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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10O2
Molecular Weight 222.2387
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLANTHRAQUINONE

SMILES

CC1=CC=C2C(=O)C3=C(C=CC=C3)C(=O)C2=C1

InChI

InChIKey=NJWGQARXZDRHCD-UHFFFAOYSA-N
InChI=1S/C15H10O2/c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16/h2-8H,1H3

HIDE SMILES / InChI

Molecular Formula C15H10O2
Molecular Weight 222.2387
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Activation of aryl hydrocarbon receptor signaling by extracts of teak and other wood dusts.
2015-12
Lactones and quinones from the tubers of Sinningia aggregata.
2010-08-27
Naphthoquinones and anthraquinones from scent glands of a dyspnoid Harvestman, Paranemastoma quadripunctatum.
2010-02
2-methylanthraquinone as a marker of occupational exposure to teak wood dust in boatyards.
2009-01
Positive and negative aspects of soda/anthraquinone pulping of hardwoods.
2008-11
Investigation of Indian diospyros species for antiplasmodial properties.
2008-06
Larvicidal activity of tectoquinone isolated from red heartwood-type Cryptomeria japonica against two mosquito species.
2008-06
2-(4-Methyl-benzo-yl)benzoic acid monohydrate.
2008-04-23
Anthraquinones from the roots of Prismatomeris malayana.
2008
Activity of quinones from teak (Tectona grandis) on fungal cell wall stress.
2006-08
Newbouldiaquinone A: A naphthoquinone-anthraquinone ether coupled pigment, as a potential antimicrobial and antimalarial agent from Newbouldia laevis.
2006-03
[Studies on the chemical constituents from stem of Chirita longgangensis var. Hongyao].
2006-02
Newbouldiaquinone and newbouldiamide: a new naphthoquinone-anthraquinone coupled pigment and a new ceramide from Newbouldia laevis.
2005-06
Antitermitic quinones from Diospyros sylvatica.
2004-05
Development of a sequential supercritical fluid extraction method for the analysis of nitrated and oxygenated derivatives of polycyclic aromatic hydrocarbons in urban aerosols.
2003-08-29
Nanosecond time-resolved studies of long-lived photoinduced charge separation in the dyad fluorescein-anthraquinone-methyl ester adsorbed on TiO2 colloids.
2003-07-15
New pyranonaphthoquinone and pyranonaphthohydroquinone from the roots of Pentas longiflora.
2002-09
Differential inhibition of HIV-1 preintegration complexes and purified integrase protein by small molecules.
1996-09-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:56:40 GMT 2025
Edited
by admin
on Mon Mar 31 18:56:40 GMT 2025
Record UNII
Q9P233HWAJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-607
Preferred Name English
2-METHYLANTHRAQUINONE
MI  
Systematic Name English
2-METHYLANTHRAQUINONE [MI]
Common Name English
2-METHYL-9,10-ANTHRACENEDIONE
Systematic Name English
METHYLANTHRAQUINONE, 2-
Systematic Name English
.BETA.-METHYLANTHRAQUINONE
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 252200
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
Code System Code Type Description
MERCK INDEX
m7365
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY Merck Index
NSC
607
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
WIKIPEDIA
2-Methylanthraquinone
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
PUBCHEM
6773
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID5041439
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
CHEBI
9427
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
FDA UNII
Q9P233HWAJ
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
CAS
84-54-8
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
MESH
C073955
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-539-6
Created by admin on Mon Mar 31 18:56:40 GMT 2025 , Edited by admin on Mon Mar 31 18:56:40 GMT 2025
PRIMARY