Biology-oriented synthesis of a tetrahydroisoquinoline-based compound collection targeting microtubule polymerization. - Wikidata - wikimedia - TriplyDB

Biology-oriented synthesis of a tetrahydroisoquinoline-based compound collection targeting microtubule polymerization.

Biology-oriented synthesis of a tetrahydroisoquinoline-based compound collection targeting microtubule polymerization.

http://www.wikidata.org/entity/Q39201808

about

Composition and applications of focus libraries to phenotypic assays EDL-360: A Potential Novel Antiglioma Agent.High content screening of diverse compound libraries identifies potent modulators of tubulin dynamics.Tetrahydroisoquinolines: New Inhibitors of Neutrophil Extracellular Trap (NET) Formation.Enantioselective Organocatalytic Synthesis of a Secoyohimbane-Inspired Compound Collection with Neuritogenic Activity.Scaffold Diversity Synthesis and Its Application in Probe and Drug Discovery.Synthesis of a novel polycyclic ring scaffold with antimitotic properties via a selective domino Heck-Suzuki reaction.Synthesis of the B-seco limonoid core scaffold.Drug design based on pentaerythritol tetranitrate reductase: synthesis and antibacterial activity of Pogostone derivatives.A general catalytic reaction sequence to access alkaloid-inspired indole polycycles Catalytic Aerobic Oxidation and Tandem Enantioselective Cycloaddition in Cascade Multicomponent Synthesis

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P2860

Biology-oriented synthesis of a tetrahydroisoquinoline-based compound collection targeting microtubule polymerization.

http://www.wikidata.org/entity/Q39201808

description

2013 nî lūn-bûn

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name

Biology-oriented synthesis of ...... ng microtubule polymerization.

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Biology-oriented synthesis of ...... ng microtubule polymerization.

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Biology-oriented synthesis of ...... ng microtubule polymerization.

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Christian Hedberg

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Nancy E Martinez

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Sayantani Roy

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Slava Ziegler

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Tobias J Zimmermann

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P2860

Tubulin-interactive natural products as anticancer agents

Microtubule-binding agents: a dynamic field of cancer therapeutics.

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

Bioactivity-guided navigation of chemical space.

A novel microtubule-modulating noscapinoid triggers apoptosis by inducing spindle multipolarity via centrosome amplification and declustering.

Biology-inspired synthesis of compound libraries.

Taccalonolides: Novel microtubule stabilizers with clinical potential.

A novel microtubule-modulating agent induces mitochondrially driven caspase-dependent apoptosis via mitotic checkpoint activation in human prostate cancer cells.

New microtubule polymerization inhibitors comprising a nitrooxymethylphenyl group.

Biology-oriented synthesis.

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295-300

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scholarly article

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10.1002/CBIC.201200711

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3

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14

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Herbert Waldmann

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2013-01-31T00:00:00Z

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23364933

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