| Year |
Citation |
Score |
| 2013 |
Cowan EA, Taylor JL, Oldham CD, Dasari M, Doyle D, Murthy N, May SW. Cellular antioxidant activity of phenylaminoethyl selenides as monitored by chemiluminescence of peroxalate nanoparticles and by reduction of lipopolysaccharide-induced oxidative stress. Enzyme and Microbial Technology. 53: 373-7. PMID 24315639 DOI: 10.1016/J.Enzmictec.2013.08.002 |
0.669 |
|
| 2012 |
Kang JY, Costyn LJ, Nagy T, Cowan EA, Oldham CD, May SW, Arnold RD. Abstract 2751: Protective effects of phenylaminoethyl selenide (PAESe) on doxorubicin-induced cardiotoxicityin vitroandin vivo Cancer Research. 72: 2751-2751. DOI: 10.1158/1538-7445.Am2012-2751 |
0.669 |
|
| 2011 |
Kang JY, Costyn LJ, Nagy T, Cowan EA, Oldham CD, May SW, Arnold RD. The antioxidant phenylaminoethyl selenide reduces doxorubicin-induced cardiotoxicity in a xenograft model of human prostate cancer. Archives of Biochemistry and Biophysics. 515: 112-9. PMID 21906582 DOI: 10.1016/J.Abb.2011.08.008 |
0.665 |
|
| 2011 |
Cowan EA, Oldham CD, May SW. Identification of a thioselenurane intermediate in the reaction between phenylaminoalkyl selenoxides and glutathione. Archives of Biochemistry and Biophysics. 506: 201-7. PMID 21081105 DOI: 10.1016/J.Abb.2010.11.007 |
0.674 |
|
| 2011 |
Foster MS, Oldham CD, May SW. Looking glass mechanism-based inhibition of peptidylglycine α-amidating monooxygenase Tetrahedron Asymmetry. 22: 283-293. DOI: 10.1016/J.Tetasy.2011.01.006 |
0.336 |
|
| 2007 |
Bauer JD, Sunman JA, Foster MS, Thompson JR, Ogonowski AA, Cutler SJ, May SW, Pollock SH. Anti-inflammatory effects of 4-phenyl-3-butenoic acid and 5-(acetylamino)-4-oxo-6-phenyl-2-hexenoic acid methyl ester, potential inhibitors of neuropeptide bioactivation. The Journal of Pharmacology and Experimental Therapeutics. 320: 1171-7. PMID 17138865 DOI: 10.1124/Jpet.106.110940 |
0.325 |
|
| 2007 |
Burns KL, Oldham CD, Thompson JR, Lubarsky M, May SW. Analysis of the in vitro biocatalytic production of poly-(β)-hydroxybutyric acid Enzyme and Microbial Technology. 41: 591-599. DOI: 10.1016/J.Enzmictec.2007.05.003 |
0.325 |
|
| 2007 |
Bauer JD, Foster MS, Hugdahl JD, Burns KL, May SW, Pollock SH, Cutler HG, Cutler SJ. Synthesis and pharmacological evaluation of m-terphenyl amines as cyclooxygenase inhibitors Medicinal Chemistry Research. 16: 119-129. DOI: 10.1007/S00044-007-9015-X |
0.306 |
|
| 2005 |
Burns KL, Gelbaum LT, Sullards MC, Bostwick DE, May SW. Iso-coenzyme A. The Journal of Biological Chemistry. 280: 16550-8. PMID 15708855 DOI: 10.1074/Jbc.M411898200 |
0.363 |
|
| 2004 |
De Silva V, Woznichak MM, Burns KL, Grant KB, May SW. Selenium redox cycling in the protective effects of organoselenides against oxidant-induced DNA damage. Journal of the American Chemical Society. 126: 2409-13. PMID 14982447 DOI: 10.1021/Ja037294J |
0.332 |
|
| 2003 |
Burns KL, May SW. Separation methods applicable to the evaluation of enzyme-inhibitor and enzyme-substrate interactions. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 797: 175-90. PMID 14630149 DOI: 10.1016/J.Jchromb.2003.08.038 |
0.314 |
|
| 2003 |
McIninch JK, McIninch JD, May SW. Catalysis, stereochemistry, and inhibition of ureidoglycolate lyase. The Journal of Biological Chemistry. 278: 50091-100. PMID 14506266 DOI: 10.1074/Jbc.M303828200 |
0.351 |
|
| 2002 |
