U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H22N2
Molecular Weight 278.3914
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EBURNAMENINE

SMILES

[H][C@@]12N3CCC[C@]1(CC)C=CN4C5=C(C=CC=C5)C(CC3)=C24

InChI

InChIKey=VKTOXAGUZWAECL-RBUKOAKNSA-N
InChI=1S/C19H22N2/c1-2-19-9-5-11-20-12-8-15-14-6-3-4-7-16(14)21(13-10-19)17(15)18(19)20/h3-4,6-7,10,13,18H,2,5,8-9,11-12H2,1H3/t18-,19+/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H22N2
Molecular Weight 278.3914
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:57:00 GMT 2023
Edited
by admin
on Sat Dec 16 16:57:00 GMT 2023
Record UNII
LB9CWH9GJ2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EBURNAMENINE
Common Name English
EBURNAMENINE, (+)-
Common Name English
(13AR-CIS)-13A-ETHYL-2,3,5,6,13A,13B-HEXAHYDRO-1H-INDOLO(3,2,1-DE)PYRIDO(3,2,1-IJ)(1,5)NAPHTHYRIDINE
Systematic Name English
1H-INDOLO(3,2,1-DE)PYRIDO(3,2,1-IJ)(1,5)NAPHTHYRIDINE, 13A-ETHYL-2,3,5,6,13A,13B-HEXAHYDRO-, (13AR-CIS)-
Systematic Name English
(+)-EBURNAMENINE
Common Name English
Code System Code Type Description
PUBCHEM
6857502
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID201046055
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
CAS
517-30-6
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
FDA UNII
LB9CWH9GJ2
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
WIKIPEDIA
Eburnamenine
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
CHEBI
35644
Created by admin on Sat Dec 16 16:57:00 GMT 2023 , Edited by admin on Sat Dec 16 16:57:00 GMT 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER