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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_17/m/print http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_17/m/web
Date Copyrighted	1998
Rights	Copyright © 1998 American Chemical Society
issue	17
Rights Holder	American Chemical Society
is Is Part Of of	2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N-methylamide (SDZ NKT 343), a Potent Human NK1 Tachykinin ReceptorAntagonist with Good Oral Analgesic Activity in Chronic Pain Models Structure−Activity Relationships and Molecular Modeling of3,5-Diacyl-2,4-dialkylpyridine Derivatives as Selective A3 Adenosine ReceptorAntagonists Peptidomimetic Growth Hormone Secretagogues. Design Considerations andTherapeutic Potential Synthesis and Comparison of the Antiinflammatory Activity of Manoalide andCacospongionolide B Analogues 2-Substituted Aminopyrido[2,3-d]pyrimidin-7(8H)-ones. Structure−ActivityRelationships Against Selected Tyrosine Kinases and in Vitro and in VivoAnticancer Activity Design and Synthesis of a Series of Potent and Orally Bioavailable NoncovalentThrombin Inhibitors That Utilize Nonbasic Groups in the P1 Position Studies on Quinazolines and 1,2,4-Benzothiadiazine 1,1-Dioxides. 8.,Synthesis and Pharmacological Evaluation of Tricyclic Fused Quinazolines and1,2,4-Benzothiadiazine 1,1-Dioxides as Potential α1-Adrenoceptor Antagonists Syntheses and Structure−Activity Relationships of Novel Retinoid X ReceptorAgonists Synthesis and Pharmacological Evaluation of N,N‘-Diarylguanidines as PotentSodium Channel Blockers and Anticonvulsant Agents Tolerance in the Replacement of the Benzhydrylic O Atom in4-[2-(Diphenylmethoxy)ethyl]-1-benzylpiperidine Derivatives by an N Atom: Development of New-Generation Potent and Selective N-Analogue Molecules forthe Dopamine Transporter 1,4- and 2,6-Disubstituted Amidoanthracene-9,10-dione Derivatives as Inhibitorsof Human Telomerase Design, Synthesis, and Anticonvulsant Activity of1-(Pyrid-3-ylsulfonamido)-2-nitroethylenes Salicylhydrazine-Containing Inhibitors of HIV-1 Integrase: Implication for aSelective Chelation in the Integrase Active Site New Substituted 1,4-Benzoxazine Derivatives with Potential IntracellularCalcium Activity Pyrrolidine-3-carboxylic Acids as Endothelin Antagonists. 3. Discovery of aPotent, 2-Nonaryl, Highly Selective ETA Antagonist (A-216546) Synthesis and Pharmacological Characterization of O-Alkynyloximes ofTropinone and N-Methylpiperidinone as Muscarinic Agonists Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl,2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives ofAdenosine-5‘-N-ethyluronamide as A1 and A3 Adenosine Receptor Agonists

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