-08-00-00252 (Beilstein Handbook Reference); MEPYRAMINE MALEATE IMPURITY P [EP IMPURITY]; MEPYRAMINE MALEATE IMPURITY P (EP IMPURITY); 4-anisaldehyde, 1,2,3,4,5,6-(14)C6-labeled; p-Anisaldehyde, for synthesis, 98.0\\%; 4-anisaldehyde, formyl-(14)C-labeled; p-Anisaldehyde, analytical standard; p-Anisaldehyde,p-Methoxybenzaldhyde; BENZALDEHYDE,4-METHOXY MFC8 H8 O2; p-Anisaldehyde, natural, 98\\%, FG; p-Anisaldehyde, >=97.5\\%, FCC, FG; 4-methoxybenzene carboxaldehyde; p-Methoxybenzylidenemalonitrile; p-Methoxybenzaldehyde (natural); P-METHOXYBENZALDEHYDE [FHFI]; 4-anisaldehyde, 18O-labeled; P-METHOXYBENZALDEHYDE [FCC]; p-Methoxybenzaldehyde-13C6; para-methoxy benzaldehyde; PARA- METHOXYBENZALDEHYDE; 4-(methyloxy)benzaldehyde; para-methoxybenzaldehyde; Benzaldehyde, 4-methoxy-; benzaldehyde, 4-methoxy; 4-methoxybenzylaldehyde; P-ANISALDEHYDE (USP-RS); P-ANISALDEHYDE [USP-RS]; p-Anisaldehyde, Reagent; p-methoxy benzaldehyde; 4-Methoxy-benzaldehyde; 4-methoxy benzaldehyde; 4-methoxylbenzaldehyde; 4-methoxybenzaldehyde; P-ANISALDEHYDE [HSDB]; p-methoxybenzaldehyde; 4-methoxybezaldehyde; p-Anisaldehyde, 98\\%; 4-methoxybenzaldehye; Anisaldehyde (para); p-Anisaldehyde, 8CI; P-ANISALDEHYDE [MI]; ANISALDEHYDE [INCI]; P-Anisaldehyde,(S); para-anisaldehyde; p-Anisic aldehyde; Formylanisole, p-; Anisic aldehyde; p-Formylanisole; UNII-9PA5V6656V; 4-anisaldehyde; p-Anisaldehyde; Anis aldehyde; WLN: VHR DO1; anisaldehyde; Tox21_201943; Tox21_303331; anisaldehyd; 9PA5V6656V; AI3-00223; FEMA 2670; Crategine; Aubepine; Anisic; Obepin; anisal



数据库引用编号

19 个数据库交叉引用编号

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)

