Search Results - "Mokrosz, Jerzy L"
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Synthesis and quantitative structure-activity relationship analysis of 2-(aryl or heteroaryl)quinolin-4-amines, a new class of anti-HIV-1 agents
Published in Journal of medicinal chemistry (01-05-1991)“…Thirty-eight 2-(aryl or heteroaryl)quinolin-4-amines, N,N-disubstituted, N-monosubstituted, and without a substituent at the amino group have been synthesized…”
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Binding of unfused aromatic cations to DNA. The influence of molecular twist on intercalation
Published in Journal of the American Chemical Society (01-12-1988)Get full text
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Structure and spectral properties of β-carbolines. 8. Mechanism of the Pictet-Spengler cyclization: An MNDO approach
Published in Tetrahedron (27-02-1995)“…Formation of 1,2,3,4-tetrahydro-β-carboline in the Pictet-Spengler reaction was studied using an MNDO approach. It was shown that the formation of the…”
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8-[4-[2-(1,2,3,4-Tetrahydroisoquinolinyl)]butyl]-8-azaspiro[4.5]decane-7,9-dione: A New 5-HT1A Receptor Ligand with the Same Activity Profile as Buspirone
Published in Journal of medicinal chemistry (01-03-1996)“…A new analog of buspirone (1), i.e., 8-[4-[2-(1,2,3,4-tetrahydroisoquinolinyl)]butyl]-8-azaspiro[4.5]decane-7,9-dione (6a), was synthesized. In was…”
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Stereoelectronic factors in the interaction with DNA of small aromatic molecules substituted with a short cationic chain: Importance of the polarity of the aromatic system of the molecule
Published in Biochemistry (Easton) (10-11-1992)“…We have performed a quantitative analysis of the interaction with DNA of several unfused aromatic compounds synthesized in our laboratory and substituted with…”
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Quantitative structure-activity relationship analysis of cation-substituted polyaromatic compounds as potentiators (amplifiers) of bleomycin-mediated degradation of DNA
Published in Journal of medicinal chemistry (01-02-1991)“…A set of 21 polyheteroaromatic compounds substituted with flexible cationic groups and of similar molecular size has been analyzed for binding with DNA and for…”
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Molecular basis for bleomycin amplification: conformational and stereoelectronic effects in unfused amplifiers
Published in Journal of medicinal chemistry (01-06-1988)“…Sixteen unfused heterobiaromatic and biphenyl compounds substituted with an amino side chain (protonated in water) have been tested for (i) binding with DNA…”
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Synthesis and stereochemistry of new trihydrodiazabicyclo-[3.m.n]alkano[4′,5′:1,2]pyrido[3,4-b]indole ring system
Published in Journal of heterocyclic chemistry (01-12-1993)“…The classical Pictet‐Spengler reaction of tryptamine with the isomeric N‐benzylpiperidones 3a, 3b and N‐benzylpyrrolidone 3c yielded the spiro derivatives of…”
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A biphasic nature of the bleomycin-mediated degradation of DNA
Published in FEBS letters (05-12-1988)“…The bleomycin-mediated digestion of DNA in the presence of ferrous ion, molecular oxygen, and dithiothreitol is characterized by a fast initial reaction, which…”
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Structure-activity relationship studies of central nervous system agents. 13. 4-[3-(Benzotriazol-1-yl)propyl]-1-(2-methoxyphenyl)piperazine, a new putative 5-HT1A receptor antagonist, and its analogs
Published in Journal of medicinal chemistry (19-08-1994)“…A new set of 4-alkyl-1-(o-methoxyphenyl)piperazines containing a terminal benzotriazole fragment were synthesized, and their 5-HT1A and 5-HT2 affinity was…”
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Structure-activity relationship studies of CNS agents--XVII. Spiro[piperidine-4',1-(1,2,3,4-tetrahydro-beta-carboline)] as a probe defining the extended topographic model of 5-HT1A receptors
Published in Bioorganic & medicinal chemistry (01-05-1995)“…Spiro[piperidine-4',1-(1,2,3,4-tetrahydro-beta-carboline)] (10), its derivatives 11-15 and its analogs 16 and 17 were examined as ligands of serotonin 5-HT1A…”
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Structure-activity relationship studies of central nervous system agents. 5. Effect of the hydrocarbon chain on the affinity of 4-substituted 1-(3-chlorophenyl)piperazines for 5-HT1A receptor site
Published in Journal of medicinal chemistry (26-06-1992)“…The effect of the hydrocarbon chain of the model 4-substituted 1-(3-chlorophenyl)piperazines 12-31 on their affinity for 5-HT1A receptor sites was…”
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Structure-activity relationship studies of CNS agents-XVII. Spiro[piperidine-4′,1-(1,2,3,4-tetrahydro-β-carboline)] as a probe defining the extended topographic model of 5-HT 1A receptors
Published in Bioorganic & medicinal chemistry (1995)“…Spiro[piperidine-4′,1-(1,2,3,4-tetrahydro-β-carboline)] ( 10), its derivatives 11–15 and its analogs 16 and 17 were examined as ligands of serotonin 5-HT 1A…”
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3-(omega-Aminoalkyl)-5,5-dialkyl(or spirocycloalkyl-1',5-)hydantoins as new 5-HT1A and 5-HT2A receptor ligands
Published in Archiv der Pharmazie (Weinheim) (01-06-1996)“…A series of new 3-(omega-aminoalkyl)-5,5-disubstituted hydantoins, containing 1-phenylpiperazine, 1-(o-methoxyphenyl)piperazine or…”
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Conformational analysis of 4-(2′-furyl)-2-(methylamino)pyrimidine
Published in Journal of heterocyclic chemistry (01-07-1996)“…Conformational transformations of the title compound 1 were studied using high‐resolution 1H‐nmr techniques, semi‐empirical PM3 calculations and molecular…”
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