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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
Structure of 1-AMINOANTHRAQUINONE

SMILES

NC1=C2C(=O)C3=C(C=CC=C3)C(=O)C2=CC=C1

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

HIDE SMILES / InChI
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

Unknown
149124
PubMed

PubMed

TitleDatePubMed
2-(Dimethyl-amino)-anthraquinone.
2010-11-06
Estrogenic activity of anthraquinone derivatives: in vitro and in silico studies.
2010-08-16
1,8-Bis(tos-yloxy)-9,10-anthraquinone.
2009-12-04
Sensitised near-IR lanthanide luminescence exploiting anthraquinone-derived chromophores: syntheses and spectroscopic properties.
2009-10-21
Estimation of first excited singlet-state dipole moments of aminoanthraquinones by solvatochromic method.
2009-04
Treatment of bromoamine acid wastewater using combined process of micro-electrolysis and biological aerobic filter.
2009-03-15
Photoreduction of 2-methyl-1-nitro-9,10-anthraquinone in the presence of 1-phenylethanol.
2008-11
Identification of novel protein kinase CK1 delta (CK1delta) inhibitors through structure-based virtual screening.
2008-10-15
Dynamic evolution of light-induced orientation of dye-doped liquid crystals in liquid phase studied by time-resolved optically heterodyned optical Kerr effect technique.
2008-02-28
A new entry to polycyclic indole derivatives via intramolecular imino Diels-Alder reaction: observation of unexpected reaction.
2007-04-27
Intramolecular hydrogen bonding in 1,8-dihydroxyanthraquinone, 1-aminoanthraquinone, and 9-hydroxyphenalenone studied by picosecond time-resolved fluorescence spectroscopy in a supersonic jet.
2006-10-12
Microbial transformation of amino- and hydroxyanthraquinones by Beauveria bassiana ATCC 7159.
2006-10
Synthesis of 7-oxo-7H-naphtho[1,2,3-de]quinoline derivatives as potential anticancer agents active on multidrug resistant cell lines.
2006-05-01
Dissolved natural organic matter (NOM) impacts photosynthetic oxygen production and electron transport in coontail Ceratophyllum demersum.
2006-03-15
Spectrofluorometric study of complexation of some amino derivatives of 9,10-anthraquinone with beta-cyclodextrin.
2005-11
Development of nonsymmetrical 1,4-disubstituted anthraquinones that are potently active against cisplatin-resistant ovarian cancer cells.
2005-10-20
Synthesis and antitumor activity of 1,8-diaminoanthraquinone derivatives.
2005-09
Probing excited-state dynamics and intramolecular proton transfer in 1-acylaminoanthraquinones via the intermolecular solvent response.
2005-08-18
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
[Preparation and fluorescence study of anthracene, perylene and 1-aminoanthraquinone colloids].
2005-01
Photoinduced random molecular reorientation by nonradiative energy relaxation: an experimental test.
2004-11
Dispersion of organic pigments using supercritical carbon dioxide.
2004-02-01
Synthesis and cytotoxic activity of 7-oxo-7H-dibenz[f,ij]isoquinoline and 7-oxo-7H-benzo[e]perimidine derivatives.
2001-06-07
Patents

Patents

03959318
1
03984425
1
04054586
1
04105680
1
JP2000200683A
1
JP2000229947A
1
JP2002534542A
2
JPH05117215A
1
JPH055023A
1
JPH07157674A
1
JPH07233330A
1
JPS5268169A
1
JPS5298738A
1
JPS55142053A
1
JPS58118547A
1
JPS58131965A
1
JPS601169A
1
JPS61204272A
1
JPS63169394A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:50:29 GMT 2025
Edited
by admin
on Mon Mar 31 18:50:29 GMT 2025
Record UNII
N5YYY1NEUI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-30415
Preferred Name English
1-AMINOANTHRAQUINONE
MI  
Systematic Name English
1-AMINO-9,10-ANTHRAQUINONE
Systematic Name English
AMINOANTHRAQUINONE, 1-
Systematic Name English
NSC-458
Code English
9,10-ANTHRACENEDIONE, 1-AMINO-
Systematic Name English
1-AMINOANTHRAQUINONE [MI]
Common Name English
ANTHRAQUINONE, 1-AMINO-
Systematic Name English
1-AMINO-9,10-ANTHRACENEDIONE
Systematic Name English
Code System Code Type Description
NSC
30415
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-423-5
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID2052572
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
NSC
458
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
PUBCHEM
6710
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
CAS
82-45-1
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
MERCK INDEX
m1681
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY Merck Index
FDA UNII
N5YYY1NEUI
Created by admin on Mon Mar 31 18:50:29 GMT 2025 , Edited by admin on Mon Mar 31 18:50:29 GMT 2025
PRIMARY
NIH
NCATS
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