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Details

Stereochemistry ACHIRAL
Molecular Formula C13H9NO
Molecular Weight 195.2167
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACRIDONE

SMILES

O=C1C2=C(NC3=C1C=CC=C3)C=CC=C2

InChI

InChIKey=FZEYVTFCMJSGMP-UHFFFAOYSA-N
InChI=1S/C13H9NO/c15-13-9-5-1-3-7-11(9)14-12-8-4-2-6-10(12)13/h1-8H,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C13H9NO
Molecular Weight 195.2167
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Presence and fate of carbamazepine, oxcarbazepine, and seven of their metabolites at wastewater treatment plants.
2009-04
Synthesis of N-4-butylamine acridone and its use as fluorescent probe for ctDNA.
2009-01-01
Biotransformation of acridine by Mycobacterium vanbaalenii.
2009-01
Synthesis, cytotoxic activity, and mechanism of action of furo[2,3-c]acridin-6-one and benzo[b]furo[3,2-h]acridin-6-one analogues of psorospermin and acronycine.
2008-11-27
Chloro acridone derivatives as cytotoxic agents active on multidrug-resistant cell lines and their duplex DNA complex studies by electrospray ionization mass spectrometry.
2008-11-25
Hybridization biosensor using 2-nitroacridone as electrochemical indicator for detection of short DNA species of Chronic Myelogenous Leukemia.
2008-11-15
New acridone-4-carboxylic acid derivatives as potential inhibitors of hepatitis C virus infection.
2008-10-01
Potential anti-allergic acridone alkaloids from the roots of Atalantia monophylla.
2008-10
Application of chitin and chitosan as elicitors of coumarins and fluoroquinolone alkaloids in Ruta graveolens L. (common rue).
2008-10
Synthesis and potent antileukemic activities of 10-benzyl-9(10H)-acridinones.
2008-09-15
Design, synthesis and preliminary biological evaluation of acridine compounds as potential agents for a combined targeted chemo-radionuclide therapy approach to melanoma.
2008-08-15
Novel fluorinated acridone derivatives. Part 1: synthesis and evaluation as potential anticancer agents.
2008-07-15
Acridone-tagged DNA as a new probe for DNA detection by fluorescence resonance energy transfer and for mismatch DNA recognition.
2008-07-15
Unusually divergent 4-coumarate:CoA-ligases from Ruta graveolens L.
2008-07
Chronic exposure of the oligochaete Lumbriculus variegatus to polycyclic aromatic compounds (PACs): bioavailability and effects on reproduction.
2008-05-01
Cooperativity in intramolecular bifurcated hydrogen bonds: an ab initio study.
2008-04-17
Life cycle responses of the midge Chironomus riparius to polycyclic aromatic compound exposure.
2008-03
Quinoline, quinazoline and acridone alkaloids.
2008-02
Anthranilate N-methyltransferase, a branch-point enzyme of acridone biosynthesis.
2008-02
SAR of a series of anti-HSV-1 acridone derivatives, and a rational acridone-based design of a new anti-HSV-1 3H-benzo[b]pyrazolo[3,4-h]-1,6-naphthyridine series.
2008-01-01
Combining G-quadruplex targeting motifs on a single peptide nucleic acid scaffold: a hybrid (3+1) PNA-DNA bimolecular quadruplex.
2008
Synthesis and evaluation of N-substituted acridones as antiviral agents against haemorrhagic fever viruses.
2008
Substrate arrays for fluorescence-based enzyme fingerprinting and high-throughput screening.
2008
Design, synthesis and biological evaluation of new oligopyrrole carboxamides linked with tricyclic DNA-intercalators as potential DNA ligands or topoisomerase inhibitors.
2007-06
Acridone derivatives: design, synthesis, and inhibition of breast cancer resistance protein ABCG2.
2007-04-15
Modulation of P-glycoprotein activity by acridones and coumarins from Citrus sinensis.
2007-04
Acridine and acridone derivatives, anticancer properties and synthetic methods: where are we now?
2007-03
Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae) of southern Africa.
2007-03
Chemico-enzymatic synthesis of a new fluorescent-labeled DNA by PCR with a thymidine nucleotide analogue bearing an acridone derivative.
2007-02-01
Quinoline, quinazoline and acridone alkaloids.
2007-02
An acridone-producing novel multifunctional type III polyketide synthase from Huperzia serrata.
2007-02
[From acronycine to benzo-[b]-acronycine derivatives: potent antitumor agents].
2007-01
In vitro cytotoxicity activity on several cancer cell lines of acridone alkaloids and N-phenylethyl-benzamide derivatives from Swinglea glutinosa (Bl.) Merr.
2007-01
Investigation of cytotoxic activity on human cancer cell lines of arborinine and furanoacridones isolated from Ruta graveolens.
2007-01
Synthesis and structure-activity studies of peptide-acridine/acridone conjugates.
2007
Electroenzymatic polypyrrole-intercalator sensor for the determination of West Nile virus cDNA.
2006-10-01
Evaluation and lead optimization of anti-malarial acridones.
2006-09
Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity.
2006-08-15
Synthesis of acridone derivatives using polymer-supported palladium and scandium catalysts.
2006-07-11
Synthesis and anti-BVDV activity of acridones as new potential antiviral agents.
2006-04-20
Spectrophotometric determination and computational evaluation of the rates of hydrolysis of 9-amino-substituted acridines.
2006-03-28
Anionic N-fries rearrangement of N-carbamoyl diarylamines to anthranilamides. Methodology and application to acridone and pyranoacridone alkaloids.
2006-03-16
Alpha-glucosidase inhibitory and antioxidant acridone alkaloids from the stem bark of Oriciopsis glaberrima ENGL. (Rutaceae).
2006-03
Sensitization of multidrug resistant (MDR) cancer cells to vinblastine by novel acridones: correlation between anti-calmodulin activity and anti-MDR activity.
2006-01
Design, synthesis and antiproliferative activity of some new azapyranoxanthenone aminoderivatives.
2006-01
Synthesis and properties of acridone-labeled base-discriminating fluorescent (BDF) nucleosides.
2006
Synthesis and property of DNA labeled with fluorescent acridone.
2006
Liquid chromatography-electrospray mass spectrometry determination of carbamazepine, oxcarbazepine and eight of their metabolites in human plasma.
2005-12-15
Astonishing diversity of natural surfactants: 6. Biologically active marine and terrestrial alkaloid glycosides.
2005-11
Quinoline, quinazoline and acridone alkaloids.
2005-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:30:04 GMT 2025
Edited
by admin
on Mon Mar 31 19:30:04 GMT 2025
Record UNII
6BK306GUQA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACRIDONE
Systematic Name English
OXCARBAZEPINE RELATED COMPOUND C
USP   USP-RS  
Preferred Name English
10H-ACRIDIN-9-ONE
Systematic Name English
NSC-408196
Code English
OXCARBAZEPINE RELATED COMPOUND C [USP IMPURITY]
Common Name English
OXCARBAZEPINE RELATED COMPOUND C [USP-RS]
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1483185
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
PUBCHEM
2015
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
MESH
C041300
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID8060371
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
FDA UNII
6BK306GUQA
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-434-7
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
WIKIPEDIA
ACRIDONE
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
CAS
578-95-0
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY
NSC
408196
Created by admin on Mon Mar 31 19:30:04 GMT 2025 , Edited by admin on Mon Mar 31 19:30:04 GMT 2025
PRIMARY