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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

[H][C@@]12CC3=CC=C(O)C(OC4=CC=C(C[C@]5([H])N(C)CCC6=CC(OC)=C(O)C(COC7=CC1=C(CCN2C)C=C7OC)=C56)C=C4)=C3

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

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 22:04:11 GMT 2023
Edited
by admin
on Fri Dec 15 22:04:11 GMT 2023
Record UNII
5BD0KNF4AT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
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
NSC-93135
Code 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 Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
MESH
C092646
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-946-8
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
MERCK INDEX
m8322
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY Merck Index
PUBCHEM
73415
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID40893514
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
CHEBI
7853
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
CAS
548-40-3
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY
FDA UNII
5BD0KNF4AT
Created by admin on Fri Dec 15 22:04:12 GMT 2023 , Edited by admin on Fri Dec 15 22:04:12 GMT 2023
PRIMARY