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Details

Stereochemistry RACEMIC
Molecular Formula C13H16N2O2
Molecular Weight 232.2783
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TASIPIMIDINE

SMILES

COC1=C2CCOC(C3=NCCN3)C2=CC=C1

InChI

InChIKey=GHIKYGQWBRHEGU-UHFFFAOYSA-N
InChI=1S/C13H16N2O2/c1-16-11-4-2-3-10-9(11)5-8-17-12(10)13-14-6-7-15-13/h2-4,12H,5-8H2,1H3,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C13H16N2O2
Molecular Weight 232.2783
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 Sat Dec 16 16:18:54 GMT 2023
Edited
by admin
on Sat Dec 16 16:18:54 GMT 2023
Record UNII
QX8MJH6HGK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TASIPIMIDINE
USAN   INN  
Official Name English
1H-IMIDAZOLE, 2-(3,4-DIHYDRO-5-METHOXY-1H-2-BENZOPYRAN-1-YL)-4,5-DIHYDRO-
Systematic Name English
tasipimidine [INN]
Common Name English
RAC-2-((1R)-5-METHOXY-3,4-DIHYDRO-1H-2-BENZOPYRAN-1-YL)-4,5-DIHYDRO-1H-IMIDAZOLE
Systematic Name English
TASIPIMIDINE [USAN]
Common Name English
ORM-19695
Code English
ODM-105
Code English
Classification Tree Code System Code
NCI_THESAURUS C29709
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
Code System Code Type Description
SMS_ID
300000023682
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
CAS
1465908-70-6
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
INN
10623
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
NCI_THESAURUS
C152516
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
PUBCHEM
71767208
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
FDA UNII
QX8MJH6HGK
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
USAN
GH-106
Created by admin on Sat Dec 16 16:18:54 GMT 2023 , Edited by admin on Sat Dec 16 16:18:54 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
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ACTIVE MOIETY