Works matching IS 13811991 AND DT 2013 AND VI 17 AND IP 2
Results: 16
Identification of novel Interleukin-2 inhibitors through computational approaches.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 345, doi. 10.1007/s11030-013-9431-4
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Plate-based diversity subset screening: an efficient paradigm for high throughput screening of a large screening file.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 319, doi. 10.1007/s11030-013-9438-x
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Docking of a novel DNA methyltransferase inhibitor identified from high-throughput screening: insights to unveil inhibitors in chemical databases.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 337, doi. 10.1007/s11030-013-9428-z
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Synthesis of novel spirooxindolo-pyrrolidines, pyrrolizidines, and pyrrolothiazoles via a regioselective three-component [3+2] cycloaddition and their preliminary antimicrobial evaluation.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 271, doi. 10.1007/s11030-013-9432-3
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Recent progress in asymmetric Biginelli reaction.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 389, doi. 10.1007/s11030-013-9439-9
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Optimizing lactose hydrolysis by computer-guided modification of the catalytic site of a wild-type enzyme.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 371, doi. 10.1007/s11030-013-9437-y
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One-pot synthesis of tetrazolo[1,5- a]pyrimidines under solvent-free conditions.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 307, doi. 10.1007/s11030-013-9435-0
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- Article
Quinazoline-2,4( $$1H,3H$$)-diones inhibit the growth of multiple human tumor cell lines.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 197, doi. 10.1007/s11030-012-9421-y
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An efficient and expeditious synthesis of novel 2,2-dialkyl-2,3-dihydrobenzofurans from phenols and 2,2-dialkylacetaldehydes.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 261, doi. 10.1007/s11030-013-9429-y
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A simple route for the synthesis of novel $$N$$-alkyl-2-(alkylthio)-1 $$H$$-imidazole derivatives.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 383, doi. 10.1007/s11030-013-9430-5
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Synthesis of novel isoquinolinone and 1,2-dihydroisoquinoline scaffolds via Ugi reaction and ring opening reaction of furans.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 295, doi. 10.1007/s11030-013-9434-1
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Design, synthesis and biological evaluation of indolizine derivatives as HIV-1 VIF-ElonginC interaction inhibitors.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 221, doi. 10.1007/s11030-013-9424-3
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Design of peptide affinity ligands for S-protein: a comparison of combinatorial and de novo design strategies.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 357, doi. 10.1007/s11030-013-9436-z
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One pot three component reaction for the rapid synthesis of pyrrolo[1,2- a]benzimidazoles.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 285, doi. 10.1007/s11030-013-9433-2
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A novel enzyme-catalyzed synthesis of N-substituted pyrrole derivatives.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 245, doi. 10.1007/s11030-013-9426-1
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$$N,N,N^{\prime },N^{\prime }$$-Tetrabromobenzene-1,3-disulfonamide and poly( $$N$$-bromo- $$N$$-ethylbenzene-1,3-disulfonamide) as new and efficient catalysts for the synthesis of highly substituted 1,6-dihydropyrazine-2,3-dicarbonitrile derivatives.
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- Molecular Diversity, 2013, v. 17, n. 2, p. 251, doi. 10.1007/s11030-013-9427-0
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