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
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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 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
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
