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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_9/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_9/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	9
Rights Holder	American Chemical Society
is Is Part Of of	Property-Based Design: Optimization of Drug Absorption andPharmacokinetics Azepanone-Based Inhibitors of Human and Rat Cathepsin K Structure-Based Approach for the Discovery of Bis-benzamidines as NovelInhibitors of Matriptase Antitumor Agents. 207. Design, Synthesis, and Biological Testing of4β-Anilino-2-fluoro-4‘-demethylpodophyllotoxin Analogues as Cytotoxic andAntiviral Agents Short Peptides with Induced β-Turn Inhibit the Interaction between HIV-1gp120 and CD4 Indenopyrazoles as Novel CyclinDependent Kinase (CDK) Inhibitors Antitumor Benzothiazoles. 14. Synthesis and in Vitro Biological Properties ofFluorinated 2-(4-Aminophenyl)benzothiazoles Atropisomeric Derivatives of2‘,6‘-Disubstituted(R)-11-Phenylaporphine: SelectiveSerotonin 5-HT7 Receptor Antagonists Novel Seco Cyclopropa[c]pyrrolo[3,2-e]indole Bisalkylators Bearing a3,3‘-Arylenebisacryloyl Group as a Linker Design, Synthesis, and Discovery of a Novel CCR1 Antagonist Development of Potent Truncated Glucagon Antagonists Effect of N-Alkyl and N-Alkenyl Substituents in Noroxymorphindole,17-Substituted-6,7-dehydro-4,5α-epoxy-3,14-dihydroxy-6,7:2‘,3‘-indolomorphinans,on Opioid Receptor Affinity, Selectivity, and Efficacy Novel Peptide Conjugates for Tumor-Specific Chemotherapy Bisubstrate Analogue Inhibitors of 6-Hydroxymethyl-7,8-dihydropterinPyrophosphokinase: Synthesis and Biochemical and Crystallographic Studies N-Methyl Scan of Somatostatin Octapeptide Agonists Produces InterestingEffects on Receptor Subtype Specificity Discovery of Novel N-Phenylglycine Derivatives as Potent and Selectiveβ3-Adrenoceptor Agonists for the Treatment of Frequent Urination and UrinaryIncontinence Synthesis and Structural Studies of Aza Analogues of Functionalized AminoAcids: New Anticonvulsant Agents Efficient Preparations of the β-Glucuronides of Dihydroartemisinin andStructural Confirmation of the Human Glucuronide Metabolite Dicationic Bis(9-methylphenazine-1-carboxamides): Relationships betweenBiological Activity and Linker Chain Structure for a Series of PotentTopoisomerase Targeted Anticancer Drugs (4-Piperidin-1-yl)phenyl Amides: Potent and Selective Human β3 Agonists

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