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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H26O8
Molecular Weight 382.4049
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEOSOLANIOL

SMILES

CC(=O)OC[C@]12C[C@H](O)C(C)=C[C@H]1O[C@@H]3[C@H](O)[C@@H](OC(C)=O)[C@@]2(C)[C@]34CO4

InChI

InChIKey=TVZHDVCTOCZDNE-WVJYZQHISA-N
InChI=1S/C19H26O8/c1-9-5-13-18(6-12(9)22,7-24-10(2)20)17(4)15(26-11(3)21)14(23)16(27-13)19(17)8-25-19/h5,12-16,22-23H,6-8H2,1-4H3/t12-,13+,14+,15+,16+,17+,18+,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H26O8
Molecular Weight 382.4049
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Structure-function relationship of T-2 toxin and its metabolites in inducing thymic apoptosis in vivo in mice.
1998-08
Experimental trichothecene mycotoxicosis produced in broiler chickens by Fusarium sporotrichiella var. sporotrichioides.
1982
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:17:14 GMT 2025
Edited
by admin
on Mon Mar 31 22:17:14 GMT 2025
Record UNII
PLZ86LH7A6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-197212
Preferred Name English
NEOSOLANIOL
Common Name English
NEOZOLANIOL
Common Name English
SOLANIOL
Common Name English
TRICHOTHEC-9-ENE-3,4,8,15-TETROL, 12,13-EPOXY-, 4,15-DIACETATE, (3.ALPHA.,4.BETA.,8.ALPHA.)-
Systematic Name English
Code System Code Type Description
PUBCHEM
13818797
Created by admin on Mon Mar 31 22:17:14 GMT 2025 , Edited by admin on Mon Mar 31 22:17:14 GMT 2025
PRIMARY
NSC
197212
Created by admin on Mon Mar 31 22:17:14 GMT 2025 , Edited by admin on Mon Mar 31 22:17:14 GMT 2025
PRIMARY
EPA CompTox
DTXSID40891813
Created by admin on Mon Mar 31 22:17:14 GMT 2025 , Edited by admin on Mon Mar 31 22:17:14 GMT 2025
PRIMARY
CAS
36519-25-2
Created by admin on Mon Mar 31 22:17:14 GMT 2025 , Edited by admin on Mon Mar 31 22:17:14 GMT 2025
PRIMARY
FDA UNII
PLZ86LH7A6
Created by admin on Mon Mar 31 22:17:14 GMT 2025 , Edited by admin on Mon Mar 31 22:17:14 GMT 2025
PRIMARY