Date published: 2026-5-28

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Fuscin (CAS 83-85-2)

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Alternate Names:
3,4,7,9-Tetrahydroxy-6-methyl-1H-phenalen-1-one
Application:
Fuscin is an anti-HIV compound and CKR-5 (CCR5) antagonist
CAS Number:
83-85-2
Molecular Weight:
276.3
Molecular Formula:
C15H16O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Fuscin, a natural pigment derived from certain fungi, has garnered interest in scientific research for its unique chemical properties and potential applications. Recent studies have delved into its mechanism of action and explored its various research applications. Fuscin has been investigated for its antioxidant properties, showing the ability to scavenge free radicals and protect cells from oxidative stress-induced damage. Moreover, research suggests that fuscin exhibits antimicrobial activity against a wide range of pathogens, including bacteria and fungi, making it a promising candidate for the development of novel antimicrobial agents. Additionally, fuscin has shown potential in environmental research, particularly in the field of bioremediation, where it has been explored for its ability to degrade organic pollutants and mitigate environmental contamination. Furthermore, studies have highlighted its role as a biosynthetic precursor for the synthesis of various organic compounds with diverse chemical structures and potential industrial applications. Overall, fuscin represents a valuable natural product with multifaceted research applications spanning antioxidant, antimicrobial, environmental, and synthetic chemistry fields.


Fuscin (CAS 83-85-2) References

  1. 10-Methoxydihydrofuscin, fuscinarin, and fuscin, novel antagonists of the human CCR5 receptor from Oidiodendron griseum.  |  Yoganathan, K., et al. 2003. J Nat Prod. 66: 1116-7. PMID: 12932138
  2. Studies in the biochemistry of micro-organisms; fuscin, a metabolic product of Oidiodendron fuscum Robak. Part 2. Derivatives and degradation products.  |  BIRKINSHAW, JH., et al. 1951. Biochem J. 48: 67-74. PMID: 14820786
  3. Studies in the biochemistry of micro-organisms. 79. Fuscin, a metabolic product of Oidiodendron fuscum Robak. Part 1. Preparation, properties and antibacterial activity.  |  Michael, SE. 1948. Biochem J. 43: 528-33. PMID: 16748446
  4. Fuscin, an antibacterial pigment from Oidiodendron fuscum Robak.  |  MICHAEL, SE. 1948. Biochem J. 42: xl. PMID: 18863779
  5. Root canal morphology of the mandibular first premolars in an Iranian population using cross-sections and radiography.  |  Khedmat, S., et al. 2010. J Endod. 36: 214-7. PMID: 20113777
  6. Bioactive Metabolites from the Deep Subseafloor Fungus Oidiodendron griseum UBOCC-A-114129.  |  Navarri, M., et al. 2017. Mar Drugs. 15: PMID: 28387732
  7. Antimicrobial and antibiofilm activity of fungal metabolites on methicillin-resistant Staphylococcus aureus (ATCC 43300) mediated by SarA and AgrA.  |  Martínez-Rodríguez, OP., et al. 2023. Biofouling. 39: 830-837. PMID: 37929585
  8. [A new inhibitor, fuscin, in the study of animal and yeast mitochondria respiratory chains].  |  Demaille, J., et al. 1970. Eur J Biochem. 13: 416-27. PMID: 4315418
  9. Fuscin, an inhibitor of mitochondrial SH-dependent transport-linked functions.  |  Vignais, PM. and Vignais, PV. 1973. Biochim Biophys Acta. 325: 357-74. PMID: 4798314
  10. Fuscin, an inhibitor of respiration and oxidative phosphorylation in ox-neck muscle mitochondria.  |  Cheah, KS. 1972. Biochim Biophys Acta. 275: 1-9. PMID: 5049017
  11. Pollen calendar of the city of Salamanca (Spain). Aeropalynological analysis for 1981-1982 and 1991-1992.  |  Hernández Prieto, M., et al. 1998. Allergol Immunopathol (Madr). 26: 209-22. PMID: 9885728

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Fuscin, 1 mg

sc-391101
1 mg
$169.00