May SW. Selenium-based pharmacological agents: an update. Expert Opinion On Investigational Drugs. 11: 1261-9. PMID 12225247 DOI: 10.1517/13543784.11.9.1261 |
0.334 |
|
| 2001 |
Overcast JD, Ensley AE, Buccafusco CJ, Cundy C, Broadnax RA, He S, Yoganathan AP, Pollock SH, Hartley CJ, May SW. Evaluation of cardiovascular parameters of a selenium-based antihypertensive using pulsed Doppler ultrasound. Journal of Cardiovascular Pharmacology. 38: 337-46. PMID 11486238 DOI: 10.1097/00005344-200109000-00002 |
0.705 |
|
| 2000 |
Feng J, Shi J, Sirimanne SR, Mounier-Lee CE, May SW. Kinetic and stereochemical studies on novel inactivators of C-terminal amidation. The Biochemical Journal. 350: 521-30. PMID 10947967 DOI: 10.1042/Bj3500521 |
0.351 |
|
| 2000 |
Woznichak MM, Overcast JD, Robertson K, Neumann HM, May SW. Reaction of phenylaminoethyl selenides with peroxynitrite and hydrogen peroxide. Archives of Biochemistry and Biophysics. 379: 314-20. PMID 10898950 DOI: 10.1006/Abbi.2000.1893 |
0.731 |
|
| 1999 |
May SW. Applications of oxidoreductases Current Opinion in Biotechnology. 10: 370-375. PMID 10449319 DOI: 10.1016/S0958-1669(99)80067-6 |
0.32 |
|
| 1999 |
Moore AB, May SW. Kinetic and inhibition studies on substrate channelling in the bifunctional enzyme catalysing C-terminal amidation. The Biochemical Journal. 341: 33-40. PMID 10377242 DOI: 10.1042/Bj3410033 |
0.333 |
|
| 1999 |
May SW. Selenium-based drug design: Rationale and therapeutic potential Expert Opinion On Investigational Drugs. 8: 1017-1030. DOI: 10.1517/13543784.8.7.1017 |
0.339 |
|
| 1998 |
May SW, Pollock SH. Selenium-based antihypertensives. Rationale and potential Drugs. 56: 959-964. PMID 9878985 DOI: 10.2165/00003495-199856060-00001 |
0.373 |
|
| 1997 |
Mounier CE, Shi J, Sirimanne SR, Chen BH, Moore AB, Gill-Woznichak MM, Ping D, May SW. Pyruvate-extended amino acid derivatives as highly potent inhibitors of carboxyl-terminal peptide amidation. The Journal of Biological Chemistry. 272: 5016-23. PMID 9030564 DOI: 10.1074/Jbc.272.8.5016 |
0.346 |
|
| 1997 |
Wonznirhak MM, Ogonowski AA, Wang L, Overcast JD, Smith JH, Hrowner RV, Pollock SH, May SW. Biochemistry and pharmacology of novel selenium compounds Faseb Journal. 11: A1152. |
0.746 |
|
| 1996 |
May SW, Young FK, Powers JL, Gill-Woznichak MM. Mechanism-based inactivation of dopamine beta-monooxygenase in adrenal chromaffin cells. Biochemical and Biophysical Research Communications. 228: 278-84. PMID 8920906 DOI: 10.1006/Bbrc.1996.1653 |
0.356 |
|
| 1995 |
Sirimanne SR, May SW. Interaction of non-conjugated olefinic substrate analogues with dopamine beta-monooxygenase: catalysis and mechanism-based inhibition. The Biochemical Journal. 306: 77-85. PMID 7864832 DOI: 10.1042/Bj3060077 |
0.414 |
|
| 1995 |
Ping D, Mounier CE, May SW. Reaction versus subsite stereospecificity of peptidylglycine α- monooxygenase and peptidylamidoglycolate lyase, the two enzymes involved in peptide amidation Journal of Biological Chemistry. 270: 29250-29255. PMID 7493955 DOI: 10.1074/Jbc.270.49.29250 |
0.31 |
|
| 1995 |
Wimalasena K, May SW. Ascorbic acid mediated N-dealkylation and N-deoxygenation of N,N'-dimethylaniline N-oxide Journal of the American Chemical Society. 117: 2381-2386. DOI: 10.1021/Ja00114A001 |
0.638 |
|
| 1994 |
