Rates of Fatty Acid Oxidations by P450 Compound I are pH Dependent.
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- ChemBioChem, 2012, v. 13, n. 14, p. 2061, doi. 10.1002/cbic.201200387
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- Article
Works matching AU Newcomb, Martin
Results: 10
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Induction of apoptosis in macrophages by Pseudomonas aeruginosa azurin: tumour-suppressor protein p53 and reactive oxygen species, but not redox activity, as critical elements in cytotoxicity.
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- Molecular Microbiology, 2003, v. 47, n. 2, p. 549, doi. 10.1046/j.1365-2958.2003.03317.x
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- Publication type:
- Article
3
An Improved Synthesis of 4-Cycloheptene-1-Carboxylic Acid.
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- Synthetic Communications, 1988, v. 18, n. 11, p. 1193, doi. 10.1080/00397918808060910
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- Article
4
Laser Flash Photolysis Generation and Kinetic Studies of Corrole–Manganese(v)-Oxo Intermediates.
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- Chemistry - A European Journal, 2005, v. 11, n. 19, p. 5713, doi. 10.1002/chem.200500134
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- Article
5
Rate-Controlling Isomerizations in Fatty Acid Oxidations by a Cytochrome P450 Compound I.
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- Chemistry - A European Journal, 2012, v. 18, n. 9, p. 2472, doi. 10.1002/chem.201103170
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- Article
6
Hepatic intra-arterial adriamycin in metastatic leiomyosarcoma: Exploiting the steep dose-response curve.
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- Journal of Surgical Oncology, 1987, v. 36, n. 1, p. 76, doi. 10.1002/jso.2930360118
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- Article
7
Cytochrome P450 119 Compounds I Formed by Chemical Oxidation and Photooxidation Are the Same Species.
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- Chemistry - A European Journal, 2019, v. 25, n. 61, p. 14015, doi. 10.1002/chem.201202254
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- Article
8
(ω-2,ω-2,ω-3,ω-3)-Tetradeuterio-fatty acids for mechanistic studies of enzyme-catalyzed hydroxylation reactions.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2012, v. 55, n. 11, p. 406, doi. 10.1002/jlcr.2959
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- Article
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Products from solvolysis reactions that form (2-phenylcyclopropyl)carbinyl cations.
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- Journal of Physical Organic Chemistry, 2005, v. 18, n. 9, p. 974, doi. 10.1002/poc.951
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- Article
10
Rate constants for ring openings of 2-phenylcyclobutylcarbinyl radicals.
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- Journal of Physical Organic Chemistry, 2000, v. 13, n. 11, p. 688, doi. 10.1002/1099-1395(200011)13:11<688::AID-POC302>3.0.CO;2-J
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