Antifungal agent 175
Antifungal agent 175 is a potent antifungal agent with an EC50 of 1.8 μg/mL against R. solani. Antifungal agent 175 Z17 exerts its effects primarily by disrupting the cell membranes of pathogenic fungi to trigger lipid peroxidation and oxidative stress, inhibiting pyruvate kinase (PK) to interfere with energy metabolism, and binding to the cytochrome bc1 complex. Antifungal agent 175 can be used in research on rice sheath blight.
For research use only. We do not sell to patients.
- Formula: C27H28ClF3N4O3S2
- Molecular Weight:613.11
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
Antifungal agent 175 (compound Z17) potently inhibits the mycelial growth of various phytopathogenic fungi, with the strongest activity against Rhizoctonia solani, with an EC50 value of 1.8 μg/mL[1].
Antifungal agent 175 (1.56-25 μg/mL; 24 h) potently and concentration-dependently inhibits sclerotial germination of Rhizoctonia solani[1].
Antifungal agent 175 potently inhibits the mycelial growth of Rhizoctonia solani, Phomopsis sp., Sclerotinia sclerotiorum, Botrytis cinerea, Phytophthora capsica, Valsa mali, and Botryosphaeria dothidea, with EC50 values ranging from 1.8 μg/mL to 14.9 μg/mL[1].
Antifungal agent 175 (25-50 μg/mL) disrupts the membrane integrity of Rhizoctonia solani mycelia and induces intracellular reactive oxygen species accumulation in a concentration-dependent manner[1].
Antifungal agent 175 (3.125-25 μg/mL) reduces the pyruvate content and pyruvate kinase activity in Rhizoctonia solani in a dose-dependent manner, indicating that it interferes with cellular energy metabolism[1].
Antifungal agent 175 forms an extensive interaction network with the cytochrome bc1 complex and creates a stable complex[1].
Antifungal agent 175 (50-200 μg/mL; 24 h seed soaking followed by 7 days of incubation) exerts no significant effect on seed germination, root length, or shoot length of Oryza sativa L.[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Rhizoctonia solani
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Concentration:1.56, 3.125, 6.25, 12.5, 25 μg/mL
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Incubation Time:24 h
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Result:Potently inhibited the sclerotial germination of Rhizoctonia solani in a concentration-dependent manner.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:earthworm[1]
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Dosage:10 μg/mL; 20 μg/mL
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Administration:topical application to filter paper; single dose; 48 h
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Result:Exhibited survival counts and survival rates comparable to the control group.
Chemical Information
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Molecular Weight 613.11
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Formula C27H28ClF3N4O3S2
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SMILES
S=C(N1CCC(N(CCCN(C/2=O)C(SC2=C/C3=CC=C(OC(F)(F)F)C=C3)=O)C)CC1)NC4=CC=CC(Cl)=C4
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- Antifungal agent 175
- Antifungal agent175
- Antifungal agent-175
- Fungal
- Reactive Oxygen Species (ROS)
- Pyruvate Kinase
- Cytochrome P450
- rice sheath blight
- Oryza sativa L.
- Phomopsis sp.
- Sclerotinia sclerotiorum
- Valsa mali
- Rhizoctonia solani
- Botrytis cinerea
- Botryosphaeria dothidea
- cytochrome bc1 complex
- Phytophthora capsica
- Inhibitor
- inhibitor
- inhibit