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

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H28O7
Molecular Weight 416.4642
Optical Activity UNSPECIFIED
Additional Stereochemistry Yes
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0
Stereo Comments AXIAL, R

SHOW SMILES / InChI
Structure of BESIGOMSIN

SMILES

COC1=C(OC)C(OC)=C2C(C[C@](C)(O)[C@@H](C)CC3=C2C(OC)=C4OCOC4=C3)=C1

InChI

InChIKey=ZWRRJEICIPUPHZ-MYODQAERSA-N
InChI=1S/C23H28O7/c1-12-7-13-8-16-20(30-11-29-16)22(28-6)17(13)18-14(10-23(12,2)24)9-15(25-3)19(26-4)21(18)27-5/h8-9,12,24H,7,10-11H2,1-6H3/t12-,23-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H28O7
Molecular Weight 416.4642
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 17:40:41 UTC 2023
Edited
by admin
on Sat Dec 16 17:40:41 UTC 2023
Record UNII
L5U70J87J8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BESIGOMSIN
INN   JAN  
INN  
Official Name English
besigomsin [INN]
Common Name English
SCHISANTHERINOL B
Common Name English
WUWEIZICHUN B
Common Name English
(+)-GOMISIN A
Common Name English
TJN-101
Code English
GOMISIN A
Common Name English
(+)-(6S,7S, BIAR-R)-5,6,7,8-TETRAHYDRO-1,2,3,13-TETRAMETHOXY-6,7-DIMETHYLBENZO(3,4)CYCLOOCTA(1,2-F)(1,3)BENZODIOXOL-6-OL
Common Name English
SCHISANDROL B (GOMISIN A) (CONSTITUENT OF NORTHERN SCHISANDRA) [DSC]
Common Name English
SCHIZANDROL B
Common Name English
TJN 101
Code English
BENZO(3,4)CYCLOOCTA(1,2-F)(1,3)BENZODIOXOL-6-OL, 5,6,7,8-TETRAHYDRO-1,2,3,13-TETRAMETHOXY-6,7-DIMETHYL-, (6S,7S,13AR)-
Systematic Name English
WUWEIZI ALCOHOL B
Common Name English
BESIGOMSIN [JAN]
Common Name English
SCHISANDROL B
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C2080
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL403578
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
CAS
58546-54-6
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
FDA UNII
L5U70J87J8
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
SMS_ID
100000086072
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
WIKIPEDIA
Gomisin A
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
NCI_THESAURUS
C74244
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
INN
7001
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
PUBCHEM
3001662
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
EPA CompTox
DTXSID7048950
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
EVMPD
SUB05787MIG
Created by admin on Sat Dec 16 17:40:41 UTC 2023 , Edited by admin on Sat Dec 16 17:40:41 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
USP
Related Record Type Details
ACTIVE MOIETY