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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H33NO6
Molecular Weight 455.5433
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 5
Charge 0

SHOW SMILES / InChI
Structure of ERYTHROSKYRIN

SMILES

CC(C)[C@@H]1N(C)C(=O)C(C(=O)\C=C\C=C\C=C\C=C\C=C\[C@@H]2O[C@@H]3C[C@@H](C)O[C@@H]3[C@@H]2O)=C1O

InChI

InChIKey=UIINQEVAMDOHAP-JDFIKZOLSA-N
InChI=1S/C26H33NO6/c1-16(2)22-24(30)21(26(31)27(22)4)18(28)13-11-9-7-5-6-8-10-12-14-19-23(29)25-20(33-19)15-17(3)32-25/h5-14,16-17,19-20,22-23,25,29-30H,15H2,1-4H3/b6-5+,9-7+,10-8+,13-11+,14-12+/t17-,19+,20-,22+,23-,25+/m1/s1

HIDE SMILES / InChI

Molecular Formula C26H33NO6
Molecular Weight 455.5433
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 5
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:21:26 GMT 2025
Edited
by admin
on Mon Mar 31 23:21:26 GMT 2025
Record UNII
55845E73S7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ERYTHROSKYRINE
Preferred Name English
ERYTHROSKYRIN
Common Name English
2,4-PYRROLIDINEDIONE, 3-(11-(HEXAHYDRO-3-HYDROXY-5-METHYLFURO(3,2-B)FURAN-2-YL)-1-HYDROXY-2,4,6,8,10-UNDECAPENTAENYLIDENE)-1-METHYL-5-(1-METHYLETHYL)-, (2S-(2.ALPHA.(1Z(R*),2E,4E,6E,8E,10E),3.ALPHA.,3A.BETA.,5.BETA.,6A.BETA.))-
Systematic Name English
2H-PYRROL-2-ONE, 3-((2E,4E,6E,8E,10E)-11-((2S,3R,3AR,5R,6AR)-HEXAHYDRO-3-HYDROXY-5-METHYLFURO(3,2-B)FURAN-2-YL)-1-OXO-2,4,6,8,10-UNDECAPENTAEN-1-YL)-1,5-DIHYDRO-4-HYDROXY-1-METHYL-5-(1-METHYLETHYL)-, (5S)-
Systematic Name English
2,4-PYRROLIDINEDIONE, 3-((2E,4E,6E,8E,10E)-11-((2S,3R,3AR,5R,6AR)-HEXAHYDRO-3-HYDROXY-5-METHYLFURO(3,2-B)FURAN-2-YL)-1-HYDROXY-2,4,6,8,10-UNDECAPENTAEN-1-YLIDENE)-1-METHYL-5-(1-METHYLETHYL)-, (3Z,5S)-
Systematic Name English
Code System Code Type Description
CAS
4987-27-3
Created by admin on Mon Mar 31 23:21:26 GMT 2025 , Edited by admin on Mon Mar 31 23:21:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID101098372
Created by admin on Mon Mar 31 23:21:26 GMT 2025 , Edited by admin on Mon Mar 31 23:21:26 GMT 2025
PRIMARY
FDA UNII
55845E73S7
Created by admin on Mon Mar 31 23:21:26 GMT 2025 , Edited by admin on Mon Mar 31 23:21:26 GMT 2025
PRIMARY
CAS
132923-00-3
Created by admin on Mon Mar 31 23:21:26 GMT 2025 , Edited by admin on Mon Mar 31 23:21:26 GMT 2025
ALTERNATIVE
CAS
11006-15-8
Created by admin on Mon Mar 31 23:21:26 GMT 2025 , Edited by admin on Mon Mar 31 23:21:26 GMT 2025
SUPERSEDED