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Details

Stereochemistry ACHIRAL
Molecular Formula C13H8OS
Molecular Weight 212.267
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIOXANTHONE

SMILES

O=C1C2=C(SC3=C1C=CC=C3)C=CC=C2

InChI

InChIKey=YRHRIQCWCFGUEQ-UHFFFAOYSA-N
InChI=1S/C13H8OS/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H

HIDE SMILES / InChI

Molecular Formula C13H8OS
Molecular Weight 212.267
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Endocrine-disrupting effects of thioxanthone photoinitiators.
2013-03
Thioxanthone: on the shape of the first absorption band.
2010-08-28
Well-defined PMMA brush on silica particles fabricated by surface-initiated photopolymerization (SIPP).
2010-04
Facile approach to patterned binary polymer brush through photolithography and surface-initiated photopolymerization.
2010-04
Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.
2010-02-01
Theoretical study on reactions of triplet excited state thioxanthone with indole.
2009-11-20
2,4-Diethyl-thioxanthen-9-one.
2009-02-28
A phase I dose-escalation study of SR271425, an intravenously dosed thioxanthone analog, administered weekly in patients with refractory solid tumors.
2009-02
Photoreaction of thioxanthone with indolic and phenolic derivatives of biological relevance: magnetic field effect study.
2008-11-20
Aryl-aryl bond formation by flash vacuum pyrolysis of benzannulated thiopyrans.
2008-07-04
Accessing the triplet excited state in perylenediimides.
2008-03-05
Intramolecular sensitization of photocleavage of the photolabile 2-(2-nitrophenyl)propoxycarbonyl (NPPOC) protecting group: photoproducts and photokinetics of the release of nucleosides.
2008
Structure-retention and mobile phase-retention relationships for reversed-phase high-performance liquid chromatography of several hydroxythioxanthone derivatives in binary acetonitrile-water mixtures.
2007-12-12
On the mechanism of intramolecular sensitization of photocleavage of the 2-(2-nitrophenyl)propoxycarbonyl (NPPOC) protecting group.
2007-10-10
QTc monitoring during a phase I study: experience with SR271425.
2007-04
Novel aldose reductase inhibitors derived from 6-[[(diphenylmethylene)amino]oxy]hexanoic acid.
2007-04
Synthesis of xanthones, thioxanthones, and acridones by the coupling of arynes and substituted benzoates.
2007-01-19
Direct analysis of isopropylthioxanthone (ITX) in milk by high-performance liquid chromatography/tandem mass spectrometry.
2007
Studies on reaction of amino acids and triplet thioxanthone derivatives by laser flash photolysis.
2006-11
The interplay of inverted redox potentials and aromaticity in the oxidized states of new pi-electron donors: 9-(1,3-dithiol-2-ylidene)fluorene and 9-(1,3-dithiol-2-ylidene)thioxanthene derivatives.
2006-04-12
Spectral and photophysical properties of thioxanthone in protic and aprotic solvents: the role of hydrogen bonds in S1-thioxanthone deactivation.
2006-03-13
Novel in vitro model barriers for evaluation of the permeability of antitumor compounds, thioxanthones.
2006-03
A europium complex that selectively stains nucleoli of cells.
2006-02-22
Enhancement of chain amplification in photoreactions of N-methoxypyridinium salts with alcohols.
2005-09-24
Release and report: a new photolabile caging system with a two-photon fluorescence reporting function.
2005-09-14
Bimolecular hydrogen abstraction from phenols by aromatic ketone triplets.
2005-07-27
Singlet exciplexes between a thioxanthone derivative and substituted aromatic quenchers: role of the resonance integral.
2005-03-04
Hydroxy-thioxanthones as suitable neutral ionophores for the preparation of PVC-membrane potentiometric sensors for Al(III) ion.
2004-02
S-pixyl analogues as photocleavable protecting groups for nucleosides.
2002-11-01
High-performance liquid chromatographic method for the estimation of the novel investigational anti-cancer agent SR271425 and its metabolites in mouse plasma.
2001-08-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:13:23 GMT 2025
Edited
by admin
on Mon Mar 31 21:13:23 GMT 2025
Record UNII
EOK1SAC304
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-15912
Preferred Name English
THIOXANTHONE
MI  
Systematic Name English
9-THIOXANTHONE
Systematic Name English
9H-THIOXANTHEN-9-ONE
Systematic Name English
9H-THIOXANTHENE, 9-OXO-
Systematic Name English
THIOXANTHEN-9-ONE
Systematic Name English
THIOXANTHONE [MI]
Common Name English
NSC-658181
Code English
Code System Code Type Description
ECHA (EC/EINECS)
207-749-4
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
MERCK INDEX
m10793
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY Merck Index
CAS
492-22-8
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
WIKIPEDIA
Thioxanthone
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
FDA UNII
EOK1SAC304
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID8060082
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
NSC
15912
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
NSC
658181
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY
PUBCHEM
10295
Created by admin on Mon Mar 31 21:13:23 GMT 2025 , Edited by admin on Mon Mar 31 21:13:23 GMT 2025
PRIMARY