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Synthesis of spiro[isobenzofuran-1(3H),4'-piperidines] as potential central nervous system agents. 4. Central nervous system depressants
Synthesis and some pharmacological properties of the 23-peptide 15-lysine-secretin-(5-27). Special role of the residue in position 15 in biological activity of the vasoactive intestinal polypeptide
Synthesis and analgesic-antiinflammatory activity of some 4- and 5-substituted heteroarylsalicylic acids
Synthesis, opiate receptor affinity, and conformational parameters of [4-tryptophan]enkephalin analogs
2-(Substituted phenyl)oxazolo[4,5-b]pyridines and 2-(substituted phenyl)oxazolo[5,4-b]pyridines as nonacidic antiinflammatory agents
Potential anticancer agents. 17. Analogs of methotrexate with a tripeptide side chain
Benzopyrones. 14. Synthesis and anti-allergic properties of some N-tetrazolylcarboxamides and related compounds
Synthesis and biological activities of some uronic acids, uronates, uronamides, and urononitriles of pyrimidine nucleosides
Phosphorus-nitrogen compounds. 22. Synthesis and antitumor activity of arylsulfonylhydrazones
Potential bis-alkylating agents for cancer chemotherapy. Approaches to the synthesis of 2-sulfonyl-1,4-bis(dimethanesulfonoxy)butanes
Book Reviews
Synthesis of substituted 1-hydroxy-2-naphthanilides as potential cestodicidal agents
Synthesis and analgetic activity of some benzomorphan analogs
Synthesis and .beta.-adrenoceptor activity of the erythro and threo isomers of substituted .alpha.-hydroxytrimetoquinol
Novel analgesic-antiinflammatory salicylates
Molecular properties of the adrenergic .alpha. receptor. 2. Optimum covalent inhibition by two different prototypes of polyamine disulfides
Three-dimensional mapping of the sweet taste receptor site
Psychotropic agents. 3. 4-(4-Substituted piperidinyl)-1-(4-fluorophenyl)-1-butanones with potent neuroleptic activity
Use of adenine nucleotide derivatives to assess the potential of exo-active-site-directed reagents as species- or isozyme-specific enzyme inactivators. 2. Isozyme-specific inactivation of a mammalian enzyme and its significance in the possible design of fetal isozyme targeted antineoplastic agents
Potential anticancer agents. 16. Methotrexate analogs with a modified peptide side chain
Structure-activity relationships for the inhibition of acrosin by benzamidine derivatives
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