3187-58-4
Chemical Structure
Methyl orsellinate
- CAS No.: 3187-58-4
- Formula:C9H10O4
- Molecular Weight:182.17
IUPAC Name: methyl 2,4-dihydroxy-6-methylbenzoate
InChIKey: NCCWCZLEACWJIN-UHFFFAOYSA-N
SMILES: COC(C1=C(C=C(O)C=C1O)C)=O
Biological Activity: Methyl orsellinate acts as an antiviral agent and insecticide. Methyl orsellinate exhibits enzyme inhibitory activity, with an IC50 of 59.6 µM against porcine leukocyte 5-lipoxygenase (5-LOX); it inhibits soybean 15-lipoxygenase (15-LOX), and shows weak inhibitory activity against acetylcholinesterase (AChE) and glutathione S-transferase (GST). Methyl orsellinate displays contact toxicity against adult Drosophila suzukii. Methyl orsellinate shows anti-HSV-1 activity. Methyl orsellinate can be used in studies related to *Drosophila suzukii* infestation and HSV-1 infection[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Methyl orsellinate | 99.91% | Methyl orsellinate acts as an antiviral agent and insecticide. Methyl orsellinate exhibits enzyme inhibitory activity, with an IC50 of 59.6 µM against porcine leukocyte 5-lipoxygenase (5-LOX); it inhibits soybean 15-lipoxygenase (15-LOX), and shows weak inhibitory activity against acetylcholinesterase (AChE) and glutathione S-transferase (GST). Methyl orsellinate displays contact toxicity against adult Drosophila suzukii. Methyl orsellinate shows anti-HSV-1 activity. Methyl orsellinate can be used in studies related to *Drosophila suzukii* infestation and HSV-1 infection. | ||||||||||||||||||||
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- [1]. Kim J, et al. Insecticidal and Enzyme Inhibitory Activities of Sparassol and Its Analogues against Drosophila suzukii. Journal of agricultural and food chemistry. 2016 Jul 13;64(27):5479-83. [Content Brief]
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[2]. Bhat NB, et al. Molecular docking and dynamics supported investigation of antiviral activity of Lichen metabolites of Roccella montagnei: an in silico and in vitro study. J Biomol Struct Dyn. 2023;41(21):11484-11497.
[Content Brief] - [3]. Ingólfsdóttir K, et al. Effects of tenuiorin and methyl orsellinate from the lichen Peltigera leucophlebia on 5-/15-lipoxygenases and proliferation of malignant cell lines in vitro. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2002 Oct;9(7):654-8. [Content Brief]
Keywords