Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C2N=CC=CC2=C(C=C1)N=O
InChI
InChIKey=RZWRYPGAUIOOMK-UHFFFAOYSA-N
InChI=1S/C9H6N2O2/c12-8-4-3-7(11-13)6-2-1-5-10-9(6)8/h1-5,12H
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| 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 |
|---|---|---|
| Actions of a histone deacetylase inhibitor NSC3852 (5-nitroso-8-quinolinol) link reactive oxygen species to cell differentiation and apoptosis in MCF-7 human mammary tumor cells. | 2006-05 |
|
| Differentiation-inducing quinolines as experimental breast cancer agents in the MCF-7 human breast cancer cell model. | 2004-11-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 22:20:40 GMT 2025
by
admin
on
Tue Apr 01 22:20:40 GMT 2025
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| Record UNII |
P302KW5VDN
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| Record Status |
Validated (UNII)
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| Record Version |
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222-650-6
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19103
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3852
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DTXSID5063079
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3565-26-2
Created by
admin on Tue Apr 01 22:20:40 GMT 2025 , Edited by admin on Tue Apr 01 22:20:40 GMT 2025
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P302KW5VDN
Created by
admin on Tue Apr 01 22:20:40 GMT 2025 , Edited by admin on Tue Apr 01 22:20:40 GMT 2025
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