1246818-14-3
Chemical Structure
Propiconazole-d7
- CAS No.: 1246818-14-3
- Formula:C15H10D7Cl2N3O2
- Molecular Weight:349.26
IUPAC Name: 1-((2-(2,4-dichlorophenyl)-4-(propyl-d7)-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole
InChIKey: STJLVHWMYQXCPB-NCKGIQLSSA-N
SMILES: C(C1(OC(C(C(C([2H])([2H])[2H])([2H])[2H])([2H])[2H])CO1)C2=C(Cl)C=C(Cl)C=C2)N3C=NC=N3
Biological Activity: Propiconazole-d7 is the deuterium labeled Propiconazole. Propiconazole is a broad-spectrum triazole fungicide that inhibits the conversion of lanosterol to ergosterol, leading to fungal cell membrane disruption. Propiconazole inhibits S. cerevisiae, but not rat liver, microsomal cytochrome P450 (IC50s=0.04 and >200 μM, respectively). Propiconazole inhibits the growth of T. deformans and R. stolonifer (ED50s=0.073 and 4.6 μg/mL, respectively). Propiconazole increases production of reactive oxygen species (ROS)[1].
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Propiconazole-d7 | Propiconazole-d7 is the deuterium labeled Propiconazole. Propiconazole is a broad-spectrum triazole fungicide that inhibits the conversion of lanosterol to ergosterol, leading to fungal cell membrane disruption. Propiconazole inhibits S. cerevisiae, but not rat liver, microsomal cytochrome P450 (IC50s=0.04 and >200 μM, respectively). Propiconazole inhibits the growth of T. deformans and R. stolonifer (ED50s=0.073 and 4.6 μg/mL, respectively). Propiconazole increases production of reactive oxygen species (ROS). | |||||||||||||||||||||
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Propiconazole (Standard) | 98.53% | Propiconazole (Standard) is the analytical standard of Propiconazole. This product is intended for research and analytical applications. Propiconazole is an orally active N-substituted triazole used as a fungicide. Propiconazole is a mouse liver hepatotoxicant and a hepatocarcinogen that has adverse reproductive and developmental toxicities in experimental animals. | ||||||||||||||||||||
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Propiconazole-d3 nitrate | Propiconazole-d3 (nitrate) is the deuterium labeled Propiconazole nitrate. Propiconazole is a broad-spectrum triazole fungicide that inhibits the conversion of lanosterol to ergosterol, leading to fungal cell membrane disruption. Propiconazole inhibits S. cerevisiae, but not rat liver, microsomal cytochrome P450 (IC50s=0.04 and >200 µM, respectively). Propiconazole inhibits the growth of T. deformans and R. stolonifer (ED50s=0.073 and 4.6 µg/mL, respectively). Propiconazole increases production of reactive oxygen species (ROS). | |||||||||||||||||||||
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Propiconazole | 98.56% | Propiconazole is an orally active N-substituted triazole used as a fungicide. Propiconazole is a mouse liver hepatotoxicant and a hepatocarcinogen that has adverse reproductive and developmental toxicities in experimental animals. | ||||||||||||||||||||
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