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Details

Stereochemistry ABSOLUTE
Molecular Formula C37H40N2O6
Molecular Weight 608.7233
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXYACANTHINE

SMILES

COC1=CC2=C3[C@H](CC4=CC=C(OC5=C(O)C=CC(C[C@H]6N(C)CCC7=CC(OC)=C(OCC3=C1O)C=C67)=C5)C=C4)N(C)CC2

InChI

InChIKey=KFOTVHQUFWAKNY-IHLOFXLRSA-N
InChI=1S/C37H40N2O6/c1-38-13-11-24-18-33(42-3)34-20-27(24)29(38)16-23-7-10-31(40)32(17-23)45-26-8-5-22(6-9-26)15-30-36-25(12-14-39(30)2)19-35(43-4)37(41)28(36)21-44-34/h5-10,17-20,29-30,40-41H,11-16,21H2,1-4H3/t29-,30+/m1/s1

HIDE SMILES / InChI

Molecular Formula C37H40N2O6
Molecular Weight 608.7233
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Free radical scavenging activity and lipoxygenase inhibition of Mahonia aquifolium extract and isoquinoline alkaloids.
2007-07-16
Antimicrobial activity of Mahonia aquifolium and two of its alkaloids against oral bacteria.
2007
A comparative study on the anti-inflammatory, antinociceptive and antipyretic effects of isoquinoline alkaloids from the roots of Turkish Berberis species.
2002-12-27
Potential antimutagenic activity of berberine, a constituent of Mahonia aquifolium.
2002-02-19
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:23:30 GMT 2025
Edited
by admin
on Mon Mar 31 20:23:30 GMT 2025
Record UNII
5BD0KNF4AT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-93135
Preferred Name English
OXYACANTHINE
MI  
Common Name English
OXYACANTHAN-12'-OL, 6,6',7-TRIMETHOXY-2,2'-DIMETHYL-
Common Name English
OXYACANTHINE [MI]
Common Name English
N-METHYLOCOTEAMINE
Common Name English
VINETINE
Common Name English
6,6',7-TRIMETHOXY-2,2'-DIMETHYL-OXYACANTHAN-12'-OL
Common Name English
2H-1,24:12,15-DIETHENO-6,10-METHENO-16H-PYRIDO(2',3':17,18)(1,10)DIOXACYCLOEICOSINO(2,3,4-IJ)ISOQUINOLIN-9-OL, 3,4,4A,5,16A,17,18,19-OCTAHYDRO-21,22,26-TRIMETHOXY-4,17-DIMETHYL-, (4AR,16AS)-
Common Name English
N-METHYLSEPEERINE
Common Name English
OXYACANTHINE, (+)-
Common Name English
OXYCANTHINE
Common Name English
(+)-OXYACANTHINE
Common Name English
Code System Code Type Description
NSC
93135
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
MESH
C092646
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-946-8
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
MERCK INDEX
m8322
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY Merck Index
PUBCHEM
73415
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID40893514
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
CHEBI
7853
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
CAS
548-40-3
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY
FDA UNII
5BD0KNF4AT
Created by admin on Mon Mar 31 20:23:30 GMT 2025 , Edited by admin on Mon Mar 31 20:23:30 GMT 2025
PRIMARY