Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H9NO2 |
Molecular Weight | 223.2268 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=CC2=C1C(=O)C3=C(C=CC=C3)C2=O
InChI
InChIKey=KHUFHLFHOQVFGB-UHFFFAOYSA-N
InChI=1S/C14H9NO2/c15-11-7-3-6-10-12(11)14(17)9-5-2-1-4-8(9)13(10)16/h1-7H,15H2
Molecular Formula | C14H9NO2 |
Molecular Weight | 223.2268 |
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 |
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Photoinduced random molecular reorientation by nonradiative energy relaxation: an experimental test. | 2004 Nov |
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[Preparation and fluorescence study of anthracene, perylene and 1-aminoanthraquinone colloids]. | 2005 Jan |
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Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
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Development of nonsymmetrical 1,4-disubstituted anthraquinones that are potently active against cisplatin-resistant ovarian cancer cells. | 2005 Oct 20 |
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Synthesis and antitumor activity of 1,8-diaminoanthraquinone derivatives. | 2005 Sep |
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Dissolved natural organic matter (NOM) impacts photosynthetic oxygen production and electron transport in coontail Ceratophyllum demersum. | 2006 Mar 15 |
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Estimation of first excited singlet-state dipole moments of aminoanthraquinones by solvatochromic method. | 2009 Apr |
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1,8-Bis(tos-yloxy)-9,10-anthraquinone. | 2009 Dec 4 |
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Sensitised near-IR lanthanide luminescence exploiting anthraquinone-derived chromophores: syntheses and spectroscopic properties. | 2009 Oct 21 |
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Estrogenic activity of anthraquinone derivatives: in vitro and in silico studies. | 2010 Aug 16 |
|
2-(Dimethyl-amino)-anthraquinone. | 2010 Nov 6 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:41:24 GMT 2023
by
admin
on
Fri Dec 15 17:41:24 GMT 2023
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Record UNII |
N5YYY1NEUI
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Record Status |
Validated (UNII)
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m1681
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