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Fusarenon X
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Fusarenon X

CAS: 23255-69-8

Ref. 3D-BF162730

1mg
734.00 €
5mg
2,796.00 €
10mg
4,474.00 €
Estimated delivery in United States, on Monday 21 Apr 2025

Product Information

Name:
Fusarenon X
Synonyms:
  • (3Beta,4Alpha,6Beta,11Xi)-3,7,15-Trihydroxy-8-Oxo-12,13-Epoxytrichothec-9-En-4-Yl Acetate
  • (3Beta,4Alpha,7Alpha)-3,7,15-Trihydroxy-8-Oxo-12,13-Epoxytrichothec-9-En-4-Yl Acetate
  • (3α,4β,7α)-4-(Acetyloxy)-12,13-epoxy-3,7,15-trihydroxytrichothec-9-en-8-one
  • 12,13-Epoxy-3-alpha,4-beta,7-beta,15-tetrahydroxytrichothec-9-en-8-one 4-acetate
  • 12,13-Epoxy-3alpha,4beta,7beta,15-tetrahydroxytrichothec-9-en-8-one 4-acetate
  • 3,7,15-Trihydroxy-4-acetoxy-8-oxo-12,13-epoxy-delta(sup 9)-trichothecene
  • 3,7,15-Trihydroxyscirp-4-acetoxy-9-en-8-one
  • 3-Acetylnivalenol
  • 3alpha,7alpha,15-Trihydroxy-4beta-acetoxy-12,13-epoxytrichothec-9-en-8-one
  • 4-Acetylnivalenol
  • See more synonyms
  • 4-Acetyloxy-12,13-epoxy-3,7,15-trihydroxy-(3-alpha,4-beta,7-beta)-trichothec-9-en-8-one
  • 4β-Acetoxy-3α,7α,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
  • Ccris 4922
  • Fusarenon
  • Fusarenone
  • Fusarenone X
  • Hsdb 3486
  • Nivalenol monoacetate
  • Nivalenol-4-O-acetate
  • Nsc 197211
  • Spiro[2,5-methano-1-benzoxepin-10,2′-oxirane], trichothec-9-en-8-one deriv.
  • Trichothec-9-en-8-one, 12,13-epoxy-3alpha,4beta,7beta,15-tetrahydroxy-, 4-acetate
  • Trichothec-9-en-8-one, 12,13-epoxy-3alpha,4beta,7beta,15-tetrahydroxy-, 4-acetate (8CI)
  • Trichothec-9-en-8-one, 12,13-epoxy-3α,4β,7α,15-tetrahydroxy-, 4-acetate
  • Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-, (3-alpha,4-beta,7-beta)-
  • Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-, (3alpha,4beta,7beta)-
  • Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-, (3α,4β,7α)-
Description:

Fusarenon X is an antimicrobial agent that belongs to the class of macrolides. It is a synthetic antibiotic that is active against bacteria, such as Bacillus subtilis, Escherichia coli, and Staphylococcus aureus. The sample preparation procedure includes extracting the sample with trifluoroacetic acid in order to remove lipids and other interferences that may interfere with the analysis. Fusarenon X is analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS). The polymerase chain reaction (PCR) amplification of DNA was used as a control for this analysis. This antibiotic binds to bacterial ribosomes and inhibits protein synthesis by binding to 16S ribosomal RNA. It also has shown strong antimicrobial activity against hl-60 cells in vitro.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Purity:
Min. 95%
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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