67564-91-4
Chemical Structure
Fenpropimorph
- CAS No.: 67564-91-4
- Formula:C20H33NO
- Molecular Weight:303.48
IUPAC Name: (2S,6R)-4-(3-(4-(tert-butyl)phenyl)-2-methylpropyl)-2,6-dimethylmorpholine
InChIKey: RYAUSSKQMZRMAI-ALOPSCKCSA-N
SMILES: C[C@H](O[C@@H](C1)C)CN1CC(C)CC2=CC=C(C=C2)C(C)(C)C
Biological Activity: Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fenpropimorph | 98.74% | Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells. | ||||||||||||||||||||
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Fenpropimorph (Standard) | ≥98% | Fenpropimorph (Standard) is the analytical standard of Fenpropimorph. This product is intended for research and analytical applications. Fenpropimorph is a fungicide that inhibits the sterol pathway. Fenpropimorph inhibits δ8-δ7-sterol isomerase in yeast at low concentrations, with δ14-sterol reductase being blocked at higher levels, preventing the biosynthesis of ergosterol. Fenpropimorph also inhibits sterol synthesis in certain plants and mammalian cells. | ||||||||||||||||||||
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Similarity Score 0.91
HY-121169Amorolfine -
Similarity Score 0.90
HY-B0238RAmorolfine hydrochloride (Standard) -
Similarity Score 0.90
HY-W391940(Rac)-Amorolfine hydrochloride -
Similarity Score 0.76
HY-126200RFenpropidin (Standard) -
Similarity Score 0.65
HY-145897NMDA-IN-2 -
Similarity Score 0.63
![1-[3-(4-tert-Butylbenzoyl)propyl]-4-hydroxypiperidine (Standard) Chemical Structure](//file.medchemexpress.com/product_pic/hy-z6838r.gif)
HY-Z6838R1-[3-(4-tert-Butylbenzoyl)propyl]-4-hydroxypiperidine (Standard) -
Similarity Score 0.62
HY-128469Inaperisone -
Similarity Score 0.61
HY-128891Eperisone -
Similarity Score 0.61
HY-B1901REperisone hydrochloride (Standard) -
Explore the MedChemAI to find more analogs
![1-[3-(4-tert-Butylbenzoyl)propyl]-4-hydroxypiperidine (Standard) Chemical Structure](http://file.medchemexpress.com/product_pic/hy-z6838r.gif)
References
- [1]. Costet MF, et al. Ecdysteroid biosynthesis and embryonic development are disturbed in insects (Locusta migratoria) reared on plant diet (Triticum sativum) with a selectively modified sterol profile. Proc Natl Acad Sci U S A. 1987;84(3):643-647. [Content Brief]
- [2]. Marcireau C, et al. In vivo effects of fenpropimorph on the yeast Saccharomyces cerevisiae and determination of the molecular basis of the antifungal property. Antimicrob Agents Chemother. 1990;34(6):989-993. [Content Brief]
- [3]. Corio-Costet MF, et al. Inhibition by the fungicide fenpropimorph of cholesterol biosynthesis in 3T3 fibroblasts. Biochem J. 1988;256(3):829-834. [Content Brief]
