LS-775 (BioDeep_00000862795)

Main id: BioDeep_00000002332

 


代谢物信息卡片


InChI=1\C8H9NO2\c1-11-8(10)6-4-2-3-5-7(6)9\h2-5H,9H2,1H

化学式: C8H9NO2 (151.0633)
中文名称: 邻氨基苯甲酸甲酯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC(=O)C1=CC=CC=C1N
InChI: InChI=1S/C8H9NO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,9H2,1H3

描述信息

同义名列表

45 个代谢物同义名

InChI=1\C8H9NO2\c1-11-8(10)6-4-2-3-5-7(6)9\h2-5H,9H2,1H; Methylester kyseliny anthranilove [Czech]; Benzoic acid, 2-amino-, methyl ester; Epa Pesticide Chemical Code 128725; BENZOIC ACID METHYL ESTER,2-AMINO; 2-Aminobenzoic acid, methyl ester; o-Aminobenzoic acid, methyl ester; O-Aminobenzoic acid methyl ester; 2-Aminobenzoic acid methyl ester; Anthranilic acid, methyl ester; Anthranilic acid methyl ester; Methyl anthranilate (natural); Anthranilic acid methylester; 2-(Methoxycarbonyl)aniline; Amino methyl benzoate, o-; Methyl 2-aminobenzoate; Neroli oil, artificial; Methyl O-aminobenzoate; Neroli oil, artifical; O-Carbomethoxyaniline; 2-Carbomethoxyaniline; METHYL ANTHRANILATE; METHYLANTHRANILATE; EINECS 205-132-4; NCGC00091409-01; W268208_ALDRICH; W268216_ALDRICH; M29703_ALDRICH; 236454_ALDRICH; PS2055_SUPELCO; FEMA No. 2682; ZINC00157525; WLN: ZR BVO1; BRN 0606965; 10730_FLUKA; Nevoli oil; BB_SC-2799; CCRIS 1349; HSDB 1008; AI3-01022; 134-20-3; NSC 3109; NSC3109; LS-775; Methyl anthranilate



数据库引用编号

6 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)

