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Details

Stereochemistry RACEMIC
Molecular Formula C13H14N2O
Molecular Weight 214.2631
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VELNACRINE

SMILES

NC1=C2C=CC=CC2=NC3=C1C(O)CCC3

InChI

InChIKey=HLVVITIHAZBPKB-UHFFFAOYSA-N
InChI=1S/C13H14N2O/c14-13-8-4-1-2-5-9(8)15-10-6-3-7-11(16)12(10)13/h1-2,4-5,11,16H,3,6-7H2,(H2,14,15)

HIDE SMILES / InChI

Molecular Formula C13H14N2O
Molecular Weight 214.2631
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 17:27:14 UTC 2023
Edited
by admin
on Fri Dec 15 17:27:14 UTC 2023
Record UNII
Y2P6NV151K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VELNACRINE
INN   MI   WHO-DD  
INN  
Official Name English
1-ACRIDINOL, 9-AMINO-1,2,3,4-TETRAHYDRO-, (±)-
Systematic Name English
1-HYDROXYTACRINE
Common Name English
HYDROXYTACRINE
Common Name English
9-AMINO-1,2,3,4-TETRAHYDROACRIDIN-1-OL
Systematic Name English
1-ACRIDINOL, 9-AMINO-1,2,3,4-TETRAHYDRO-
Systematic Name English
VELNACRINE [MI]
Common Name English
(±)-9-AMINO-1,2,3,4-TETRAHYDRO-1-ACRIDINOL
Systematic Name English
velnacrine [INN]
Common Name English
1-OH-THA
Common Name English
Velnacrine [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47792
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL51934
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
MERCK INDEX
m983
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY Merck Index
CAS
104675-29-8
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
SUPERSEDED
PUBCHEM
3655
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
MESH
C056424
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
FDA UNII
Y2P6NV151K
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
SMS_ID
100000079097
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
INN
6403
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
EVMPD
SUB00033MIG
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
EPA CompTox
DTXSID4046945
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
DRUG CENTRAL
3848
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
CAS
124027-47-0
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
NCI_THESAURUS
C96773
Created by admin on Fri Dec 15 17:27:14 UTC 2023 , Edited by admin on Fri Dec 15 17:27:14 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> METABOLITE ACTIVE
URINE
Related Record Type Details
ACTIVE MOIETY