Glutathione Transferase A1-1 Catalyzed Conjugation of Polycyclic Aromatic Hydrocarbon Diol-Epoxides with Glutathione

1996 ◽  
Vol 10 (1-4) ◽  
pp. 51-57 ◽  
Author(s):  
Bengt Jernström ◽  
Bengt Mannervik ◽  
Mario Funk ◽  
Albrecht Seidel
Keyword(s):  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Glutathione Transferase ◽  
Diol Epoxides ◽  
Polycyclic Aromatic

Separation of 32P-labeled 3′,5′-bisphosphate nucleotides of polycyclic aromatic hydrocarbon anti-diol-epoxides and derivatives

1995 ◽  
Vol 710 (1) ◽  
pp. 149-157 ◽  
Author(s):  
De-Jin Zhan ◽  
Diogenes Herreno-Saenz ◽  
Li-Hsueh Chiu ◽  
Linda S. Von Tungeln ◽  
Yu-Sun Wu ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Diol Epoxides ◽  
Polycyclic Aromatic

scholarly journals Immediate Consequences of Cigarette Smoking: Rapid Formation of Polycyclic Aromatic Hydrocarbon Diol Epoxides

2011 ◽  
Vol 24 (2) ◽  
pp. 246-252 ◽  
Author(s):  
Yan Zhong ◽  
Steven G. Carmella ◽  
Pramod Upadhyaya ◽  
J. Bradley Hochalter ◽  
Diane Rauch ◽  
...  
Keyword(s):  
Cigarette Smoking ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Diol Epoxides ◽  
Rapid Formation ◽  
Polycyclic Aromatic

1,1’-Biaceanthrylene and 2,2'-Biaceanthrylene: Models for Linking Larger Polycyclic Aromatic Hydrocarbons via Five-Membered Rings

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Polycyclic Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbon ◽  
Electronic Properties ◽  
Aromatic Hydrocarbons ◽  
Model Systems ◽  
Redox Potentials ◽  
Dimer Model ◽  
Optical And Electronic Properties ◽  
Polycyclic Aromatic

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>

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