Date published: 2025-12-15

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Strobilurin B (CAS 65105-52-4)

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Alternate Names:
Methyl (2E,3Z,5E)-6-(4-chloro-3-methoxy-phenyl)-2-(methoxymethylidene)-3-methyl-hexa-3,5-dienoate; (2E,3Z,5E)-Methyl-6-(4-chloro-3-methoxyphenyl)-2-(methoxy-methylene)-3-methylhexa-3,5-dienoate
Application:
Strobilurin B is an antifungal agent that acts by inhibiting mitochondrial respiration in fungi
CAS Number:
65105-52-4
Purity:
≥97%
Molecular Weight:
322.8
Molecular Formula:
C17H19ClO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Strobilurin B is a naturally occurring fungicidal compound, part of the strobilurin class of pesticides, which were first identified as extracts from wood-decaying fungi of the strobilurin group. This compound specifically inhibits mitochondrial respiration in fungi by binding to the ubiquinol oxidation site of complex III in the mitochondrial electron transport chain. This action blocks electron transfer, which is crucial for cellular energy production, leading to a cessation of ATP synthesis and ultimately resulting in fungal cell death. In research, strobilurin B has been extensively used to study the bioenergetic processes of fungal cells, providing insights into mitochondrial dynamics and the mechanisms of energy production in eukaryotic organisms. Its role as a mitochondrial inhibitor also makes it a useful tool in examining the physiological effects of respiratory inhibition in cells, including the study of reactive oxygen species (ROS) production and the induction of programmed cell death pathways. Furthermore, research involving strobilurin B has contributed to understanding how fungi develop resistance to fungicides, helping to explain genetic adaptations that confer resistance, which is crucial for the development of new strategies to manage and circumvent resistance in pathogenic fungi. Through these applications, strobilurin B not only enhances knowledge in fungal physiology but also aids in the advancement of agricultural sciences by informing more effective fungicide use strategies.


Strobilurin B (CAS 65105-52-4) References

  1. Total synthesis of strobilurin B using a hetero-bis-metallated pentadiene linchpin.  |  Coleman, RS. and Lu, X. 2006. Chem Commun (Camb). 423-5. PMID: 16493822
  2. Bioactive metabolites from cultures of basidiomycete Favolaschia tonkinensis.  |  Kornsakulkarn, J., et al. 2010. J Nat Prod. 73: 759-62. PMID: 20329738
  3. Investigations into the biosynthesis of the antifungal strobilurins.  |  Iqbal, Z., et al. 2018. Org Biomol Chem. 16: 5524-5532. PMID: 30027987
  4. Strobilurin biosynthesis in Basidiomycete fungi.  |  Nofiani, R., et al. 2018. Nat Commun. 9: 3940. PMID: 30258052
  5. Natural Compound-derived Cytochrome bc1 Complex Inhibitors as Antifungal Agents.  |  Musso, L., et al. 2020. Molecules. 25: PMID: 33036496
  6. In vitro screening of 65 mycotoxins for insecticidal potential.  |  Boguś, MI., et al. 2021. PLoS One. 16: e0248772. PMID: 33735295
  7. Tumor necrosis factor induces pathogenic mitochondrial ROS in tuberculosis through reverse electron transport.  |  Roca, FJ., et al. 2022. Science. 376: eabh2841. PMID: 35737799
  8. A simplified and easy-to-use HIP HOP assay provides insights into chalcone antifungal mechanisms of action.  |  Prescott, TAK., et al. 2022. FEBS Lett. 596: 3087-3102. PMID: 36053795
  9. Do mitochondria use efflux pumps to protect their ribosomes from antibiotics?  |  Islam, MD., et al. 2023. Microbiology (Reading). 169: PMID: 36748523
  10. Strobilurin X acts as an anticancer drug by inhibiting protein synthesis and suppressing mitochondrial respiratory chain activity.  |  Takahashi, K., et al. 2024. Discov Oncol. 15: 177. PMID: 38769217

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Strobilurin B, 500 µg

sc-364141
500 µg
$163.00

Strobilurin B, 1 mg

sc-364141A
1 mg
$260.00