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Chemical Biology of Epothilones.
- Published in:
- Angewandte Chemie International Edition, 1998, v. 37, n. 15, p. 2014, doi. 10.1002/(SICI)1521-3773(19980817)37:15<2014::AID-ANIE2014>3.0.CO;2-2
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- Article
Synthesis and Biological Activity of Sarcodictyins.
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- Angewandte Chemie International Edition, 1998, v. 37, n. 10, p. 1418, doi. 10.1002/(SICI)1521-3773(19980605)37:10<1418::AID-ANIE1418>3.0.CO;2-5
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- Article
Total Synthesis of Epothilone E and Analogues with Modified Side Chains through the Stille Coupling Reaction.
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- Angewandte Chemie International Edition, 1998, v. 37, n. 1/2, p. 84, doi. 10.1002/(SICI)1521-3773(19980202)37:1/2<84::AID-ANIE84>3.0.CO;2-V
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- Article
Total Synthesis of Eleutherobin.
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- Angewandte Chemie International Edition, 1997, v. 36, n. 22, p. 2520, doi. 10.1002/anie.199725201
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- Article
Designed Epothilones: Combinatorial Synthesis, Tubulin Assembly Properties, abd Cytotoxic Action against Taxol-Resistant Tumor Cells.
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- Angewandte Chemie International Edition, 1997, v. 36, n. 19, p. 2097, doi. 10.1002/anie.199720971
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- Article
Total Synthesis of Epothilone A: The Olefin Metathesis Approach.
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- Angewandte Chemie International Edition, 1997, v. 36, n. 1/2, p. 166, doi. 10.1002/anie.199701661
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- Article
An Approach to Epothilones Based on Olefin Metathesis.
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- Angewandte Chemie International Edition, 1996, v. 35, n. 20, p. 2399, doi. 10.1002/anie.199623991
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- Article
Molecular Recognition by Glycoside Pseudo Base Pairs and Triples in an Apramycin–RNA ComplexThis work was supported by the National Institutes of Health (Grant no. AI51104 to T.H.).
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- Angewandte Chemie, 2005, v. 117, n. 18, p. 2754, doi. 10.1002/ange.200500028
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- Article
Monitoring Molecular Recognition of the Ribosomal Decoding SiteS.S. and Q.Z. contributed equally. This work was supported in part by the National Institutes of Health (Grant AI51104 to T.H.). We are grateful to Prof. Yitzhak Tor, University of California, San Diego, for helpful discussions and suggestions that initiated our interest in using 2-aminopurine as a fluorescence label.
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- Angewandte Chemie, 2004, v. 116, n. 24, p. 3239, doi. 10.1002/ange.200454217
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- Article
Antitumor efficacy of 26-fluoroepothilone B against human prostate cancer xenografts.
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- 2001
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- Publication type:
- journal article
Total Synthesis of Oxazole- and Cyclopropane-Containing Epothilone B Analogues by the Macrolactonization Approach.
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- Chemistry - A European Journal, 1997, v. 3, n. 12, p. 1971, doi. 10.1002/chem.19970031212
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- Article
Total Synthesis of Oxazole- and Cyclopropane-Containing Epothilone A Analogues by the Olefin Metathesis Approach.
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- Chemistry - A European Journal, 1997, v. 3, n. 12, p. 1957, doi. 10.1002/chem.19970031211
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- Article
Synthesis and Biopharmaceutical Evaluation of Imatinib Analogues Featuring Unusual Structural Motifs.
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- ChemMedChem, 2016, v. 11, n. 1, p. 31, doi. 10.1002/cmdc.201500510
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- Article
Conformational dynamics of the EGFR kinase domain reveals structural features involved in activation.
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- Proteins, 2009, v. 76, n. 2, p. 375, doi. 10.1002/prot.22353
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- Article
A Zebrafish In Vivo Phenotypic Assay to Identify 3-Aminothiophene-2-Carboxylic Acid-Based Angiogenesis Inhibitors.
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- Assay & Drug Development Technologies, 2014, v. 12, n. 9/10, p. 527, doi. 10.1089/adt.2014.606
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- Article
Synthesis of 5,6-Spiroethers and Evaluation of their Affinities for the Bacterial A Site.
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- ChemBioChem, 2011, v. 12, n. 8, p. 1188, doi. 10.1002/cbic.201100076
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- Article
Designed Spiro-Bicyclic Analogues Targeting the Ribosomal Decoding Center.
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- ChemBioChem, 2011, v. 12, n. 1, p. 71, doi. 10.1002/cbic.201000591
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- Article
Unnatural Rigid Scaffolds Targeting the Bacterial Ribosome.
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- ChemBioChem, 2009, v. 10, n. 12, p. 1969, doi. 10.1002/cbic.200900268
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- Article
Aminoglycoside-Hybrid Ligands Targeting the Ribosomal Decoding Site.
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- ChemBioChem, 2005, v. 6, n. 1, p. 58, doi. 10.1002/cbic.200400197
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- Article
Piperidine Glycosides Targeting the Ribosomal Decoding Site.
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- ChemBioChem, 2003, v. 4, n. 9, p. 886, doi. 10.1002/cbic.200300689
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- Article
Novel Acyclic Deoxystreptamine Mimetics Targeting the Ribosomal Decoding Site.
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- ChemBioChem, 2003, v. 4, n. 9, p. 879, doi. 10.1002/cbic.200300688
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- Article
Novel Paromamine Derivatives Exploring Shallow-Groove Recognition of Ribosomal- Decoding-Site RNA.
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- ChemBioChem, 2002, v. 3, n. 12, p. 1223, doi. 10.1002/1439-7633(20021202)3:12<1223::AID-CBIC1223>3.0.CO;2-W
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- Publication type:
- Article
Molecular Recognition by Glycoside Pseudo Base Pairs and Triples in an Apramycin–RNA ComplexThis work was supported by the National Institutes of Health (Grant no. AI51104 to T.H.).
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 18, p. 2694, doi. 10.1002/anie.200500028
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- Publication type:
- Article
Monitoring Molecular Recognition of the Ribosomal Decoding SiteS.S. and Q.Z. contributed equally. This work was supported in part by the National Institutes of Health (Grant AI51104 to T.H.). We are grateful to Prof. Yitzhak Tor, University of California, San Diego, for helpful discussions and suggestions that initiated our interest in using 2-aminopurine as a fluorescence label.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 24, p. 3177, doi. 10.1002/anie.200454217
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- Publication type:
- Article
The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century.
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- Angewandte Chemie International Edition, 2000, v. 39, n. 1, p. 44, doi. 10.1002/(SICI)1521-3773(20000103)39:1<44::AID-ANIE44>3.0.CO;2-L
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- Article