methyl N-methylanthranilate (CHEBI:142267)

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ChEBI Name	methyl N-methylanthranilate

ChEBI ID	CHEBI:142267

ChEBI ASCII Name	methyl N-methylanthranilate

Definition	A methyl ester resulting from the formal condensation of the carboxy group of N-methylanthranilic acid with methanol.

Stars	This entity has been manually annotated by the ChEBI Team.

Submitter	Mark Williams

Supplier Information

Download	Molfile XML SDF

Formula

C9H11NO2

Net Charge

Average Mass

165.189

Monoisotopic Mass

165.07898

InChI

InChI=1S/C9H11NO2/c1-10-8-6-4-3-5-7(8)9(11)12-2/h3-6,10H,1-2H3

InChIKey

GVOWHGSUZUUUDR-UHFFFAOYSA-N

SMILES

CNC1=CC=CC=C1C(OC)=O

Metabolite of Species	Details
Zanthoxylum beecheyanum (NCBI:txid1056465)	Found in stem (BTO:0001300). See: Cheng, M.J., Wu, C.C., Tsai, I.L. and Chen, I.S. (2004) Chemical and antiplatelet constituents from the stem of Zanthoxylum beecheyanum. J. Chin. Chem. Soc., 51(5A), 1065-1072.
Typhloiulus orpheus (NCBI:txid1522048)	Found in whole organism (UBERON:0000468). See: PubMed
Monascus sp. (NCBI:txid1963841)	See: Cheng, M.J., Wu, M.D., Chen, I.S. and Yuan, G.F. (2011). Chemical constituents isolated from the fungus Monascus sp. Chem. Nat. Compd., 47(4), 566-570.
Citrus x paradisi (NCBI:txid37656)	See: PubMed
Murraya paniculata (NCBI:txid43711)	Found in bark (BTO:0001301). Isolated from root bark See: Imai, F., Itoh, K., Kishibuchi, N., Kinoshita, T. and Sankawa, U. (1989) Constituents of the root bark of Murraya paniculata collected in Indonesia. Chem. Pharm. Bull., 37(1), 119-123.
Citrus unshiu (NCBI:txid55188)	See: Kekelidze, N.A. and Dzhanikashvili, M.I. (1985) The essential oils of the fruits of early-ripening varieties of Citrus unshiu. Chem. Nat. Compd., 21(4), 540-541.
Citrus reticulata (NCBI:txid85571)	Found in leaf (BTO:0000713). See: PubMed

Roles Classification
Chemical Role(s):	Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound )

Biological Role(s):	fungal metabolite Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds. plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. animal metabolite Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.

ChEBI Ontology
Outgoing	methyl N-methylanthranilate (CHEBI:142267) has functional parent N-methylanthranilic acid (CHEBI:16394) methyl N-methylanthranilate (CHEBI:142267) has role animal metabolite (CHEBI:75767) methyl N-methylanthranilate (CHEBI:142267) has role fungal metabolite (CHEBI:76946) methyl N-methylanthranilate (CHEBI:142267) has role plant metabolite (CHEBI:76924) methyl N-methylanthranilate (CHEBI:142267) is a benzoate ester (CHEBI:36054) methyl N-methylanthranilate (CHEBI:142267) is a methyl ester (CHEBI:25248) methyl N-methylanthranilate (CHEBI:142267) is a secondary amino compound (CHEBI:50995) methyl N-methylanthranilate (CHEBI:142267) is a substituted aniline (CHEBI:48975)

IUPAC Name

methyl 2-(methylamino)benzoate

Synonyms	Sources
2-methylaminobenzoic acid methyl ester	HMDB
2-methylaminomethyl benzoate	NIST Chemistry WebBook
dimethyl anthranilate	HMDB
methyl methanthranilate	HMDB
methyl methylaminobenzoate	HMDB
methyl methylanthranilate	HMDB
methyl N-methyl anthranylate	ChEBI
N-methylanthranilic acid, methyl ester	HMDB

Last Modified

28 September 2018