Li C, Oldham CD, May SW. NN-Dimethyl-1,4-phenylenediamine as an alternative reductant for peptidylglycine α-amidating mono-oxygenase catalysis Biochemical Journal. 300: 31-36. PMID 8198547 DOI: 10.1042/Bj3000031 |
0.378 |
|
| 1992 |
Debnath J, Husain PA, May SW. Activation of an adrenergic pro-drug through sequential stereoselective action of tandem target enzymes Biochemical and Biophysical Research Communications. 189: 33-39. PMID 1449487 DOI: 10.1016/0006-291X(92)91521-Q |
0.315 |
|
| 1991 |
Katopodis AG, Ping D, Smith CE, May SW. Functional and structural characterization of peptidylamidoglycolate lyase, the enzyme catalyzing the second step in peptide amidation Biochemistry. 30: 6189-6194. PMID 2059626 DOI: 10.1021/Bi00239A016 |
0.335 |
|
| 1991 |
Herman HH, Husain PA, Colbert JE, Schweri MM, Pollock SH, Fowler LC, May SW. The enantiomeric specificity of the antihypertensive activity of 1-(phenylthio)-2-aminopropane, a synthetic substrate analogue for dopamine β-monooxygenase Journal of Medicinal Chemistry. 34: 1082-1085. PMID 2002450 DOI: 10.1021/Jm00107A031 |
0.365 |
|
| 1990 |
Katopodis AG, May SW. Novel substrates and inhibitors of peptidylglycine alpha-amidating monooxygenase. Biochemistry. 29: 4541-4548. PMID 2372538 DOI: 10.1021/Bi00471A006 |
0.348 |
|
| 1990 |
Katopodis AG, Ping D, May SW. A novel enzyme from bovine neurointermediate pituitary catalyzes dealkylation of α-hydroxyglycine derivatives, thereby functioning sequentially with peptidylglycine α-amidating monooxygenase in peptide amidation Biochemistry. 29: 6115-6120. PMID 2207061 DOI: 10.1021/Bi00478A001 |
0.341 |
|
| 1989 |
Wimalasena K, Herman HH, May SW. Effects of dopamine beta-monooxygenase substrate analogs on ascorbate levels and norepinephrine synthesis in adrenal chromaffin granule ghosts. The Journal of Biological Chemistry. 264: 124-30. PMID 2909510 |
0.656 |
|
| 1989 |
Husain PA, Colbert JE, Sirimanne SR, VanDerveer DG, Herman HH, May SW. N-succinimidyl methoxyphenylacetic acid ester, an amine-directed chiral derivatizing reagent suitable for enzymatic scale resolutions. Analytical Biochemistry. 178: 177-83. PMID 2729571 DOI: 10.1016/0003-2697(89)90376-X |
0.337 |
|
| 1989 |
Wimalasena K, May SW. Dopamine .beta.-monooxygenase-catalyzed aromatization of 1-(2-aminoethyl)-1,4-cyclohexadiene: redirection of specificity and evidence for a hydrogen-atom-transfer mechanism Journal of the American Chemical Society. 111: 2729-2731. DOI: 10.1021/Ja00189A065 |
0.656 |
|
| 1989 |
WIMALASENA K, MAY SW. ChemInform Abstract: Dopamine β-Monooxygenase Catalyzed Aromatization of 1-(2-Aminoethyl)-1,4-cyclohexadiene: Redirection of Specificity and Evidence for a Hydrogen Atom Transfer Mechanism. Cheminform. 20. DOI: 10.1002/chin.198929076 |
0.629 |
|
| 1988 |
May SW, Wimalasena K, Herman HH, Fowler LC, Ciccarello MC, Pollock SH. Novel antihypertensives targeted at dopamine beta-monooxygenase: turnover-dependent cofactor depletion by phenyl aminoethyl selenide. Journal of Medicinal Chemistry. 31: 1066-8. PMID 3373481 DOI: 10.1021/Jm00401A003 |
0.634 |
|
| 1988 |
Katopodis AG, May SW. A new facile trinitrophenylated substrate for peptide α-amidation and its use to characterize PAM activity in chromaffin granules Biochemical and Biophysical Research Communications. 151: 499-505. PMID 3348792 DOI: 10.1016/0006-291X(88)90621-3 |
0.335 |
|
| 1988 |
