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Details

Stereochemistry ACHIRAL
Molecular Formula C22H14
Molecular Weight 278.3466
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PICENE

SMILES

C1=CC=C2C(C=CC3=C2C=CC4=C3C=CC5=CC=CC=C45)=C1

InChI

InChIKey=GBROPGWFBFCKAG-UHFFFAOYSA-N
InChI=1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H

HIDE SMILES / InChI

Molecular Formula C22H14
Molecular Weight 278.3466
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Electronic absorption spectroscopy of polycyclic aromatic hydrocarbons (PAHs) radical cations generated in oleum: a superacid medium.
2010-12
Superconductivity in alkali-metal-doped picene.
2010-03-04
Sensitivity and bias of molecular marker-based aerosol source apportionment models to small conltibutions of coal combustion soot.
2009-10-15
Air-assisted high-performance field-effect transistor with thin films of picene.
2008-08-13
Characteristics of particulate carbon emissions from real-world Chinese coal combustion.
2008-07-15
ANNINE-6plus, a voltage-sensitive dye with good solubility, strong membrane binding and high sensitivity.
2008-04
Electron-intramolecular-vibration interactions in positively charged phenanthrene-edge-type hydrocarbons.
2004-02-15
Functional characterization of global genomic DNA repair and its implications for cancer.
2003-11
p53 controls global nucleotide excision repair of low levels of structurally diverse benzo(g)chrysene-DNA adducts in human fibroblasts.
2002-09-15
Comparative carcinogenicity of picene and dibenz[a,h]anthracene in the rat.
2002-01-11
Inhibition of gap-junctional intercellular communication by environmentally occurring polycyclic aromatic hydrocarbons.
2002-01
Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study.
2001-02-09
The cytosolic receptor binding affinities and AHH induction potencies of 29 polynuclear aromatic hydrocarbons.
1986-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:04:30 GMT 2025
Edited
by admin
on Mon Mar 31 19:04:30 GMT 2025
Record UNII
F70R8ZBR7T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PICENE
MI  
Systematic Name English
NSC-406006
Preferred Name English
PICENE [IARC]
Common Name English
PICENE [MI]
Common Name English
3,4-BENZCHRYSENE
Common Name English
Code System Code Type Description
MESH
C056699
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-918-7
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
WIKIPEDIA
PICENE
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
PUBCHEM
9162
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
CHEBI
33090
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID8073895
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
FDA UNII
F70R8ZBR7T
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
MERCK INDEX
m8778
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY Merck Index
CAS
213-46-7
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY
NSC
406006
Created by admin on Mon Mar 31 19:04:30 GMT 2025 , Edited by admin on Mon Mar 31 19:04:30 GMT 2025
PRIMARY