14 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。

亚细胞结构定位 关联基因列表
Cytoplasm 7 AR, CCNL1, EIF2B1, RBFOX3, SNCA, TYR, TYRP1
Peripheral membrane protein 1 GORASP1
Endosome membrane 1 TYRP1
Endoplasmic reticulum membrane 1 DRD1
Nucleus 5 AR, CCNL1, DRD1, RBFOX3, SNCA
cytosol 4 ANK1, AR, EIF2B1, SNCA
nucleoplasm 4 AR, ATP2B1, CCNL1, MNT
Cell membrane 6 ATP2B1, DRD1, GRID1, OPRD1, TRPA1, TRPV1
Cytoplasmic side 1 GORASP1
Cell projection, axon 1 SNCA
Multi-pass membrane protein 7 ATP2B1, DRD1, GRID1, MPC1L, OPRD1, TRPA1, TRPV1
Golgi apparatus membrane 1 GORASP1
Synapse 2 ATP2B1, SNCA
cell cortex 1 SNCA
glutamatergic synapse 3 ATP2B1, DRD1, GRID1
Golgi apparatus 2 ATRN, GORASP1
Golgi membrane 2 GORASP1, INS
growth cone 1 SNCA
mitochondrial inner membrane 1 MPC1L
neuronal cell body 2 SNCA, TRPV1
postsynapse 1 SNCA
presynaptic membrane 3 ATP2B1, DRD1, OPRD1
sarcolemma 1 ANK1
Cytoplasm, cytosol 1 EIF2B1
Lysosome 2 SNCA, TYR
plasma membrane 12 ANK1, AR, ATP2B1, ATRN, BCHE, DRD1, EIF2B1, GRID1, OPRD1, SNCA, TRPA1, TRPV1
synaptic vesicle membrane 3 ATP2B1, OPRD1, SNCA
Membrane 8 ANK1, AR, ATP2B1, EIF2B1, OPRD1, SNCA, TRPA1, TRPV1
axon 1 SNCA
basolateral plasma membrane 2 ANK1, ATP2B1
extracellular exosome 3 ATP2B1, ATRN, GRID1
extracellular space 4 ATRN, BCHE, INS, SNCA
perinuclear region of cytoplasm 2 SNCA, TYR
mitochondrion 1 SNCA
protein-containing complex 2 AR, SNCA
intracellular membrane-bounded organelle 2 ATP2B1, TYR
Single-pass type I membrane protein 3 ATRN, TYR, TYRP1
Secreted 3 BCHE, INS, SNCA
extracellular region 3 BCHE, INS, SNCA
cytoplasmic side of plasma membrane 1 ANK1
[Isoform 2]: Secreted 1 ATRN
ciliary membrane 1 DRD1
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 TRPV1
actin cytoskeleton 1 SNCA
dendritic spine 1 DRD1
perikaryon 1 RBFOX3
Z disc 1 ANK1
Melanosome membrane 2 TYR, TYRP1
Golgi-associated vesicle 1 TYR
postsynaptic membrane 4 ANK1, DRD1, GRID1, TRPV1
Mitochondrion inner membrane 1 MPC1L
Cytoplasm, cytoskeleton 1 ANK1
axolemma 1 ANK1
GABA-ergic synapse 3 DRD1, GRID1, TRPV1
cis-Golgi network 1 GORASP1
intracellular vesicle 1 TYRP1
sarcoplasmic reticulum 1 ANK1
Cell projection, dendritic spine 1 DRD1
lateral plasma membrane 1 ATP2B1
nuclear speck 2 AR, CCNL1
Postsynaptic cell membrane 2 GRID1, TRPV1
Cell projection, neuron projection 1 TRPV1
neuron projection 2 ANK1, OPRD1
cilium 1 DRD1
chromatin 3 AR, CCNL1, MNT
stereocilium bundle 1 TRPA1
cell projection 1 ATP2B1
supramolecular fiber 1 SNCA
Chromosome 1 CCNL1
cytoskeleton 1 ANK1
chromosome, telomeric region 1 CCNL1
blood microparticle 1 BCHE
non-motile cilium 1 DRD1
Basolateral cell membrane 1 ATP2B1
[Isoform 3]: Secreted 1 ATRN
endosome lumen 1 INS
M band 1 ANK1
Nucleus, nucleoplasm 1 CCNL1
Cell projection, dendrite 1 DRD1
Melanosome 2 TYR, TYRP1
Nucleus speckle 1 CCNL1
Presynaptic cell membrane 1 ATP2B1
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 BCHE, INS
axon terminus 2 OPRD1, SNCA
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 2 GORASP1, INS
postsynaptic density membrane 2 GRID1, OPRD1
immunological synapse 1 ATP2B1
neuronal dense core vesicle 1 OPRD1
Golgi apparatus, cis-Golgi network membrane 1 GORASP1
nuclear envelope lumen 1 BCHE
clathrin-coated endocytic vesicle membrane 1 TYRP1
[Isoform 1]: Cell membrane 1 ATRN
dendrite membrane 1 OPRD1
nuclear origin of replication recognition complex 1 CCNL1
Cell projection, cilium membrane 1 DRD1
CMG complex 1 CCNL1
Cell projection, dendritic spine membrane 1 TRPV1
dendritic spine membrane 1 TRPV1
cyclin-dependent protein kinase holoenzyme complex 1 CCNL1
spectrin-associated cytoskeleton 1 ANK1
ankyrin-1 complex 1 ANK1
inclusion body 1 SNCA
photoreceptor ribbon synapse 1 ATP2B1
G protein-coupled receptor complex 1 DRD1
[Isoform Mu18]: Sarcoplasmic reticulum 1 ANK1
[Isoform Mu19]: Sarcoplasmic reticulum 1 ANK1
[Isoform Mu20]: Sarcoplasmic reticulum 1 ANK1
MCM complex 1 CCNL1
spine apparatus 1 OPRD1
eukaryotic translation initiation factor 2B complex 1 EIF2B1


