Journal of the American Chemical Society

Carcinogenic Hydrocarbons. V. A Comparison of the Fluorescence Intensity of Cholanthrene and Certain of its Homologs1

WF Bruce

Index: Bruce Journal of the American Chemical Society, 1941 , vol. 63, p. 301

Full Text: HTML

Citation Number: 7

Abstract

A preliminary study of the relative fluorescence intensities of some of the homologs of cholanthrene has shown a diminution of fluorescence intensity as the series is ascended. 2 In that study numerically equal concentrations of the hydrocarbons were fortuitously employed. By using equimolecular concentrations, we now find that the higher members of the series are nearly alike in fluorescence intensity, although a slight diminution with ...

Related Articles:

Two classes of p38α MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes

[Michelotti, Enrique L.; Moffett, Kristofer K.; Nguyen, Duyan; Kelly, Martha J.; Shetty, Rupa; Chai, Xiaomei; Northrop, Katrina; Namboodiri, Variketta; Campbell, Brandon; Flynn, Gary A.; Fujimoto, Ted; Hollinger, Frank P.; Bukhtiyarova, Marina; Springman, Eric B.; Karpusas, Michael Bioorganic and Medicinal Chemistry Letters, 2005 , vol. 15, # 23 p. 5274 - 5279]

Macrocyclic inhibitors of penicillopepsin. 1. Design, synthesis, and evaluation of an inhibitor bridged between P1 and P3

[Gruber, Rene; Cagniant, Denise; Cagniant, Paul Bulletin de la Societe Chimique de France, 1983 , vol. 2, # 3-4 p. 96 - 104]

Macrocyclic inhibitors of penicillopepsin. 1. Design, synthesis, and evaluation of an inhibitor bridged between P1 and P3

[Gruber, Rene; Cagniant, Denise; Cagniant, Paul Bulletin de la Societe Chimique de France, 1983 , vol. 2, # 3-4 p. 96 - 104]

Macrocyclic inhibitors of penicillopepsin. 1. Design, synthesis, and evaluation of an inhibitor bridged between P1 and P3

[Gruber, Rene; Cagniant, Denise; Cagniant, Paul Bulletin de la Societe Chimique de France, 1983 , vol. 2, # 3-4 p. 96 - 104]

More Articles...