Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H12O |
| Molecular Weight | 244.2873 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC2=C(C=CC3=C2C=CC=C3)C4=CC=CC=C14
InChI
InChIKey=VXFDOYXVHRYCGS-UHFFFAOYSA-N
InChI=1S/C18H12O/c19-18-11-17-13-6-2-1-5-12(13)9-10-15(17)14-7-3-4-8-16(14)18/h1-11,19H
| Molecular Formula | C18H12O |
| Molecular Weight | 244.2873 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Urinary profiles to assess polycyclic aromatic hydrocarbons exposure in coke-oven workers. | 2010-01-15 |
|
| Urinary polycyclic aromatic hydrocarbons and monohydroxy metabolites as biomarkers of exposure in coke oven workers. | 2009-08 |
|
| Using gold nanoparticles to improve the recovery and the limits of detection for the analysis of monohydroxy-polycyclic aromatic hydrocarbons in urine samples. | 2009-07-31 |
|
| Using liquid chromatography-tandem mass spectrometry to quantify monohydroxylated metabolites of polycyclic aromatic hydrocarbons in urine. | 2009-04-15 |
|
| Development of a gas chromatography/mass spectrometry method to quantify several urinary monohydroxy metabolites of polycyclic aromatic hydrocarbons in occupationally exposed subjects. | 2008-11-15 |
|
| Urinary hydroxylated metabolites of polycyclic aromatic hydrocarbons as biomarkers of exposure in asphalt workers. | 2007-04-25 |
|
| Quantitative determination of de-conjugated chrysene metabolites in fish bile by HPLC-fluorescence and GC--MS. | 2004-02 |
|
| Determination of selected monohydroxy metabolites of 2-, 3- and 4-ring polycyclic aromatic hydrocarbons in urine by solid-phase microextraction and isotope dilution gas chromatography-mass spectrometry. | 2002-10-05 |
|
| Relative potencies of individual polycyclic aromatic hydrocarbons to induce dioxinlike and estrogenic responses in three cell lines. | 2002 |
|
| Several synthetic chemicals inhibit progesterone receptor-mediated transactivation in yeast. | 1997-04-07 |
|
| Formation of mono- and diglucuronides and other glycosides of benzo(a)pyrene-3,6-quinol by V79 cell-expressed human phenol UDP-glucuronosyltransferases of the UGT1 gene complex. | 1995-05-26 |
|
| Mono- and diglucuronide formation from chrysene and benzo(a)pyrene phenols by 3-methylcholanthrene-inducible phenol UDP-glucuronosyltransferase (UGT1A1). | 1992-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:00:45 GMT 2025
by
admin
on
Mon Mar 31 22:00:45 GMT 2025
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| Record UNII |
9CRJ4NM6HV
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| Record Status |
Validated (UNII)
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| Record Version |
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IN-VIVO
URINE
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