71283-80-2
Chemical Structure
Fenoxaprop-P-ethyl
- CAS No.: 71283-80-2
- Formula:C18H16ClNO5
- Molecular Weight:361.78
IUPAC Name: ethyl (R)-2-(4-((6-chlorobenzo[d]oxazol-2-yl)oxy)phenoxy)propanoate
InChIKey: PQKBPHSEKWERTG-LLVKDONJSA-N
SMILES: C[C@@H](OC1=CC=C(OC2=NC3=CC=C(Cl)C=C3O2)C=C1)C(OCC)=O
Biological Activity: Fenoxaprop-P-ethyl is an acetyl-CoA carboxylase (ACC) inhibitor and post-emergence herbicide. Fenoxaprop-P-ethyl inhibits the conversion of acetyl-CoA to malonyl-CoA, reduces malonyl-CoA synthesis and disrupts fatty acid synthesis. Fenoxaprop-P-ethyl disrupts lipid homeostasis through cascaded inhibition of lipid metabolism, decreases total lipid content, downregulates fatty acid elongase genes and inhibits their activity. Fenoxaprop-P-ethyl disrupts fatty acid synthesis in rice seedlings and controls annual monocotyledonous weeds in wheat, durum wheat, rye, triticale and barley fields[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fenoxaprop-P-ethyl | 99.50% | Fenoxaprop-P-ethyl is an acetyl-CoA carboxylase (ACC) inhibitor and post-emergence herbicide. Fenoxaprop-P-ethyl inhibits the conversion of acetyl-CoA to malonyl-CoA, reduces malonyl-CoA synthesis and disrupts fatty acid synthesis. Fenoxaprop-P-ethyl disrupts lipid homeostasis through cascaded inhibition of lipid metabolism, decreases total lipid content, downregulates fatty acid elongase genes and inhibits their activity. Fenoxaprop-P-ethyl disrupts fatty acid synthesis in rice seedlings and controls annual monocotyledonous weeds in wheat, durum wheat, rye, triticale and barley fields. | ||||||||||||||||||||
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Fenoxaprop-P-ethyl (Standard) | 99.46% | Fenoxaprop-P-ethyl (Standard) is the analytical standard of Fenoxaprop-P-ethyl. This product is intended for research and analytical applications. | ||||||||||||||||||||
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- [1]. Li JY, et al. Fenoxaprop--ethyl Disrupts Lipid Homeostasis in Rice Seedlings: A Multiomics Study Linking the Inhibition of Acetyl-Coenzyme A Carboxylase with a Coordinated Repression of Fatty Acid Elongation Processes. Journal of agricultural and food chemistry. 2026 Jul 15;74(27):21685-21698. [Content Brief]
- [2]. Álvarez F, et al. Peer review of the pesticide risk assessment of the active substance fenoxaprop-P-ethyl. EFSA journal. European Food Safety Authority. 2024 Nov;22(11):e9053. [Content Brief]
