57646-30-7
Chemical Structure
Furalaxyl
Synonym(s): CGA 38140
- CAS No.: 57646-30-7
- Formula:C17H19NO4
- Molecular Weight:301.34
IUPAC Name: methyl N-(2,6-dimethylphenyl)-N-(furan-2-carbonyl)alaninate
InChIKey: CIEXPHRYOLIQQD-UHFFFAOYSA-N
SMILES: O=C(C(C)N(C1=C(C)C=CC=C1C)C(C2=CC=CO2)=O)OC
Biological Activity: Furalaxyl (CGA 38140) is an acylalanine fungicide with high selectivity against the order Peronosporales. Furalaxyl inhibits mycelial growth of Pythium ultimum. Furalaxyl inhibits fungal protein and nucleic acid synthesis, with RNA synthesis being more strongly inhibited than DNA synthesis. The primary mode of action of Furalaxyl is considered to involve impairment of fungal RNA biosynthesis and associated effects on mitosis. Furalaxyl is applicable for studies on oomycete growth inhibition, fungal RNA biosynthesis, and pesticide photodegradation[1][2][3].
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Furalaxyl | Furalaxyl (CGA 38140) is an acylalanine fungicide with high selectivity against the order Peronosporales. Furalaxyl inhibits mycelial growth of Pythium ultimum. Furalaxyl inhibits fungal protein and nucleic acid synthesis, with RNA synthesis being more strongly inhibited than DNA synthesis. The primary mode of action of Furalaxyl is considered to involve impairment of fungal RNA biosynthesis and associated effects on mitosis. Furalaxyl is applicable for studies on oomycete growth inhibition, fungal RNA biosynthesis, and pesticide photodegradation. | |||||||||||||||||||||
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Furalaxyl (Standard) | ≥98% | Furalaxyl (Standard) is the analytical standard of Furalaxyl. This product is intended for research and analytical applications. Furalaxyl (CGA 38140) is a potent fungicide. Furalaxyl is highly selective to fungi of the order of the Peronosporales. | ||||||||||||||||||||
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References
- [1]. Iesce MR, et al. Sensitized photooxygenation of the fungicide furalaxyl. Environmental science and pollution research international. 2004;11(4):222-6.
- [2]. Fisher DJ, et al. Mode of action of the systemic fungicides furalaxyl, metalaxyl and ofurace. Pesticide Science. 1982;13(3):330-339.
- [3]. Kerkenaar A, et al. Antifungal activity of metalaxyl and furalaxyl. Pesticide Biochemistry and Physiology. 1981;15(1):71-78.
