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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H22O8
Molecular Weight 354.3518
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FUSARENONE X

SMILES

CC(=O)O[C@@H]1[C@@H](O)[C@H]2O[C@@H]3C=C(C)C(=O)[C@@H](O)[C@]3(CO)[C@]1(C)[C@]24CO4

InChI

InChIKey=XGCUCFKWVIWWNW-CAYGJDLQSA-N
InChI=1S/C17H22O8/c1-7-4-9-16(5-18,12(22)10(7)20)15(3)13(24-8(2)19)11(21)14(25-9)17(15)6-23-17/h4,9,11-14,18,21-22H,5-6H2,1-3H3/t9-,11-,12-,13-,14-,15-,16-,17+/m1/s1

HIDE SMILES / InChI

Molecular Formula C17H22O8
Molecular Weight 354.3518
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Apoptosis and gene expression in the developing mouse brain of fusarenon-X-treated pregnant mice.
2014-08-17
Effects of oral exposure to naturally-occurring and synthetic deoxynivalenol congeners on proinflammatory cytokine and chemokine mRNA expression in the mouse.
2014-07-15
Role of cholecystokinin in anorexia induction following oral exposure to the 8-ketotrichothecenes deoxynivalenol, 15-acetyldeoxynivalenol, 3-acetyldeoxynivalenol, fusarenon X, and nivalenol.
2014-04
Comparison of emetic potencies of the 8-ketotrichothecenes deoxynivalenol, 15-acetyldeoxynivalenol, 3-acetyldeoxynivalenol, fusarenon X, and nivalenol.
2013-01
Mechanism-based alternative monitoring of endoplasmic reticulum stress by 8-keto-trichothecene mycotoxins using human intestinal epithelial cell line.
2010-10-20
Relationship of trichothecene structure to COX-2 induction in the macrophage: selective action of type B (8-keto) trichothecenes.
2003-10-24
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:20:52 GMT 2025
Edited
by admin
on Mon Mar 31 22:20:52 GMT 2025
Record UNII
0CV8D1DR96
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-197211
Preferred Name English
FUSARENONE X
Common Name English
NIVALENOL-4-O-ACETATE
Common Name English
3,7,15-TRIHYDROXYSCIRP-4-ACETOXY-9-EN-8-ONE
Common Name English
FUSARENON
Common Name English
3-ACETYLNIVALENOL
Common Name English
TRICHOTHEC-9-EN-8-ONE, 4-(ACETYLOXY)-12,13-EPOXY-3,7,15- TRIHYDROXY-, (3.ALPHA.,4.BETA.,7.BETA.)-
Systematic Name English
4-ACETYLNIVALENOL
Common Name English
TRICHOTHEC-9-EN-8-ONE, 12,13-EPOXY-3.ALPHA.,4.BETA.,7.BETA.,15- TETRAHYDROXY-, 4-ACETATE
Common Name English
4-ACETYLOXY-12,13-EPOXY-3,7,15-TRIHYDROXY-(3-.ALPHA.,4-.BETA.,7- .BETA.)-TRICHOTHEC-9-EN-8-ONE
Common Name English
FUSARENON-X [HSDB]
Common Name English
TRICHOTHEC-9-EN-8-ONE, 4-(ACETYLOXY)-12,13-EPOXY-3,7,15- TRIHYDROXY-, (3-.ALPHA.,4-.BETA.,7-.BETA.)-
Systematic Name English
3,7,15-TRIHYDROXY-4-ACETOXY-8-OXO-12,13-EPOXY-.DELTA.(SUP 9)- TRICHOTHECENE
Common Name English
TRICHOTHEC-9-EN-8-ONE, 12,13-EPOXY-3.ALPHA.,4.BETA.,7.ALPHA.,15-TETRAHYDROXY-, 4-ACETATE
Systematic Name English
12,13-EPOXY-3.ALPHA.,4.BETA.,7.BETA.,15-TETRAHYDROXYTRICHOTHEC-9- EN-8-ONE 4-ACETATE
Common Name English
TRICHOTHEC-9-EN-8-ONE, 4-(ACETYLOXY)-12,13-EPOXY-3,7,15-TRIHYDROXY-, (3.ALPHA.,4.BETA.,7.ALPHA.)-
Systematic Name English
NIVALENOL MONOACETATE
Common Name English
3.ALPHA.,7.ALPHA.,15-TRIHYDROXY-4.BETA.-ACETOXY-12,13- EPOXYTRICHOTHEC-9-EN-8-ONE
Common Name English
4.BETA.-ACETOXY-3.ALPHA.,7.ALPHA.,15-TRIHYDROXY-12,13-EPOXYTRICHOTHEC-9-EN-8-ONE
Systematic Name English
Code System Code Type Description
HSDB
3486
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID1020649
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY
NSC
197211
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY
FDA UNII
0CV8D1DR96
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY
PUBCHEM
304599
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY
CAS
23255-69-8
Created by admin on Mon Mar 31 22:20:52 GMT 2025 , Edited by admin on Mon Mar 31 22:20:52 GMT 2025
PRIMARY