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Details

Stereochemistry ACHIRAL
Molecular Formula C17H12
Molecular Weight 216.2772
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-METHYLPYRENE

SMILES

CC1=CC=C2C=CC3=C4C(C=CC1=C24)=CC=C3

InChI

InChIKey=KBSPJIWZDWBDGM-UHFFFAOYSA-N
InChI=1S/C17H12/c1-11-5-6-14-8-7-12-3-2-4-13-9-10-15(11)17(14)16(12)13/h2-10H,1H3

HIDE SMILES / InChI

Molecular Formula C17H12
Molecular Weight 216.2772
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of sulfotransferase forms involved in the metabolic activation of the genotoxicant 1-hydroxymethylpyrene using bacterially expressed enzymes and genetically modified mouse models.
2014-06-16
Cytokine release and cytotoxicity in human keratinocytes induced by polycyclic aromatic hydrocarbons (1-methylpyrene and perylene).
2010
Fluorescence quenching properties of multiple pyrene-modified RNAs.
2009-07-15
Pyrenylmethyldeoxyadenosine: a 3'-cap for universal DNA hybridization probes.
2009
Time course of hepatic 1-methylpyrene DNA adducts in rats determined by isotope dilution LC-MS/MS and 32P-postlabeling.
2008-10
Pyrene-perylene as a FRET pair coupled to the N2'-functionality of 2'-amino-LNA.
2008-01-01
Efficient quenching of the excimer fluorescence derived from pyrene arrays on RNA duplexes.
2008
Structure-activity investigations of polyamine-anthracene conjugates and their uptake via the polyamine transporter.
2007-08
Pyrene aromatic arrays on RNA duplexes as helical templates.
2007-06-21
Differential utilization of pyrene as the sole source of carbon by Bacillus subtilis and Pseudomonas aeruginosa strains: role of biosurfactants in enhancing bioavailability.
2007-01
Uptake of chemically reactive, DNA-damaging sulfuric acid esters into renal cells by human organic anion transporters.
2006-05
N1-substituent effects in the selective delivery of polyamine conjugates into cells containing active polyamine transporters.
2004-11-18
Defining the molecular requirements for the selective delivery of polyamine conjugates into cells containing active polyamine transporters.
2003-11-20
Pyrenemethyl ara-uridine-2'-carbamate: a strong interstrand excimer in the major groove of a DNA duplex.
2003-09-05
Selective attachment of pyrenyl groups to ethylene-co-vinyl acetate copolymers: dynamic and static fluorescence studies.
2002-09
Fluorometric sensing of alkaline Earth metal cations by new lariat ethers having plural pyrenylmethyl groups on the electron-donating sidearms.
2002-08-08
A double-decker silver(I) coordination polymer of 1-methylpyrene with columnar aromatic stacks. Effect of substituting groups on structure of silver(I) complexes with polycyclic aromatic hydrocarbons.
2001-12-31
[Reagents for modification of protein-nucleic complexes. III. Site-specific photomodification of elongation complex of DNA polymerase beta with arylazide derivatives of primers sensitized with fluorescent ATP gamma-amide].
2001-10-20
Boronic acid fluorophore/beta-cyclodextrin complex sensors for selective sugar recognition in water.
2001-04-01
Three-way analysis of fluorescence spectra of polycyclic aromatic hydrocarbons with quenching by nitromethane.
2001-04-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:14 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:14 GMT 2025
Record UNII
AB8420OXQA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-90776
Preferred Name English
1-METHYLPYRENE
HSDB  
Systematic Name English
3-METHYLPYRENE
Systematic Name English
PYRENE, 1-METHYL-
Systematic Name English
1-METHYLPYRENE [HSDB]
Common Name English
Code System Code Type Description
CAS
2381-21-7
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
NSC
90776
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-178-8
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
PUBCHEM
16932
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
EPA CompTox
DTXSID0025654
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
FDA UNII
AB8420OXQA
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
HSDB
2162
Created by admin on Mon Mar 31 19:15:14 GMT 2025 , Edited by admin on Mon Mar 31 19:15:14 GMT 2025
PRIMARY
Related Record Type Details
METABOLITE -> PARENT