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Woster Patrick M.
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http://hub.abes.fr/acs/periodical/jmcmar/1986/volume_29/issue_5/101021jm00155a045/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/101021jm0505009/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_6/101021jm00126a026/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_1/101021jm000084m/authorship/2
http://hub.abes.fr/oup/periodical/carcin/2007/volume_28/issue_11/101093carcinbgm162/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_8/101021jm980603/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_13/101021jm000188x/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_16/101021jm040096y/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_24/101021jm010111o/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_8/101021jm701384x/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_10/101021jm058203r/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/1989/volume_28/issue_21/101021bi00447a026/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1992/volume_35/issue_17/101021jm00095a015/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_20/101021jm00072a020/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_10/101021jm00010a021/authorship/5
http://hub.abes.fr/springer/periodical/280/1995/volume_36/issue_1/B956F395708F0ADFE053120B220AAD6A/authorship/6
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S-(5'-Deoxy-5'-adenosyl)-1-ammonio-4-(methylsulfonio)-2-cyclopentene: a potent, enzyme-activated irreversible inhibitor of S-adenosylmethionine decarboxylase
S-(5'-Deoxy-5'-adenosyl)-1-aminoxy-4-(methylsulfonio)-2-cyclopentene (AdoMao): An Irreversible Inhibitor of S-Adenosylmethionine Decarboxylase with Potent in Vitro Antitrypanosomal Activity
Synthesis and biological evaluation of S-adenosyl-1,12-diamino-3-thio-9-azadodecane, a multisubstrate adduct inhibitor of spermine synthase
Studies of the mechanism by which increased spermidine/spermine N1-acetyltransferase activity increases susceptibility to skin carcinogenesis
1-(N-Alkylamino)-11-(N-ethylamino)-4,8-diazaundecanes: Simple SyntheticPolyamine Analogues That Differentially Alter Tubulin Polymerization
Fundamentals of Medicinal Chemistry By GarethThomas. John Wiley and Sons, Ltd., West Sussex, U.K..2003. xv + 285 pp. 19 × 24.5 cm. ISBN 0-4708-4307-1.$30.00.
Polyaminohydroxamic Acids and Polyaminobenzamides as Isoform Selective Histone Deacetylase Inhibitors
Alkyl-Substituted Polyaminohydroxamic Acids: A Novel Class of TargetedHistone Deacetylase Inhibitors
Writing Reaction Mechanisms in Organic Chemistry, Second Edition By Audrey Miller and PhilippaH. Solomon. Harcourt Academic Press, New York. 2000.xiv + 471 pp. 19 x 23.5 cm. ISBN 0-12- 496712-4. $48.50.
Terminally Alkylated Polyamine Analogues as Chemotherapeutic Agents
Solid Phase Synthesis. Edited by Kevin Burgess.Wiley Interscience, New York. 2000. xiv + 277 pp. 15.5× 23.5 cm. ISBN 0471318256. $69.95.
Science of Synthesis: Houben−Weyl Methods ofMolecular Transformation Georg Thieme Verlag,Stuttgart, Germany. 2005. 41627 pp. URL: http://www.science-of-synthesis.com (Electronic Version, 48Volumes). Price Based on Web Site and Number ofUsers.
Effect of S-adenosyl-1,12-diamino-3-thio-9-azadodecane, a multisubstrate adduct inhibitor of spermine synthase, on polyamine metabolism in mammalian cells
Synthesis and biological evaluation of cyclic analogs of l-carnitine as potential agents in the treatment of myocardial ischemia
Growth and biochemical effects of unsymmetrically substituted polyamine analogues in human lung tumor cells 1
Synthesis and evaluation of unsymmetrically substituted polyamine analogs as modulators of human spermidine/spermine-N1-acetyltransferase (SSAT) and as potential antitumor agents
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