85-91-6
85-91-6
Chemical Structure
Methyl N-methylanthranilate
- CAS. Nr.: 85-91-6
- Formula:C9H11NO2
- Molecular Weight:165.19
IUPAC Name: methyl 2-(methylamino)benzoate
InChIKey: GVOWHGSUZUUUDR-UHFFFAOYSA-N
SMILES: O=C(OC)C1=CC=CC=C1NC
Biological Activity: 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].
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Methyl N-methylanthranilate | 99.92% | 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. | ||||||||||||||||||||
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Methyl N-methylanthranilate (Standard) | ≥98% | Methyl N-methylanthranilate (Standard) is the analytical standard of Methyl N-methylanthranilate. This product is intended for research and analytical applications. 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. | ||||||||||||||||||||
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Methyl N-methylanthranilate-d3 | Methyl N-methylanthranilate-d3 is the deuterated-labeled Methyl N-methylanthranilate (HY-76705). Methyl N-methylanthranilate is an N-alkylated anthranilate with a sweet citrus aroma, which is commonly used in perfume manufacturing. Methyl N-methylanthranilate is the dominant component in the defensive secretion of the millipede Typhloiulus orpheus. Methyl N-methylanthranilate exhibits quorum sensing inhibition and anti-biofilm activity against P. aeruginosa; it interferes with PQS synthesis via competitive inhibition of PqsA, but lacks bactericidal activity. Methyl N-methylanthranilate is sensitive to UVA/sunlight in human skin cells, and generates O2•- through type I photodynamic reactions, leading to lysosomal/mitochondrial damage, double-strand DNA breaks and apoptosis, with potential phototoxicity. | |||||||||||||||||||||
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