文献列表

  • Vlad Dinu, Pallab Kumar Borah, Molly Muleya, David J Scott, Ryan Lithgo, Jacob Pattem, Stephen E Harding, Gleb E Yakubov, Ian D Fisk. Flavour compounds affect protein structure: The effect of methyl anthranilate on bovine serum albumin conformation. Food chemistry. 2022 Sep; 388(?):133013. doi: 10.1016/j.foodchem.2022.133013. [PMID: 35483284]
  • Jacob Pollier, Nathan De Geyter, Tessa Moses, Benoît Boachon, José M Franco-Zorrilla, Yuechen Bai, Elia Lacchini, Azra Gholami, Robin Vanden Bossche, Danièle Werck-Reichhart, Sofie Goormachtig, Alain Goossens. The MYB transcription factor Emission of Methyl Anthranilate 1 stimulates emission of methyl anthranilate from Medicago truncatula hairy roots. The Plant journal : for cell and molecular biology. 2019 08; 99(4):637-654. doi: 10.1111/tpj.14347. [PMID: 31009122]
  • Zi Wei Luo, Jae Sung Cho, Sang Yup Lee. Microbial production of methyl anthranilate, a grape flavor compound. Proceedings of the National Academy of Sciences of the United States of America. 2019 05; 116(22):10749-10756. doi: 10.1073/pnas.1903875116. [PMID: 31085637]
  • Jeremy Pillet, Alan H Chambers, Christopher Barbey, Zhilong Bao, Anne Plotto, Jinhe Bai, Michael Schwieterman, Timothy Johnson, Benjamin Harrison, Vance M Whitaker, Thomas A Colquhoun, Kevin M Folta. Identification of a methyltransferase catalyzing the final step of methyl anthranilate synthesis in cultivated strawberry. BMC plant biology. 2017 Aug; 17(1):147. doi: 10.1186/s12870-017-1088-1. [PMID: 28859633]
  • Bonnie J Ohler, Christelle Guédot, Richard S Zack, Peter J Landolt. Aggregation of Thaumatomyia glabra (Diptera: Chloropidae) Males on Iris spp. Flowers Releasing Methyl Anthranilate. Environmental entomology. 2016 12; 45(6):1476-1479. doi: 10.1093/ee/nvw140. [PMID: 28028094]
  • E J Bernklau, B E Hibbard, A P Norton, L B Bjostad. Methyl Anthranilate as a Repellent for Western Corn Rootworm Larvae (Coleoptera: Chrysomelidae). Journal of economic entomology. 2016 08; 109(4):1683-90. doi: 10.1093/jee/tow090. [PMID: 27122493]
  • Mariana Martins Gomes Pinheiro, Ana B Miltojević, Niko S Radulović, Ikarastika Rahayu Abdul-Wahab, Fabio Boylan, Patrícia Dias Fernandes. Anti-inflammatory activity of Choisya ternata Kunth essential oil, ternanthranin, and its two synthetic analogs (methyl and propyl N-methylanthranilates). PloS one. 2015; 10(3):e0121063. doi: 10.1371/journal.pone.0121063. [PMID: 25807367]
  • Alan H Chambers, Shane Alan Evans, Kevin M Folta. Methyl anthranilate and γ-decalactone inhibit strawberry pathogen growth and achene Germination. Journal of agricultural and food chemistry. 2013 Dec; 61(51):12625-33. doi: 10.1021/jf404255a. [PMID: 24328200]
  • Alexandra Esther, Ralf Tilcher, Jens Jacob. Assessing the effects of three potential chemical repellents to prevent bird damage to corn seeds and seedlings. Pest management science. 2013 Mar; 69(3):425-30. doi: 10.1002/ps.3288. [PMID: 22499556]
  • Rajinder S Mann, Jared G Ali, Sara L Hermann, Siddharth Tiwari, Kirsten S Pelz-Stelinski, Hans T Alborn, Lukasz L Stelinski. Induced release of a plant-defense volatile 'deceptively' attracts insect vectors to plants infected with a bacterial pathogen. PLoS pathogens. 2012; 8(3):e1002610. doi: 10.1371/journal.ppat.1002610. [PMID: 22457628]
  • Jiao Yin, Honglin Feng, Hongyan Sun, Jinghui Xi, Yazhong Cao, Kebin Li. Functional analysis of general odorant binding protein 2 from the meadow moth, Loxostege sticticalis L. (Lepidoptera: Pyralidae). PloS one. 2012; 7(3):e33589. doi: 10.1371/journal.pone.0033589. [PMID: 22479417]
  • David C Robacker, Michelle J Massa, Patrizia Sacchetti, Robert J Bartelt. A novel attractant for Anastrepha ludens (Diptera: Tephritidae) from a Concord grape product. Journal of economic entomology. 2011 Aug; 104(4):1195-203. doi: 10.1603/ec10220. [PMID: 21882683]
  • Daniela Roell, Thomas W Rösler, Stephanie Degen, Rudolf Matusch, Aria Baniahmad. Antiandrogenic activity of anthranilic acid ester derivatives as novel lead structures to inhibit prostate cancer cell proliferation. Chemical biology & drug design. 2011 Jun; 77(6):450-9. doi: 10.1111/j.1747-0285.2011.01116.x. [PMID: 21439024]
