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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1991/volume_34
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1991/volume_34/issue_12/m/web http://hub.abes.fr/acs/periodical/jmcmar/1991/volume_34/issue_12/m/print
issue	12
is Is Part Of of	Antitumor agents. 120. New 4-substituted benzylamine and benzyl ether derivatives of 4'-O-demethylepipodophyllotoxin as potent inhibitors of human DNA topoisomerase II (.+-.)-3-Allyl-6-bromo-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine, a new high affinity D1 dopamine receptor ligand: synthesis and structure-activity relationship Examination of HIV-1 protease secondary structure specificity using conformationally constrained inhibitors Editorial - The Journal of Medicinal Chemistry Becomes a Biweekly Publication in 1992 Immunostimulation by a partially modified retro-inverso-tuftsin analog containing Thr1.sum..psi.[NHCO](R,S)Lys2 modification 1,3,8-Trisubstituted xanthines. Effects of substitution pattern upon adenosine receptor A1/A2 affinity [Erratum to document cited in CA114(19):185119j] Stereospecific synthesis of (R)- and (S)-S-adenosyl-1,8-diamino-3-thiooctane, a potent inhibitor of polyamine biosynthesis. Comparison of asymmetric induction vs enantiomeric synthesis [Erratum to document cited in CA115(5):50181y] Masthead Synthesis and antibacterial activities of C-21 functionalized derivatives of (9R)-9-amino-9-deoxoerythromycins A and B Book Reviews Molecular mechanics simulations on covalent complexes of mitomycin C and its analogs with left-handed DNA duplexes Novel alkaloids from the tropical plant Ancistrocladus abbreviatus inhibit cell killing by HIV-1 and HIV-2 Cholecystokinin (CCK) antagonists: (R)-tryptophan-based hybrid antagonists of high affinity and selectivity for CCK-A receptors Synthesis and resolution of (.+-.)-7-chloro-8-hydroxy-1-(3'-iodophenyl)-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (TISCH): a high affinity and selective iodinated ligand for CNS D1 dopamine receptor [Erratum to document cited in CA114(13):122017d] Novel 1-phenylpiperazine and 4-phenylpiperidine derivatives as high-affinity .sigma. ligands Activity of N6-substituted 2-chloroadenosines at A1 and A2 adenosine receptors Delineating the pharmacophoric elements of huperzine A: importance of the unsaturated three-carbon bridge to its AChE inhibitory activity

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