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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H30O11
Molecular Weight 518.5098
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RUBRATOXIN B

SMILES

[H][C@]1(CC2=C([C@H](O)[C@]([H])([C@H](O)CCCCCC)C3=C(C1)C(=O)OC3=O)C(=O)OC2=O)[C@H](O)[C@@H]4CC=CC(=O)O4

InChI

InChIKey=ZJTBTDVZNGBSNG-RETZLTROSA-N
InChI=1S/C26H30O11/c1-2-3-4-5-7-15(27)20-18-13(23(31)36-25(18)33)10-12(21(29)16-8-6-9-17(28)35-16)11-14-19(22(20)30)26(34)37-24(14)32/h6,9,12,15-16,20-22,27,29-30H,2-5,7-8,10-11H2,1H3/t12-,15+,16-,20+,21-,22-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Rubratoxin B induces signs of fatty acid oxidation disorders (FAODs) in mice.
2011 Oct 10
Name Type Language
RUBRATOXIN B
HSDB  
Common Name English
1H-CYCLONONA(1,2-C:5,6-C')DIFURAN-1,3,6,8(4H)-TETRONE, 10- ((3,6-DIHYDRO-6-OXO-2H-PYRAN-2-YL)HYDROXYMETHYL)-5,9,10,11- TETRAHYDRO-4-HYDROXY-5-(1-HYDROXYHEPTYL)-
Systematic Name English
1,5-CYCLONONADIENE-1,2,5,6-TETRACARBOXYLIC 1,2:5,6-DIANHYDRIDE, 8-((3,6-DIHYDRO-6-OXO-2H-PYRAN-2-YL)HYDROXYMETHYL)-3-HYDROXY-4-(1-HYDROXYHEPTYL)-
Systematic Name English
RUBRATOXIN B [HSDB]
Common Name English
1H-CYCLONONA(1,2-C:5,6-C')DIFURAN-1,3,6,8(4H)-TETRONE, 10-((R)-((2R)-3,6-DIHYDRO-6-OXO-2H-PYRAN-2-YL)HYDROXYMETHYL)-5,9,10,11-TETRAHYDRO-4-HYDROXY-5-((1S)-1-HYDROXYHEPTYL)-, (4S,5R,10R)-REL-(+)-
Systematic Name English
10-((3,6-DIHYDRO-6-OXO-2H- PYRAN-2-YL)HYDROXYMETHYL)-5,9,10,11-TETRAHYDRO-4-HYDROXY-5- (1-HYDROXYHEPTYL)-1H-CYCLONONA(1,2-C:5,6-C')DIFURAN- 1,3,6,8(4H)-TETRONE, (4R*,5S*(R*),10S*(S*(S*)))-(+)-
Systematic Name English
NSC-126729
Code English
1H-CYCLONONA(1,2-C:5,6-C')DIFURAN-1,3,6,8(4H)-TETRONE, 10-((3,6-DIHYDRO-6-OXO-2H-PYRAN-2-YL)HYDROXYMETHYL)-5,9,10,11-TETRAHYDRO-4-HYDROXY-5-(1-HYDROXYHEPTYL)-, (4R*,5S*(R*),10S*(S*(S*)))-(+)-
Systematic Name English
Code System Code Type Description
CAS
21794-01-4
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
ECHA (EC/EINECS)
244-582-6
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
PUBCHEM
11969548
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
HSDB
3533
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
WIKIPEDIA
Rubratoxin B
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
FDA UNII
J38U4758MY
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
NSC
126729
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID60101906
Created by admin on Sat Dec 16 08:01:39 GMT 2023 , Edited by admin on Sat Dec 16 08:01:39 GMT 2023
PRIMARY