85-91-6 (BioDeep_00000862735)
Main id: BioDeep_00000017467
PANOMIX_OTCML-2023
Metabolite Card
Formula: C9H11NO2 (165.079)
Chinese Names: 2-(甲氨基)苯甲酸甲酯, N-甲基邻氨基苯甲酸甲酯
Spectrum Hits:
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Molecular Structure
SMILES: CNC1=CC=CC=C1C(=O)OC
InChI: InChI=1S/C9H11NO2/c1-10-8-6-4-3-5-7(8)9(11)12-2/h3-6,10H,1-2H3
Description
Methyl N-methylanthranilate, a terpene, is a pungent compound that can be found in Citrus reticulate Blanco leaves. Methyl N-methylanthranilate has the potential for pain research[1].
Methyl N-methylanthranilate, a terpene, is a pungent compound that can be found in Citrus reticulate Blanco leaves. Methyl N-methylanthranilate has the potential for pain research[1].
Synonyms
38 synonym names
BENZOIC ACID METHYL ESTER,2-METHYLAMINO (N-METHYL-ANTHRANILIC ACID METHYL ESTER); InChI=1\C9H11NO2\c1-10-8-6-4-3-5-7(8)9(11)12-2\h3-6,10H,1-2H; Benzoic acid, 2-(methylamino)-, methyl ester; 4-14-00-01016 (Beilstein Handbook Reference); Anthranilic acid, N-methyl-, methyl ester; N-Methylanthranilic acid, methyl ester; 2-Methylaminobenzoic acid methyl ester; Dimethyl anthranilate (natural); Methyl N-methyl-o-anthranilate; Methyl o-(methylamino)benzoate; Methyl 2-(methylamino)benzoate; N-Methyl methyl anthranilate; 2-Methylaminomethyl benzoate; Methyl 2-methylaminobenzoate; Methyl-N-methylanthranilate; Methyl N-methylanthranilate; Methyl methylaminobenzoate; Methyl methylanthranilate; Methyl methanthranilate; Dimethyl anthranilate; EINECS 201-642-6; W271802_ALDRICH; W271810_ALDRICH; WLN: 1OVR BM1; FEMA No. 2718; ZINC00157414; SMR000112458; MLS000515990; BRN 0607217; 65820_FLUKA; CCRIS 2846; HSDB 2784; AI3-03340; ST5407122; NSC 9406; 85-91-6; NSC9406; Methyl 2-(methylamino)benzoate
Cross Reference
5 cross reference id
- ChEBI: CHEBI:142267
- PubChem: 6826
- ChEMBL: CHEMBL1409791
- CAS: 85-91-6
- medchemexpress: HY-76705
Classification Terms
Related Pathways
Reactome(0)
BioCyc(0)
PlantCyc(0)
Biological Process
0 related biological process reactions.
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
13 organism taxonomy source information
- 3708 - Brassica napus: 10.3389/FNUT.2022.822033
- 558547 - Citrus deliciosa:
- 37334 - Citrus maxima: 10.1021/JF051373S
- 85571 - Citrus reticulata:
- 85571 - Citrus Reticulata: -
- 55188 - Citrus unshiu:
- 3039 - Euglena gracilis: 10.3389/FBIOE.2021.662655
- 3847 - Glycine max: 10.1002/PMIC.201700366
- 43711 - Murraya paniculata: 10.1248/CPB.37.119
- 33090 - Plants: -
- 1056465 - Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
- 354523 - 吴茱萸: -
- 33090 - 陈皮: -
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。
Literature Reference
- Ana B Miltojević, Nikola M Stojanović, Pavle J Randjelović, Niko S Radulović. Distribution of methyl and isopropyl N-methylanthranilates and their metabolites in organs of rats treated with these two essential-oil constituents.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2019 Jun; 128(?):68-80. doi:
10.1016/j.fct.2019.03.039
. [PMID: 30914356] - Niko S Radulović, Ana B Miltojević, Nikola M Stojanović, Pavle J Randjelović. Distinct urinary metabolite profiles of two pharmacologically active N-methylanthranilates: Three approaches to xenobiotic metabolite identification.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2017 Nov; 109(Pt 1):341-355. doi:
10.1016/j.fct.2017.09.006
. [PMID: 28888736] - Edwin Correa, Winston Quiñones, Fernando Echeverri. Methyl-N-methylanthranilate, a pungent compound from Citrus reticulata Blanco leaves.
Pharmaceutical biology.
2016; 54(4):569-71. doi:
10.3109/13880209.2015.1044618
. [PMID: 26471095] - Mariana Martins Gomes Pinheiro, Niko S Radulović, Ana B Miltojević, Fabio Boylan, Patrícia Dias Fernandes. Antinociceptive esters of N-methylanthranilic acid: Mechanism of action in heat-mediated pain.
European journal of pharmacology.
2014 Mar; 727(?):106-14. doi:
10.1016/j.ejphar.2013.12.042
. [PMID: 24486396] - Niko S Radulović, Ana B Miltojević, Pavle J Randjelović, Nikola M Stojanović, Fabio Boylan. Effects of methyl and isopropyl N-methylanthranilates from Choisya ternata Kunth (Rutaceae) on experimental anxiety and depression in mice.
Phytotherapy research : PTR.
2013 Sep; 27(9):1334-8. doi:
10.1002/ptr.4877
. [PMID: 23132808] - Mun Wai Cheong, Zhi Soon Chong, Shao Quan Liu, Weibiao Zhou, Philip Curran, Bin Yu. Characterisation of calamansi (Citrus microcarpa). Part I: volatiles, aromatic profiles and phenolic acids in the peel.
Food chemistry.
2012 Sep; 134(2):686-95. doi:
10.1016/j.foodchem.2012.02.162
. [PMID: 23107679] - Niko S Radulović, Ana B Miltojević, Michael McDermott, Steve Waldren, John Adrian Parnell, Mariana Martins Gomes Pinheiro, Patricia Dias Fernandes, Fabio de Sousa Menezes. Identification of a new antinociceptive alkaloid isopropyl N-methylanthranilate from the essential oil of Choisya ternata Kunth.
Journal of ethnopharmacology.
2011 Jun; 135(3):610-9. doi:
10.1016/j.jep.2011.03.035
. [PMID: 21420481] - C B Detoni, E C M Cabral-Albuquerque, S V A Hohlemweger, C Sampaio, T F Barros, E S Velozo. Essential oil from Zanthoxylum tingoassuiba loaded into multilamellar liposomes useful as antimicrobial agents.
Journal of microencapsulation.
2009 Dec; 26(8):684-91. doi:
10.1080/02652040802661887
. [PMID: 19888877] - Anne-Laure Gancel, Patrick Ollitrault, Yann Froelicher, Felix Tomi, Camille Jacquemond, Francois Luro, Jean-Marc Brillouet. Leaf volatile compounds of seven citrus somatic tetraploid hybrids sharing willow leaf mandarin (Citrus deliciosa Ten.) as their common parent.
Journal of agricultural and food chemistry.
2003 Sep; 51(20):6006-13. doi:
10.1021/jf0345090
. [PMID: 13129309] - D M Musher, D P Griffith, G B Templeton. Further observations on the potentiation of the antibacterial effect of methenamine by acetohydroxamic acid.
The Journal of infectious diseases.
1976 May; 133(5):564-7. doi:
10.1093/infdis/133.5.564
. [PMID: 4573]