47 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

  • Shanshan Shen, Jixin Zhang, Haoran Sun, Zhongqi Zu, Jialin Fu, Ranqin Fan, Qi Chen, Yu Wang, Pengxiang Yue, Jingming Ning, Liang Zhang, Xueling Gao. Sensomics-Assisted Characterization of Fungal-Flowery Aroma Components in Fermented Tea Using Eurotium cristatum. Journal of agricultural and food chemistry. 2023 Nov; ?(?):. doi: 10.1021/acs.jafc.3c05273. [PMID: 37962281]
  • Katherine R Tucker, Cassandra H Steele, Emily G McDermott. Aedes aegypti (L.) and Anopheles stephensi Liston (Diptera: Culicidae) Susceptibility and Response to Different Experimental Formulations of a Sodium Ascorbate Toxic Sugar Bait. Journal of medical entomology. 2022 09; 59(5):1710-1720. doi: 10.1093/jme/tjac101. [PMID: 35861727]
  • Raimondas Mozūraitis, David Hall, Nina Trandem, Baiba Ralle, Kalle Tunström, Lene Sigsgaard, Catherine Baroffio, Michelle Fountain, Jerry Cross, Atle Wibe, Anna-Karin Borg-Karlson. Composition of Strawberry Floral Volatiles and their Effects on Behavior of Strawberry Blossom Weevil, Anthonomus rubi. Journal of chemical ecology. 2020 Dec; 46(11-12):1069-1081. doi: 10.1007/s10886-020-01221-2. [PMID: 33030638]
  • Gunda Thöming, Sándor Koczor, Ferenc Szentkirályi, Hans R Norli, Marco Tasin, Geir K Knudsen. Attraction of Chrysotropia ciliata (Neuroptera, Chrysopidae) Males to P-Anisaldehyde, a Compound with Presumed Pheromone Function. Journal of chemical ecology. 2020 Jul; 46(7):597-609. doi: 10.1007/s10886-020-01191-5. [PMID: 32588285]
  • Yetunde Adewunmi, Sanchirmaa Namjilsuren, William D Walker, Dahlia N Amato, Douglas V Amato, Olga V Mavrodi, Derek L Patton, Dmitri V Mavrodi. Antimicrobial Activity of, and Cellular Pathways Targeted by, p-Anisaldehyde and Epigallocatechin Gallate in the Opportunistic Human Pathogen Pseudomonas aeruginosa. Applied and environmental microbiology. 2020 02; 86(4):. doi: 10.1128/aem.02482-19. [PMID: 31811038]
  • Ehab Mahran, Ibrahim El Gamal, Michael Keusgen, Gertrud E Morlock. Effect-directed analysis by high-performance thin-layer chromatography for bioactive metabolites tracking in Primula veris flower and Primula boveana leaf extracts. Journal of chromatography. A. 2019 Nov; 1605(?):460371. doi: 10.1016/j.chroma.2019.460371. [PMID: 31375330]
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  • Jinxin Che, Xiumei Chen, Qiuli Ouyang, Nengguo Tao. p-Anisaldehyde Exerts Its Antifungal Activity Against Penicillium digitatum and Penicillium italicum by Disrupting the Cell Wall Integrity and Membrane Permeability. Journal of microbiology and biotechnology. 2019 Jun; 30(6):878-884. doi: 10.4014/jmb.1911.11032. [PMID: 32160698]
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  • Dongfei Han, Ji-Young Ryu, Robert A Kanaly, Hor-Gil Hur. Isolation of a gene responsible for the oxidation of trans-anethole to para-anisaldehyde by Pseudomonas putida JYR-1 and its expression in Escherichia coli. Applied and environmental microbiology. 2012 Aug; 78(15):5238-46. doi: 10.1128/aem.00781-12. [PMID: 22610435]
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  • Michael Paul, Gerit Brüning, Jochen Bergmann, Johann Jauch. A thin-layer chromatography method for the identification of three different olibanum resins (Boswellia serrata, Boswellia papyrifera and Boswellia carterii, respectively, Boswellia sacra). Phytochemical analysis : PCA. 2012 Mar; 23(2):184-9. doi: 10.1002/pca.1341. [PMID: 21858880]
  • Cibele Bonacorsi, Maria Stella G Raddi, Luiz Marcos da Fonseca, Miriam Sannomiya, Wagner Vilegas. Effect of Byrsonima crassa and phenolic constituents on Helicobacter pylori-induced neutrophils oxidative burst. International journal of molecular sciences. 2012; 13(1):133-41. doi: 10.3390/ijms13010133. [PMID: 22312243]
  • Eun-Young Jeong, Kyoung-Shik Cho, Hoi-Seon Lee. Food protective effects of Periploca sepium oil and its active component against stored food mites. Journal of food protection. 2012 Jan; 75(1):118-22. doi: 10.4315/0362-028x.jfp-11-315. [PMID: 22221363]
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  • Li Liu, Hongyue Ma, Yuping Tang, Wenxing Chen, Yin Lu, Jianming Guo, Jin-Ao Duan. Discovery of estrogen receptor α modulators from natural compounds in Si-Wu-Tang series decoctions using estrogen-responsive MCF-7 breast cancer cells. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(1):154-63. doi: 10.1016/j.bmcl.2011.11.041. [PMID: 22137340]
  • Muthu Kumaradoss Mohan Maruga Raja, Shri Hari Mishra. Isolation, characterization and thin-layer chromatography method development of clerosterol palmityl ester: a chemical marker for standardization of leaves of Clerodendrum phlomidis. Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine. 2012 Jan; 10(1):109-13. doi: 10.3736/jcim20120116. [PMID: 22237282]
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  • Sheikh Shreaz, Rimple Bhatia, Neelofar Khan, Sumathi Muralidhar, Seemi F Basir, Nikhat Manzoor, Luqman Ahmad Khan. Exposure of Candida to p-anisaldehyde inhibits its growth and ergosterol biosynthesis. The Journal of general and applied microbiology. 2011; 57(3):129-36. doi: 10.2323/jgam.57.129. [PMID: 21817824]
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