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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
MOL RATIO 1 MOL RATIO (average)
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

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

In Vivo Use Guide
100 mg twice daily
Route of Administration: Oral
Substance Class Chemical
Record UNII
BW1184480X
Record Status Validated (UNII)
Record Version