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http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_16/101021jm00016a010/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_9/101021jm021118o/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_9/101021jm040894o/authorship/7
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_13/101021jo050362v/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_24/101021jm020940p/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_19/101021jm030878b/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_15/101021jm0580205/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_12/101021jm031126k/authorship/10
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_16/101021ja015550r/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27/issue_12/101021jm00378a009/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_4/101021jm00166a018/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_2/101021jm00122a021/authorship/1
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Synthesis and biological evaluation of 14-alkoxymorphinans. 1. Highly potent opioid agonists in the series of (-)-14-methoxy-N-methylmorphinan-6-ones
Synthesis and biological evaluation of 14-alkoxymorphinans. 2. (-)-N-(Cyclopropylmethyl)-4,14-dimethoxymorphinan-6-one, a selective .mu. opioid receptor antagonist
Effect of a 6-Cyano Substituent in 14-Oxygenated N-Methylmorphinans onOpioid Receptor Binding and Antinociceptive Potency
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 22. Influence ofthe 14-Alkoxy Group and the Substitution in Position 5 in14-Alkoxymorphinan-6-ones on in Vitro and in Vivo Activities
Mechanistic Diversity of the van LeusenReaction Applied to 6-Ketomorphinans andSynthetic Potential of the ResultingAcrylonitrile Substructures
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 18. N-Substituted14-Phenylpropyloxymorphinan-6-ones with Unanticipated Agonist Properties: Extending the Scope of Common Structure−Activity Relationships
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 17. Highly δOpioid Receptor Selective 14-Alkoxy-Substituted Indolo- andBenzofuromorphinans
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 20.14-Phenylpropoxymetopon: An Extremely Powerful Analgesic
Novel Class of Morphinans with AcrylonitrileIncorporated Substructures as Key Intermediates forNon-Oxygen-Bridged Opioid Ligands
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 21. Novel4-Alkoxy and 14-Phenylpropoxy Derivatives of the μ Opioid ReceptorAntagonist Cyprodime
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 11. 3-Hydroxycyprodime and Analogs: Opioid Antagonist Profile in Comparison to Cyprodime
Synthesis and biological evaluation of 14-alkoxymorphinans. 3. Extensive study on cyprodime-related compounds
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