Herman HH, Wimalasena K, Fowler LC, Beard CA, May SW. Demonstration of the ascorbate dependence of membrane-bound dopamine beta-monooxygenase in adrenal chromaffin granule ghosts. The Journal of Biological Chemistry. 263: 666-72. PMID 3335518 |
0.638 |
|
| 1988 |
Herman HH, Pollock SH, Fowler LC, May SW. Demonstration of the potent antihypertensive activity of phenyl-2-aminoethyl sulfides Journal of Cardiovascular Pharmacology. 11: 501-510. PMID 2455835 DOI: 10.1097/00005344-198805000-00001 |
0.361 |
|
| 1988 |
Sirimanne SR, May SW. Facile stereoselective allylic hydroxylation by dopamine .beta.-monooxygenase Journal of the American Chemical Society. 110: 7560-7561. DOI: 10.1021/Ja00230A059 |
0.301 |
|
| 1987 |
Sirimanne SR, Herman HH, May SW. Interaction of dopamine beta-mono-oxygenase with substituted imidazoles and pyrazoles. Catalysis and inhibition. The Biochemical Journal. 242: 227-33. PMID 3593236 DOI: 10.1042/Bj2420227 |
0.394 |
|
| 1987 |
May SW, Herman HH, Roberts SF, Ciccarello MC. Ascorbate depletion as a consequence of product recycling during dopamine beta-monooxygenase catalyzed selenoxidation. Biochemistry. 26: 1626-1633. PMID 3036204 DOI: 10.1021/Bi00380A021 |
0.399 |
|
| 1987 |
Wimalasena K, May SW. Mechanistic studies on dopamine .beta.-monooxygenase catalysis: N-dealkylation and mechanism-based inhibition by benzylic-nitrogen-containing compounds. Evidence for a single-electron-transfer mechanism Journal of the American Chemical Society. 109: 4036-4046. DOI: 10.1021/Ja00247A033 |
0.669 |
|
| 1987 |
WIMALASENA K, MAY SW. ChemInform Abstract: Mechanistic Studies on Dopamine β-Monooxygenase Catalysis: N-Dealkylation and Mechanism-Based Inhibition by Benzylic-Nitrogen-Containing Compounds. Evidence for a Single-Electron-Transfer Mechanism. Cheminform. 18. DOI: 10.1002/chin.198743348 |
0.644 |
|
| 1986 |
May SW, Katopodis AG. Oxygenation of alcohol and sulphide substrates by a prototypical non-haem iron monooxygenase: catalysis and biotechnological potential Enzyme and Microbial Technology. 8: 17-21. DOI: 10.1016/0141-0229(86)90004-9 |
0.375 |
|
| 1985 |
Padgette SR, Wimalasena K, Herman HH, Sirimanne SR, May SW. Olefin oxygenation and N-dealkylation by dopamine beta-monooxygenase: catalysis and mechanism-based inhibition. Biochemistry. 24: 5826-39. PMID 4084493 DOI: 10.1021/Bi00342A021 |
0.695 |
|
| 1985 |
KATOPODIS AG, WIMALASENA K, LEE J, MAY SW. ChemInform Abstract: MECHANISTIC STUDIES ON NON-HEME IRON MONOOXYGENASE CATALYSIS: EPOXIDATION, ALDEHYDE FORMATION AND DEMETHYLATION BY THE Ω-HYDROXYLATION SYSTEM OF PSEUDOMONAS OLEOVORANS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198515102 |
0.64 |
|
| 1985 |
Padgette SR, Herman HH, Han JH, Pollock SH, May SW. ANTIHYPERTENSIVE ACTIVITIES OF PHENYL AMINOETHYL SULFIDES, A CLASS OF SYNTHETIC SUBSTRATES FOR DOPAMINE β-HYDROXYLASE Cheminform. 16. DOI: 10.1002/Chin.198509180 |
0.329 |
|
| 1984 |
Padgette SR, Herman HH, Han JH, Pollock SH, May SW. Antihypertensive activities of phenyl aminoethyl sulfides, a class of synthetic substrates for dopamine beta-hydroxylase. Journal of Medicinal Chemistry. 27: 1354-1357. PMID 6481771 DOI: 10.1021/Jm00376A024 |
0.347 |
|
| 1984 |
