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Details

Stereochemistry RACEMIC
Molecular Formula C14H12N4O.ClH
Molecular Weight 288.732
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RS-8359 HYDROCHLORIDE

SMILES

Cl.OC1CCC2=C1N=CN=C2NC3=CC=C(C=C3)C#N

InChI

InChIKey=TTZWBGBYPWZYSC-UHFFFAOYSA-N
InChI=1S/C14H12N4O.ClH/c15-7-9-1-3-10(4-2-9)18-14-11-5-6-12(19)13(11)16-8-17-14;/h1-4,8,12,19H,5-6H2,(H,16,17,18);1H

HIDE SMILES / InChI

Molecular Formula C14H12N4O
Molecular Weight 252.2713
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro-in vivo correlation for intrinsic clearance for drugs metabolized by human aldehyde oxidase.
2010-08
Genetic polymorphism of aldehyde oxidase in Donryu rats.
2007-05
Chiral inversion of RS-8359: a selective and reversible MAO-A inhibitor via oxido-reduction of keto-alcohol.
2006-09
Enantioselective 2-hydroxylation of RS-8359, a selective and reversible MAO-A inhibitor, by cytochrome P450 in mouse and rat liver microsomes.
2006-08
Stereoselective pharmacokinetics of RS-8359, a selective and reversible MAO-A inhibitor, by species-dependent drug-metabolizing enzymes.
2005-03
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:51:14 GMT 2025
Edited
by admin
on Mon Mar 31 21:51:14 GMT 2025
Record UNII
8T4B4CQD32
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZONITRILE, 4-((6,7-DIHYDRO-7-HYDROXY-5H-CYCLOPENTAPYRIMIDIN-4-YL)AMINO)-, MONOHYDROCHLORIDE
Preferred Name English
RS-8359 HYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
86278292
Created by admin on Mon Mar 31 21:51:14 GMT 2025 , Edited by admin on Mon Mar 31 21:51:14 GMT 2025
PRIMARY
FDA UNII
8T4B4CQD32
Created by admin on Mon Mar 31 21:51:14 GMT 2025 , Edited by admin on Mon Mar 31 21:51:14 GMT 2025
PRIMARY
CAS
214148-18-2
Created by admin on Mon Mar 31 21:51:14 GMT 2025 , Edited by admin on Mon Mar 31 21:51:14 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY