Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H12N4O |
| Molecular Weight | 252.2713 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1CCC2=C1N=CN=C2NC3=CC=C(C=C3)C#N
InChI
InChIKey=YKTSVZRWKHWINV-UHFFFAOYSA-N
InChI=1S/C14H12N4O/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)
| 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 | ( + / - ) |
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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:49:20 GMT 2025
by
admin
on
Mon Mar 31 21:49:20 GMT 2025
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| Record UNII |
79U9T1HIX9
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| Record Status |
Validated (UNII)
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| Record Version |
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164116
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79U9T1HIX9
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DTXSID80909466
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admin on Mon Mar 31 21:49:20 GMT 2025 , Edited by admin on Mon Mar 31 21:49:20 GMT 2025
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105365-76-2
Created by
admin on Mon Mar 31 21:49:20 GMT 2025 , Edited by admin on Mon Mar 31 21:49:20 GMT 2025
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| Related Record | Type | Details | ||
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