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Details

Stereochemistry ACHIRAL
Molecular Formula C14H10N2O2
Molecular Weight 238.2414
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-DIAMINOANTHRAQUINONE

SMILES

NC1=CC=C2C(=O)C3=C(C=CC=C3)C(=O)C2=C1N

InChI

InChIKey=LRMDXTVKVHKWEK-UHFFFAOYSA-N
InChI=1S/C14H10N2O2/c15-10-6-5-9-11(12(10)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,15-16H2

HIDE SMILES / InChI

Molecular Formula C14H10N2O2
Molecular Weight 238.2414
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Endogenous nitric oxide is a key promoting factor for initiation of seizure-like events in hippocampal and entorhinal cortex slices.
2009-07-01
2-(4-Methyl-phen-yl)-1H-anthraceno[1,2-d]imidazole-6,11-dione: a fluorescent chemosensor.
2009-04-18
Synthesis of new naphtho[2,3-f]quinoxaline-2,7,12(1H)-trione and anthra-9,10-quinone dyes from furan-2,3-diones.
2009-04-02
Floral transition and nitric oxide emission during flower development in Arabidopsis thaliana is affected in nitrate reductase-deficient plants.
2008-07
Spectroscopic studies of 1,2-diaminoanthraquinone (DAQ) as a fluorescent probe for the imaging of nitric oxide in living cells.
2008-01
[Detection of NO-synthase activity of lactobacilli by fluorescent staining].
2007-11-03
Microbial transformation of amino- and hydroxyanthraquinones by Beauveria bassiana ATCC 7159.
2006-10
Synthesis and evaluation of a new non-fluorescent quencher in fluorogenic oligonucleotide probes for real-time PCR.
2005-07-21
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
Electronic absorption spectra of amino substituted anthraquinones and their interpretation using the ZINDO/S and AM1 methods.
2003-05
Nitric oxide modulates low-Mg2+-induced epileptiform activity in rat hippocampal-entorhinal cortex slices.
2002-10
Spatial nitric oxide imaging using 1,2-diaminoanthraquinone to investigate the involvement of nitric oxide in long-term potentiation in rat brain slices.
2002-03
Direct nitric oxide imaging in cultured hippocampal neurons with diaminoanthraquinone and confocal microscopy.
2001
Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase.
1995-11-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:40:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:40:13 GMT 2025
Record UNII
H5P6YP29VA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2-DIAMINOANTHRAQUINONE
Systematic Name English
NSC-39934
Preferred Name English
9,10-ANTHRACENEDIONE, 1,2-DIAMINO-
Systematic Name English
ANTHRAQUINONE, 1,2-DIAMINO-
Systematic Name English
Code System Code Type Description
FDA UNII
H5P6YP29VA
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
MESH
C118201
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID5061950
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
NSC
39934
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
217-156-2
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
PUBCHEM
15652
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY
CAS
1758-68-5
Created by admin on Mon Mar 31 19:40:13 GMT 2025 , Edited by admin on Mon Mar 31 19:40:13 GMT 2025
PRIMARY