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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
Constituents of the root bark of Severinia buxifolia collected in Hainan.
2001 Aug
Quinoline, quinazoline and acridone alkaloids.
2001 Oct
Synthesis and antitumor activity of conjugates of muramyldipeptide, normuramyldipeptide, and desmuramylpeptides with acridine/acridone derivatives.
2001 Oct 25
The antiviral agent 5-chloro-1,3-dihydroxyacridone interferes with assembly and maturation of herpes simplex virus.
2002 Feb
Development of a precolumn derivatization method for the determination of free amines in wastewater by high-performance liquid chromatography via fluorescent detection with 9-(2-hydroxyethyl)acridone.
2002 Jan 1
Synthesis and chemical characterization of 2-methoxy-N(10)-substituted acridones needed to reverse vinblastine resistance in multidrug resistant (MDR) cancer cells.
2002 Jul
DNA-binding antitumor agents: from pyrimido[5,6,1-de]acridines to other intriguing classes of acridine derivatives.
2002 Sep
Ratiometric probes for hydrogencarbonate analysis in intracellular or extracellular environments using europium luminescence.
2002 Sep 7
Chemiluminescence in autoxidation of phosphonate carbanions. Phospha-1,2-dioxetanes as the most likely high-energy intermediates.
2003 Jul 25
Antiproliferative constituents in plants 14. Coumarins and acridone alkaloids from Boenninghausenia japonica NAKAI.
2004 Aug
Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives.
2004 Aug
Synthesis of C8-linked pyrrolo[2,1-c][1,4]benzodiazepine-acridone/acridine hybrids as potential DNA-binding agents.
2004 Aug 2
Tetrapeptides induce selective recognition for G-quadruplexes when conjugated to a DNA-binding platform.
2004 Oct 21
Spectrophotometric determination of the dissociation constants of crown ethers with grafted acridone unit in methanol based on Benesi-Hildebrand evaluation.
2005 Dec
N-Substituted acridone alkaloids from Toddaliopsis bremekampii (Rutaceae: Toddalioideae) of south-central Africa.
2005 Jul
Quinoline, quinazoline and acridone alkaloids.
2005 Oct
Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity.
2006 Aug 15
Sensitization of multidrug resistant (MDR) cancer cells to vinblastine by novel acridones: correlation between anti-calmodulin activity and anti-MDR activity.
2006 Jan
Anionic N-fries rearrangement of N-carbamoyl diarylamines to anthranilamides. Methodology and application to acridone and pyranoacridone alkaloids.
2006 Mar 16
Spectrophotometric determination and computational evaluation of the rates of hydrolysis of 9-amino-substituted acridines.
2006 Mar-Apr
Electroenzymatic polypyrrole-intercalator sensor for the determination of West Nile virus cDNA.
2006 Oct 1
Synthesis and structure-activity studies of peptide-acridine/acridone conjugates.
2007
Substrate arrays for fluorescence-based enzyme fingerprinting and high-throughput screening.
2008
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 Nov 27
Application of chitin and chitosan as elicitors of coumarins and fluoroquinolone alkaloids in Ruta graveolens L. (common rue).
2008 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:00:41 UTC 2023
Edited
by admin
on Fri Dec 15 19:00:41 UTC 2023
Record UNII
6BK306GUQA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACRIDONE
Systematic 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
OXCARBAZEPINE RELATED COMPOUND C
USP   USP-RS  
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1483185
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
PUBCHEM
2015
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
MESH
C041300
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
EPA CompTox
DTXSID8060371
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
FDA UNII
6BK306GUQA
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-434-7
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
WIKIPEDIA
ACRIDONE
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
CAS
578-95-0
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY
NSC
408196
Created by admin on Fri Dec 15 19:00:42 UTC 2023 , Edited by admin on Fri Dec 15 19:00:42 UTC 2023
PRIMARY