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http://hub.abes.fr/acs/periodical/jmcmar/1986/volume_29/issue_9/101021jm00159a009/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1988/volume_31/issue_12/101021jm00120a009/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1974/volume_17/issue_4/101021jm00250a019/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1969/volume_12/issue_3/101021jm00303a616/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_16/101021jm800400k/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_24/101021jm0580398/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_20/101021jm800461k/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_21/101021jm020188s/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_14/101021jm800250z/authorship/13
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_11/101021jm021113r/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_18/101021jm060605r/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_25/101021jm0408215/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_1/101021jm0110082/authorship/13
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_16/101021jm061487a/authorship/14
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_8/101021jm011066n/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_11/101021jm00173a004/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1975/volume_40/issue_15/101021jo00903a025/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1977/volume_20/issue_3/101021jm00213a016/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27/issue_12/101021jm00378a001/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_11/101021jm00063a002/authorship/2
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Notes. Researches in the Field of Antiviral Compounds. Mannich Bases of 3-Hydroxycoumarin
Cholinergic compounds. 9. Cyclohexane analogs of deoxamuscarine and derivatives
2-[[[2-(2,6-Dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzoxathian: a new antagonist with high potency and selectivity towards .alpha.1-adrenoreceptors
Structure-activity relationships in 1,4-benzodioxan-related compounds. 4. Effect of aryl and alkyl substituents at position 3 on .alpha.-adrenoreceptor blocking activity
Synthesis and identification by shift reagents of isomeric 2-methyl-2-n-propylcyclopentane-1,3-diols
Structure-activity relationships in 1,4-benzodioxan related compounds. 3. 3-Phenyl analogs of 2-[[[2-(2,6-dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzodioxan (WB 4101) as highly selective .alpha.1-adrenoreceptor antagonists
Cyclopentane analog of muscarone
3-[5-(4,5-Dihydro-1H-imidazol-2-yl)-furan-2-yl]phenylamine (Amifuraline), a PromisingReversible and Selective Peripheral MAO-A Inhibitor
Novel Ligands Rationally Designed for Characterizing I2−Imidazoline Binding Sites Nature and Functions
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 7.Selectivity of 4-Phenylchroman Analogues for α1−Adrenoreceptor Subtypes
α2-Adrenoreceptors Profile Modulation. 3. (R)-(+)-m-Nitrobiphenyline, a New Efficient andα2C-Subtype Selective Agonist
α2-Adrenoreceptors Profile Modulation and High Antinociceptive Activity of(S)-(−)-2-[1-(Biphenyl-2-yloxy)ethyl]-4,5-dihydro-1H-imidazole
α2-Adrenoreceptors Profile Modulation. 2. Biphenyline Analogues as Tools forSelective Activation of the α2C-Subtype
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 8.{2-[2-(4-Chlorobenzyloxy)phenoxy]ethyl}-[2-(2,6-dimethoxyphenoxy)ethyl]amine(Clopenphendioxan) as a Tool to Highlight the Involvement of α1D- andα1B-Adrenoreceptor Subtypes in the Regulation of Human PC-3 Prostate CancerCell Apoptosis and Proliferation
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 9. From 1,4-Benzodioxane to 1,4-Dioxane Ring as a Promising Template of Novel α1D-Adrenoreceptor Antagonists, 5-HT1A Full Agonists, and Cytotoxic Agents
α2-Adrenoreceptors Profile Modulation. 4. From Antagonist to Agonist Behavior
Homoazanicotine: A Structure-Affinity Study for Nicotinic Acetylcholine(nACh) Receptor Binding
Imidazoline Binding Sites (IBS) Profile Modulation: Key Role of the Bridge inDetermining I1-IBS or I2-IBS Selectivity within a Series of2-Phenoxymethylimidazoline Analogues
Molecular requirements of the recognition site of cholinergic receptors. 22. Resolution, absolute configuration, and cholinergic enantioselectivity of (+)- and (-)-cis-2-methyl-5-[(dimethylamino)methyl]-1,3-oxathiolane methiodide
Structure-activity relationships in 1,4-benzodioxan-related compounds. Investigation on the role of the dehydrodioxane ring on .alpha.1-adrenoreceptor blocking activity
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