Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM048722-04S1
Application #
2412205
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1993-01-01
Project End
1997-03-31
Budget Start
1997-01-01
Budget End
1997-03-31
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Wayne State University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
City
Detroit
State
MI
Country
United States
Zip Code
48202
Zhang, Rui; Vanover, Eric; Luo, Weilong et al. (2014) Photochemical generation and kinetic studies of a putative porphyrin-ruthenium(V)-oxo species. Dalton Trans 43:8749-56
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Su, Zhi; Horner, John H; Newcomb, Martin (2012) Rates of fatty acid oxidations by P450 compound I are pH dependent. Chembiochem 13:2061-4
Pan, Zhengzheng; Newcomb, Martin (2011) Acid-catalyzed disproportionation of oxoiron(IV) porphyrins to give oxoiron(IV) porphyrin radical cations. Inorg Chem Commun 14:968-970
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Yuan, Xinting; Sheng, Xin; Horner, John H et al. (2010) Low temperature photo-oxidation of chloroperoxidase Compound II. J Inorg Biochem 104:1156-63
Vanover, Eric; Huang, Yan; Xu, Libin et al. (2010) Photocatalytic aerobic oxidation by a bis-porphyrin-ruthenium(IV) mu-oxo dimer: observation of a putative porphyrin-ruthenium(V)-oxo intermediate. Org Lett 12:2246-9
Sheng, Xin; Zhang, Haoming; Im, Sang-Choul et al. (2009) Kinetics of oxidation of benzphetamine by compounds I of cytochrome P450 2B4 and its mutants. J Am Chem Soc 131:2971-6
Harischandra, Dilusha N; Lowery, Gerald; Zhang, Rui et al. (2009) Production of a putative iron(V)-oxocorrole species by photo-disproportionation of a bis-corrole-diiron(IV)-mu-oxo dimer: implication for a green oxidation catalyst. Org Lett 11:2089-92
Yuan, Xinting; Wang, Qin; Horner, John H et al. (2009) Kinetics and activation parameters for oxidations of styrene by Compounds I from the cytochrome P450(BM-3) (CYP102A1) heme domain and from CYP119. Biochemistry 48:9140-6

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