283159-90-0
Chemical Structure
Valifenalate
Synonym(s): IR5885; Valiphenal
- CAS. Nr.: 283159-90-0
- Formula:C19H27ClN2O5
- Molecular Weight:398.88
IUPAC Name: methyl 3-(4-chlorophenyl)-3-((S)-2-((isopropoxycarbonyl)amino)-3-methylbutanamido)propanoate
InChIKey: DBXFMOWZRXXBRN-LWKPJOBUSA-N
SMILES: O=C([C@H](C(C)C)NC(OC(C)C)=O)NC(C1=CC=C(Cl)C=C1)CC(OC)=O
Biological Activity: Valifenalate (IR5885; Valiphenal) is an insecticide agent and fungicide, which is approved for application on high-value crops such as grapes, tomatoes and other vegetables. Valifenalate interferes with cell-wall synthesisValifenalate is effective against various types of mildew. Valifenalate can be used against crown rot of rose cuased by Phytophthora citrophthora. Valifenalate induces non-adverse thyroid changes via adaptive induction of uridine 5’-diphosphoglucuronosyltransferase (UGT) in the liver of dogs and rats[1][2][3].
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Valifenalate | 98.09% | Valifenalate (IR5885; Valiphenal) is an insecticide agent and fungicide, which is approved for application on high-value crops such as grapes, tomatoes and other vegetables. Valifenalate interferes with cell-wall synthesisValifenalate is effective against various types of mildew. Valifenalate can be used against crown rot of rose cuased by Phytophthora citrophthora. Valifenalate induces non-adverse thyroid changes via adaptive induction of uridine 5’-diphosphoglucuronosyltransferase (UGT) in the liver of dogs and rats. | ||||||||||||||||||||
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Valifenalate (Standard) | ≥98% | Valifenalate (Standard) is the analytical standard of Valifenalate. This product is intended for research and analytical applications. Valifenalate (IR5885; Valiphenal) is an insecticide agent and fungicide, which is approved for application on high-value crops such as grapes, tomatoes and other vegetables. Valifenalate interferes with cell-wall synthesisValifenalate is effective against various types of mildew. Valifenalate can be used against crown rot of rose cuased by Phytophthora citrophthora. Valifenalate induces non-adverse thyroid changes via adaptive induction of uridine 5’-diphosphoglucuronosyltransferase (UGT) in the liver of dogs and rats. | ||||||||||||||||||||
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References
- [1]. HOFFMAN, Thomas, James., et al. FUNGICIDAL COMPOSITIONS. WO 2018 219773 A1
- [2]. A. Salamone, et al., Efficacy of the fungicide valifenalate against crown rot of rose caused by Phytophthora citrophthora. Modern fungicides and antifungal compounds VII. Proceedings of the 17th International Reinhardsbrunn Symposium, April 21-25 2013, 2014.
- [3]. Christine Walter, et al., Valifenalate-induced non-adverse thyroid changes via adaptive induction of uridine 5′-diphospho-glucuronosyltransferase (UGT) in the liver of dogs and rats but not humans. Toxicology and Applied Pharmacology, 2025.