  • Christy E Manyi-Loh, Roland N Ndip, Anna M Clarke. Volatile compounds in honey: a review on their involvement in aroma, botanical origin determination and potential biomedical activities. International journal of molecular sciences. 2011; 12(12):9514-32. doi: 10.3390/ijms12129514. [PMID: 22272147]
  • Matthias Erb, Nicolas Foresti, Ted C J Turlings. A tritrophic signal that attracts parasitoids to host-damaged plants withstands disruption by non-host herbivores. BMC plant biology. 2010 Nov; 10(?):247. doi: 10.1186/1471-2229-10-247. [PMID: 21078181]
  • Tobias G Köllner, Claudia Lenk, Nan Zhao, Irmgard Seidl-Adams, Jonathan Gershenzon, Feng Chen, Jörg Degenhardt. Herbivore-induced SABATH methyltransferases of maize that methylate anthranilic acid using s-adenosyl-L-methionine. Plant physiology. 2010 Aug; 153(4):1795-807. doi: 10.1104/pp.110.158360. [PMID: 20519632]
  • Hayet Edziri, Maha Mastouri, Imed Cheraif, Mahjoub Aouni. Chemical composition and antibacterial, antifungal and antioxidant activities of the flower oil of Retama raetam (Forssk.) Webb from Tunisia. Natural product research. 2010 May; 24(9):789-96. doi: 10.1080/14786410802529190. [PMID: 20461625]
  • Frank Hippauf, Elke Michalsky, Ruiqi Huang, Robert Preissner, Todd J Barkman, Birgit Piechulla. Enzymatic, expression and structural divergences among carboxyl O-methyltransferases after gene duplication and speciation in Nicotiana. Plant molecular biology. 2010 Feb; 72(3):311-30. doi: 10.1007/s11103-009-9572-0. [PMID: 19936944]
  • Anna Wajs, Radoslaw Bonikowski, Danuta Kalemba. Different isolation methods for determination of composition of volatiles from Nigella damascena L. seeds. Natural product communications. 2009 Nov; 4(11):1577-80. doi: . [PMID: 19967995]
  • Jonas M Bengtsson, Yitbarek Wolde-Hawariat, Hamida Khbaish, Merid Negash, Bekele Jembere, Emiru Seyoum, Bill S Hansson, Mattias C Larsson, Ylva Hillbur. Field attractants for Pachnoda interrupta selected by means of GC-EAD and single sensillum screening. Journal of chemical ecology. 2009 Sep; 35(9):1063-76. doi: 10.1007/s10886-009-9684-7. [PMID: 19768509]
  • Fatima A Jabalpurwala, John M Smoot, Russell L Rouseff. A comparison of citrus blossom volatiles. Phytochemistry. 2009 Jul; 70(11-12):1428-34. doi: 10.1016/j.phytochem.2009.07.031. [PMID: 19747702]
  • Wipapan Pongcharoen, Vatcharin Rukachaisirikul, Masahiko Isaka, Kanlayanee Sriklung. Cytotoxic metabolites from the wood-decayed fungus Xylaria sp. BCC 9653. Chemical & pharmaceutical bulletin. 2007 Nov; 55(11):1647-8. doi: 10.1248/cpb.55.1647. [PMID: 17978529]
  • Jihong Wang, Vincenzo De Luca. The biosynthesis and regulation of biosynthesis of Concord grape fruit esters, including 'foxy' methylanthranilate. The Plant journal : for cell and molecular biology. 2005 Nov; 44(4):606-19. doi: 10.1111/j.1365-313x.2005.02552.x. [PMID: 16262710]
  • Eugene Sebastian J Nidiry, C S Bujji Babu. Antifungal activity of tuberose absolute and some of its constituents. Phytotherapy research : PTR. 2005 May; 19(5):447-9. doi: 10.1002/ptr.1630. [PMID: 16106389]
  • David G James. Further field evaluation of synthetic herbivore-induced plant volatiles as attractants for beneficial insects. Journal of chemical ecology. 2005 Mar; 31(3):481-95. doi: 10.1007/s10886-005-2020-y. [PMID: 15898496]
  • Leslie Hammack, Richard J Petroski. Field capture of northern and western corn rootworm beetles relative to attractant structure and volatility. Journal of chemical ecology. 2004 Sep; 30(9):1809-25. doi: 10.1023/b:joec.0000042403.88930.a7. [PMID: 15586676]
  • Louise Urruty, Jean-Luc Giraudel, Sovan Lek, Philippe Roudeillac, Michel Montury. Assessment of strawberry aroma through SPME/GC and ANN methods. Classification and discrimination of varieties. Journal of agricultural and food chemistry. 2002 May; 50(11):3129-36. doi: 10.1021/jf0116799. [PMID: 12009974]
  • Rafael del Campo, Julio J Criado, Eva García, María R Hermosa, A Jiménez-Sánchez, Juan L Manzano, Enrique Monte, E Rodríguez-Fernández, Francisca Sanz. Thiourea derivatives and their nickel(II) and platinum(II) complexes: antifungal activity. Journal of inorganic biochemistry. 2002 Apr; 89(1-2):74-82. doi: 10.1016/s0162-0134(01)00408-1. [PMID: 11931966]
  • S Moran. Aversion of the feral pigeon and the house sparrow to pellets and sprouts treated with commercial formulations of methyl anthranilate. Pest management science. 2001 Mar; 57(3):248-52. doi: 10.1002/ps.271. [PMID: 11455654]