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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=CC2=C(C=C1)C3=C(C=C2)C4=C(C=C3)C5=C(C=CC=C5)C=C4

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
The cytosolic receptor binding affinities and AHH induction potencies of 29 polynuclear aromatic hydrocarbons.
1986 Nov
Substituent effects and charge delocalization mode in chrysenium, benzo[c]phenanthrenium, and benzo[g]chrysenium cations: a stable ion and electrophilic substitution study.
2001 Feb 9
Inhibition of gap-junctional intercellular communication by environmentally occurring polycyclic aromatic hydrocarbons.
2002 Jan
Comparative carcinogenicity of picene and dibenz[a,h]anthracene in the rat.
2002 Jan 11
p53 controls global nucleotide excision repair of low levels of structurally diverse benzo(g)chrysene-DNA adducts in human fibroblasts.
2002 Sep 15
Functional characterization of global genomic DNA repair and its implications for cancer.
2003 Nov
Electron-intramolecular-vibration interactions in positively charged phenanthrene-edge-type hydrocarbons.
2004 Feb 15
ANNINE-6plus, a voltage-sensitive dye with good solubility, strong membrane binding and high sensitivity.
2008 Apr
Air-assisted high-performance field-effect transistor with thin films of picene.
2008 Aug 13
Characteristics of particulate carbon emissions from real-world Chinese coal combustion.
2008 Jul 15
Sensitivity and bias of molecular marker-based aerosol source apportionment models to small conltibutions of coal combustion soot.
2009 Oct 15
Electronic absorption spectroscopy of polycyclic aromatic hydrocarbons (PAHs) radical cations generated in oleum: a superacid medium.
2010 Dec
Superconductivity in alkali-metal-doped picene.
2010 Mar 4
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:08:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:08:27 GMT 2023
Record UNII
F70R8ZBR7T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PICENE
MI  
Systematic Name English
PICENE [IARC]
Common Name English
NSC-406006
Code English
PICENE [MI]
Common Name English
3,4-BENZCHRYSENE
Common Name English
Code System Code Type Description
MESH
C056699
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-918-7
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
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WIKIPEDIA
PICENE
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
PUBCHEM
9162
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
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CHEBI
33090
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
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EPA CompTox
DTXSID8073895
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
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FDA UNII
F70R8ZBR7T
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
MERCK INDEX
m8778
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY Merck Index
CAS
213-46-7
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY
NSC
406006
Created by admin on Fri Dec 15 18:08:27 GMT 2023 , Edited by admin on Fri Dec 15 18:08:27 GMT 2023
PRIMARY