Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CCC2=CC=CC=C2N1
InChI
InChIKey=TZOYXRMEFDYWDQ-UHFFFAOYSA-N
InChI=1S/C9H9NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-4H,5-6H2,(H,10,11)
| Molecular Formula | C9H9NO |
| Molecular Weight | 147.1739 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Potent dihydroquinolinone dopamine D2 partial agonist/serotonin reuptake inhibitors for the treatment of schizophrenia. | 2010-05-01 |
|
| Ethyl 6-chloro-2-oxo-4-phenyl-1,2-dihydro-quinoline-3-carboxyl-ate. | 2009-11-04 |
|
| Synthesis of highly enantioenriched 3,4-dihydroquinolin-2-ones by 6-exo-trig radical cyclizations of axially chiral alpha-halo-ortho-alkenyl anilides. | 2009-10-28 |
|
| (RS)-3-Acetyl-2-methyl-4-(3-nitro-phen-yl)-1,4,5,6,7,8-hexa-hydro-quinolin-5-one. | 2009-09-26 |
|
| Novel approach to 3,4-dihydro-2(1H)-quinolinone derivatives via cyclopropane ring expansion. | 2009-03-05 |
|
| In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-1H-quinolin-2-one derivatives. | 2008-12-25 |
|
| Comparison of the bioactivation potential of the antidepressant and hepatotoxin nefazodone with aripiprazole, a structural analog and marketed drug. | 2008-06 |
|
| Synthesis and biological activity of quinolinone and dihydroquinolinone p38 MAP kinase inhibitors. | 2008-03-15 |
|
| Quinoline and derivatives at a tar oil contaminated site: hydroxylated products as indicator for natural attenuation? | 2007-08-01 |
|
| Development of potent, orally active 1-substituted-3,4-dihydro-2-quinolone glycogen phosphorylase inhibitors. | 2007-01-15 |
|
| Synthesis and SAR of highly potent and selective dopamine D(3)-receptor antagonists: Quinolin(di)one and benzazepin(di)one derivatives. herve.geneste@abbott.com. | 2006-02 |
|
| Synthesis of five-, six-, and seven-membered ring lactams by CpRh complex-catalyzed oxidative N-heterocyclization of amino alcohols. | 2004-08-05 |
|
| Novel 3,4-dihydroquinolin-2(1H)-one inhibitors of human glycogen phosphorylase a. | 2003-12-15 |
|
| Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter: Part 3. A potential 5-HT transporter imaging agent, 3-(3-[18F]fluoropropyl)-6-nitroquipazine. | 2003-11-17 |
|
| Radical ring closures of 4-isocyanato carbon-centered radicals. | 2003-04-04 |
|
| Synthesis and vasorelaxing evaluation of alpha-methylidene-gamma-butyrolactone bearing quinolin-2(1H)-one and 3,4-dihydroquinolin-2(1H)-one derivatives. | 2002-01-05 |
|
| Synthesis of 3-methoxycarbonylmethyl derivatives of dihydroquinolone and dihydrochromenone. | 2001-03-23 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:22:18 GMT 2025
by
admin
on
Mon Mar 31 21:22:18 GMT 2025
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| Record UNII |
2CKG6TX32F
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| Record Status |
Validated (UNII)
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