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

Details

Stereochemistry RACEMIC
Molecular Formula C20H20N2O
Molecular Weight 304.3856
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SURONACRINE

SMILES

OC1CCCC2=C1C(NCC3=CC=CC=C3)=C4C=CC=CC4=N2

InChI

InChIKey=HERUZAOANPGYSY-UHFFFAOYSA-N
InChI=1S/C20H20N2O/c23-18-12-6-11-17-19(18)20(15-9-4-5-10-16(15)22-17)21-13-14-7-2-1-3-8-14/h1-5,7-10,18,23H,6,11-13H2,(H,21,22)

HIDE SMILES / InChI

Molecular Formula C20H20N2O
Molecular Weight 304.3856
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Suronacrine (also known as HP128) is a tetrahydroacridinol derivative patented by Hoechst-Roussel Pharmaceuticals, Inc for the treatment of various memory dysfunctions characterized by decreased cholinergic function. The activity ofHP128 is attributable to its inhibition of both norepinephrine uptake and cholinesterase enzyme activity. Suronacrine has enhanced memory in animals with combined cholinergic and adrenergic lesions. In preclinical models, Suronacrine blocks responses to nerve stimulation and to carbachol, but increased responses to acetylcholine. Extracellular recording of nerve terminal currents from triangularis sterni preparations revealed that Suronacrine had a selective blocking action on the waveform associated with K+ currents.

Approval Year

Sample Use Guides

100 mg twice daily
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:17:33 GMT 2023
Edited
by admin
on Sat Dec 16 17:17:33 GMT 2023
Record UNII
BW1184480X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SURONACRINE
INN  
INN  
Official Name English
suronacrine [INN]
Common Name English
1-ACRIDINOL, 1,2,3,4-TETRAHYDRO-9-((PHENYLMETHYL)AMINO)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C47792
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID70869429
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
NCI_THESAURUS
C96775
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
INN
6404
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
EVMPD
SUB10784MIG
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
FDA UNII
BW1184480X
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
CAS
157789-18-9
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
SUPERSEDED
SMS_ID
100000082988
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
MESH
C070061
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
CAS
104675-35-6
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
ChEMBL
CHEMBL301958
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
CAS
121445-19-0
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
SUPERSEDED
PUBCHEM
60601
Created by admin on Sat Dec 16 17:17:33 GMT 2023 , Edited by admin on Sat Dec 16 17:17:33 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY