Cas no 145040-09-1 (Hydrolyzed Fumonisin B1)

Hydrolyzed Fumonisin B1 is a modified form of Fumonisin B1, a mycotoxin produced by Fusarium fungi. Through hydrolysis, the ester-linked tricarballylic acid side chains are removed, reducing its toxicity while retaining its utility in research applications. This derivative is particularly valuable in analytical studies, serving as a reference standard for detecting and quantifying fumonisins in food and feed samples. Its hydrolyzed structure enhances stability and facilitates precise measurement in chromatographic and immunological assays. Researchers utilize Hydrolyzed Fumonisin B1 to develop mitigation strategies for mycotoxin contamination, ensuring food safety and regulatory compliance. Its well-characterized properties make it a reliable tool for toxicological and metabolic investigations.
Hydrolyzed Fumonisin B1 structure
Hydrolyzed Fumonisin B1 structure
Product Name:Hydrolyzed Fumonisin B1
CAS No:145040-09-1
MF:C22H47NO5
MW:405.612287759781
CID:153625
Update Time:2025-08-04

Hydrolyzed Fumonisin B1 Chemical and Physical Properties

Names and Identifiers

    • (2S,3S,5R,10R,12S,14S,15R,16R)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol
    • 3,5,10,14,15-Eicosanepentol,2-amino-12,16-dimethyl-, (2S,3S,5R,10R,12S,14S,15R,16R)-
    • (2S,3S,5R,10S,12R,14R,15S,16S)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol
    • 3,5,10,14,15-Eicosanepentol, 2-amino-12,16-dimethyl-, (2S-(2R*,3R*,5S*,10S*,12R*,14R*,15S*,16S*))-
    • Aminopentol
    • Aminopentol formate salt
    • AP1 Metabolite
    • Hydrolyzed Fumonisin B1
    • Inchi: 1S/C22H47NO5/c1-5-6-9-16(3)22(28)21(27)13-15(2)12-18(24)10-7-8-11-19(25)14-20(26)17(4)23/h15-22,24-28H,5-14,23H2,1-4H3/t15-,16+,17+,18+,19-,20+,21-,22+/m1/s1
    • InChI Key: UWWVLQOLROBFTD-OFFHYKNXSA-N
    • SMILES: O[C@@H]([C@H]([C@@H](C)CCCC)O)C[C@H](C)C[C@H](CCCC[C@H](C[C@@H]([C@H](C)N)O)O)O

Computed Properties

  • Exact Mass: 405.34561
  • Monoisotopic Mass: 405.345
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 6
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 28
  • Rotatable Bond Count: 17
  • Complexity: 371
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 8
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 127A^2

Experimental Properties

  • Density: 1.051
  • Boiling Point: 593.8°Cat760mmHg
  • Flash Point: 312.9°C
  • Refractive Index: 1.507
  • PSA: 127.17

Hydrolyzed Fumonisin B1 Pricemore >>

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Additional information on Hydrolyzed Fumonisin B1

Hydrolyzed Fumonisin B1: A Comprehensive Overview

Fumonisin B1 (FB1) is a mycotoxin produced by the fungus Aspergillus flavus and Aspergillus parasiticus, which are commonly found in contaminated agricultural products such as corn and peanuts. FB1 is a well-known toxin that poses significant risks to both human and animal health. However, Hydrolyzed Fumonisin B1 represents a processed form of this toxin, often utilized in research and analytical contexts to study its properties and effects. This article delves into the latest research findings, applications, and implications of Hydrolyzed Fumonisin B1, providing a detailed and up-to-date analysis.

The CAS No 145040-09-1 corresponds to Hydrolyzed Fumonisin B1, which is derived through hydrolysis of the parent compound. This process involves breaking down the molecular structure of FB1, often to isolate specific components or to reduce its toxicity for experimental purposes. Recent studies have focused on understanding the structural changes that occur during hydrolysis and how these modifications affect the biological activity of the compound.

One of the most significant advancements in research on Hydrolyzed Fumonisin B1 is its application in understanding the mechanisms of mycotoxin toxicity. Scientists have utilized this compound to study how FB1 interacts with cellular pathways, particularly those involved in lipid metabolism and cell signaling. For instance, recent findings suggest that Hydrolyzed Fumonisin B1 disrupts sphingolipid biosynthesis, leading to cellular dysfunction and apoptosis. These insights have profound implications for developing strategies to mitigate mycotoxin-related health risks.

In addition to its role in basic research, Hydrolyzed Fumonisin B1 has been instrumental in the development of diagnostic tools for detecting mycotoxin contamination in food and feed. Researchers have employed this compound as a standard in immunoassays and other analytical techniques to ensure accurate detection limits and reproducibility. The use of Hydrolyzed Fumonisin B1 in these applications underscores its importance in ensuring food safety and regulatory compliance.

Another area of active investigation is the environmental impact of Hydrolyzed Fumonisin B1. Studies have explored its persistence in soil and water systems, as well as its potential effects on non-target organisms. Recent research indicates that while hydrolysis reduces the acute toxicity of FB1, residual compounds may still pose ecological risks under certain conditions. These findings highlight the need for further studies to assess long-term environmental impacts.

The application of Hydrolyzed Fumonisin B1 extends into therapeutic research as well. Scientists are exploring whether modified forms of FB1 could be repurposed for medical uses, such as targeting specific pathological processes. For example, some studies suggest that certain derivatives of Hydrolyzed Fumonisin B1 may exhibit anti-cancer properties by modulating key signaling pathways involved in tumor progression.

In conclusion, Hydrolyzed Fumonisin B1 (CAS No 145040-09-1) is a critical compound in both research and applied settings. Its role in understanding mycotoxin toxicity, developing diagnostic tools, assessing environmental impacts, and exploring therapeutic potentials underscores its significance across multiple disciplines. As research continues to uncover new insights into its properties and applications, Hydrolyzed Fumonisin B1 remains a focal point for advancing knowledge in mycotoxicology and related fields.

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