Spiromesifen Metabolite M01
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| Category | Others |
| Catalog number | BBF-04566 |
| CAS | 148476-30-6 |
| Molecular Weight | 272.34 |
| Molecular Formula | C17H20O3 |
| Purity | ≥90% |
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Description
It is the metabolite of Spiromesifen, which is a spirocyclic tetronic acid, environmentally friendly and novel structural pesticide.
Specification
| Synonyms | 1-Oxaspiro[4.4]non-3-en-2-one, 4-hydroxy-3-(2,4,6-trimethylphenyl)-; 3-Mesityl-2-oxo-1-oxaspiro(4.4)non-3-en-4-ol; Spiromesifen-alcohol; 4-Hydroxy-3-mesityl-1-oxaspiro(4.4)non-3-en-2-one |
| Storage | Store at -20°C under inert atmosphere |
| IUPAC Name | 4-hydroxy-3-(2,4,6-trimethylphenyl)-1-oxaspiro[4.4]non-3-en-2-one |
| Canonical SMILES | CC1=CC(=C(C(=C1)C)C2=C(C3(CCCC3)OC2=O)O)C |
| InChI | InChI=1S/C17H20O3/c1-10-8-11(2)13(12(3)9-10)14-15(18)17(20-16(14)19)6-4-5-7-17/h8-9,18H,4-7H2,1-3H3 |
| InChI Key | UWNPKBJDSGDYAU-UHFFFAOYSA-N |
Properties
| Appearance | White to Off-white Solid |
| Boiling Point | 478.9±45.0°C (Predicted) |
| Melting Point | >190°C (dec.) |
| Density | 1.20±0.1 g/cm3 (Predicted) |
| Solubility | Slightly soluble in DMSO, Methanol |
Reference Reading
1. Assessing the bioavailability and biotoxicity of spiromesifen and its main metabolite spiromesifen-enol (M01) reveals the defense mechanisms of earthworms (Eisenia fetida)
Tong Liu, Binning Wang, Jianwei Fang, Saihong Yan, Xiuguo Wang, Kuan Fang Sci Total Environ . 2022 Mar 20;813:151910. doi: 10.1016/j.scitotenv.2021.151910.
As a promising acaricide and potentially hazardous material, the defense mechanisms of non-target organisms to its exposure are unknown. This study investigates the bioavailability and biotoxicity of spiromesifen and spiromesifen-enol (M01), its main metabolite, in Eisenia fetida. The results showed that M01 was more persistent in the soil environment and E. fetida than spiromesifen. Transcriptome analysis indicated that the spiromesifen- and M01-induced differentially expressed genes (DEGs) were mainly enriched in lysosomal and phagosomal pathways. Analysis of the key common DEGs showed that both spiromesifen and M01 significantly influenced the lysosomes, phagosomes, antioxidant systems, and detoxification systems. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that spiromesifen and M01 damaged E. fetida epidermis and enhanced lysosomal and phagosomal activities. Significant oxidative stress effects were observed at the end of exposure. The hydroxyl free radical (·OH-) content and neutral red retention time (NRRT) could serve as sensitive early biomarkers to predict their pollution. These results revealed the synergistic effects of the epidermis, lysosomes, phagosomes, antioxidant systems, and detoxification system in resisting spiromesifen- and M01-induced damage, which could contribute to the defense mechanisms of non-target organisms against these pollutants.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
