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

Details

Stereochemistry RACEMIC
Molecular Formula C20H25NO
Molecular Weight 295.4186
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLEMANSERIN

SMILES

OC(C1CCN(CCC2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=AXNGJCOYCMDPQG-UHFFFAOYSA-N
InChI=1S/C20H25NO/c22-20(18-9-5-2-6-10-18)19-12-15-21(16-13-19)14-11-17-7-3-1-4-8-17/h1-10,19-20,22H,11-16H2

HIDE SMILES / InChI

Molecular Formula C20H25NO
Molecular Weight 295.4186
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:51:13 UTC 2023
Edited
by admin
on Fri Dec 15 15:51:13 UTC 2023
Record UNII
X96LS7MC5Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLEMANSERIN
INN   USAN  
USAN   INN  
Official Name English
glemanserin [INN]
Common Name English
MDL-11,939
Code English
4-PIPERIDINEMETHANOL, .ALPHA.-PHENYL-1-(2-PHENYLETHYL)-, (±)-
Systematic Name English
MDL-11939
Code English
MDL 11,939
Code English
(±)-1-PHENETHYL-.ALPHA.-PHENYL-4-PIPERIDINEMETHANOL
Systematic Name English
GLEMANSERIN [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66885
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
Code System Code Type Description
WIKIPEDIA
Glemanserin
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
CAS
132553-86-7
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
INN
6990
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
USAN
Z-62
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
EVMPD
SUB07912MIG
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
MESH
C066169
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
SMS_ID
100000080401
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
PUBCHEM
71781
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
FDA UNII
X96LS7MC5Z
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
NCI_THESAURUS
C95216
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
ChEMBL
CHEMBL18972
Created by admin on Fri Dec 15 15:51:13 UTC 2023 , Edited by admin on Fri Dec 15 15:51:13 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY