H E MAY
Overview
Explore the profile of H E MAY including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
94
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Recent Articles
1.
Briscoe W, Anderson S, MAY H
Biochem Pharmacol
. 1990 Sep;
40(6):1201-9.
PMID: 2403375
Chemical modifications of guanine are some of the most common results of interactions of DNA with many carcinogens and anti-cancer drugs, including nitrosoureas, nitrogen mustards, triazenes, polycyclic aromatics, and aflatoxins....
2.
Mercer L, MAY H, Dodds S
J Nutr
. 1989 Oct;
119(10):1465-71.
PMID: 2511286
The Saturation Kinetics Model (SKM) is useful in describing many physiological responses as functions of a limiting dietary nutrient. However, as nutrients are fed at higher dietary concentrations, responses become...
3.
Kohlhepp S, MAY H, Reed D
Drug Metab Dispos
. 1981 Mar;
9(2):135-41.
PMID: 6113112
Urinary metabolites of ring 14C-labeled 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) and 1-(2-chloroethyl)-3-(trans-4-methylcyclohexyl)-1-nitrosourea (Methyl CCNU) from rats have been isolated and characterized by high-performance liquid chromatography and mass spectrometry. About 44% of the cyclohexyl...
4.
MAY H, Kohlhepp S, BOOSE R, Reed D
Cancer Res
. 1979 Mar;
39(3):762-72.
PMID: 427763
Liver microsomal metabolism of 1-(2-chloroethyl)-3-(trans-4-methylcyclohexyl)-1-nitrosourea in the presence of reduced nicotinamide adenine dinucleotide phosphate and O2 was shown to produce seven metabolites that included the parent urea. A cytochrome P-450-dependent...
5.
MAY H, Boose R, Reed D
Biochemistry
. 1975 Oct;
14(21):4723-30.
PMID: 1182112
Liver microsomal hydroxylation of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea was shown to occur on the cyclohexyl ring at positions 3 and 4. Four metabolites were isolated by selective solvent extraction and purifed by high-pressure...
6.
7.
Reed D, MAY H, BOOSE R, Gregory K, Beilstein M
Cancer Res
. 1975 Mar;
35(3):568-76.
PMID: 1116123
Chemical degradation of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea or 1-(2-chloroethyl)-3-(trans-4-methylcyclohexyl)-1-nitrosourea in buffer under physiological conditions resulted in the formation of a significant quantity of 2-chlorethanol (18 to 25% of the initial nitrosourea concentration). Other...
8.
MAY H, Boose R, Reed D
Biochem Biophys Res Commun
. 1974 Mar;
57(2):426-33.
PMID: 4151402
No abstract available.
9.
10.
MCCAY P, Poyer J, Pfeifer P, MAY H, Gilliam J
Lipids
. 1971 May;
6(5):297-306.
PMID: 4397359
No abstract available.