Katopodis AG, Wimalasena K, Lee J, May SW. Mechanistic studies on non-heme iron monooxygenase catalysis: epoxidation, aldehyde formation and demethylation by the .omega.-hydroxylation system of Pseudomonas oleovorans Journal of the American Chemical Society. 106: 7928-7935. DOI: 10.1021/Ja00337A049 |
0.638 |
|
| 1984 |
May SW, Lee LG, Katopodis AG, Kuo JY, Wimalasena K, Thowsen JR. Rubredoxin from Pseudomonas oleovorans: effects of selective chemical modification and metal substitution Biochemistry. 23: 2187-2192. DOI: 10.1021/Bi00305A013 |
0.616 |
|
| 1983 |
May SW, Mueller PW, Padgette SR, Herman HH, Phillips RS. Dopamine-B-hydroxylase: suicide inhibition by the novel olefinic substrate, 1-phenyl-1-aminomethylethene. Biochemical and Biophysical Research Communications. 110: 161-168. PMID 6860408 DOI: 10.1016/0006-291X(83)91274-3 |
0.338 |
|
| 1983 |
Herman HH, Pollock SH, Padgette SR, Lange JR, Han JH, May SW. Effects of phenyl-2-aminoethyl sulfide, a novel dopamine-beta-hydroxylase substrate, on the cardiovascular system of the anesthetized dog. Journal of Cardiovascular Pharmacology. 5: 725-730. PMID 6195457 DOI: 10.1097/00005344-198309000-00004 |
0.367 |
|
| 1983 |
May SW, Padgette SR. Oxidoreductase Enzymes in Biotechnology: Current Status and Future Potential Nature Biotechnology. 1: 677-686. DOI: 10.1038/Nbt1083-677 |
0.326 |
|
| 1983 |
May SW, Mueller PW, Oldham CD, Williamson CK, Sowell AL. Protocatechuate 3,4-dioxygenase: comparative study of inhibition and active-site interactions of pyridine N-oxides Biochemistry. 22: 5331-5340. DOI: 10.1021/Bi00292A012 |
0.301 |
|
| 1982 |
May SW, Phillips RS, Herman HH, Mueller PW. Bioactivation of Cathaedulis alkaloids: Enzymatic ketonization of norpseudoephedrine Biochemical and Biophysical Research Communications. 104: 38-44. PMID 7073680 DOI: 10.1016/0006-291X(82)91937-4 |
0.374 |
|
| 1981 |
Phillips RS, May SW. Enzymatic sulphur oxygenation reactions Enzyme and Microbial Technology. 3: 9-18. DOI: 10.1016/0141-0229(81)90028-4 |
0.335 |
|
| 1980 |
May SW, PRS. Asymmetric sulfoxidation by dopamine .beta.-hydroxylase, an oxygenase heretofore considered specific for methylene hydroxylation Journal of the American Chemical Society. 102: 5981-5983. DOI: 10.1021/Ja00538A080 |
0.308 |
|
| 1979 |
May SW. Enzymatic epoxidation reactions Enzyme and Microbial Technology. 1: 15-22. DOI: 10.1016/0141-0229(79)90005-X |
0.344 |
|
| 1978 |
May SW. Preparation and properties of cobalt(II) rubredoxint Biochemistry. 17: 3333-3338. PMID 687587 DOI: 10.1021/Bi00609A025 |
0.314 |
|
| 1975 |
May SW, Schwartz RD, Abbott BJ, Zaborsky OR. Structural effects on the reactivity of substrates and inhibitors in the epoxidation system of Pseudomonas oleovorans. Biochimica Et Biophysica Acta. 403: 245-55. PMID 1174548 DOI: 10.1016/0005-2744(75)90026-1 |
0.375 |
|
| 1974 |
May SW, Schwartz RD. Stereoselective epoxidation of octadiene catalyzed by an enzyme system of Pseudomonas oleovorans. Journal of the American Chemical Society. 96: 4031-2. PMID 4854399 DOI: 10.1021/Ja00819A060 |
0.304 |
|
| 1974 |
May SW, Schwartz RD. Stereoselective Epoxidation Of Octadiene Catalyzed By An Enzyme System Of Pseudomonas Oleovorans Cheminform. 5. DOI: 10.1002/Chin.197433227 |
0.304 |
|
| 1972 |
May SW, Kaiser ET. On the mechanism of the pepsin-catalyzed hydrolysis of sulfite esters. Biochemistry. 11: 592-600. PMID 4334907 DOI: 10.1021/BI00754A018 |
0.469 |
|
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