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A Potent, Selective and Cell-Active Allosteric Inhibitor of Protein Arginine Methyltransferase 3 (PRMT3).
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 17, p. 5166, doi. 10.1002/anie.201412154
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- Article
Identification of the first in silico-designed TREK1 antagonists that block channel currents dose dependently.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 6, p. 807, doi. 10.1111/cbdd.12810
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- Article
Novel Scaffold Identification of mGlu1 Receptor Negative Allosteric Modulators Using a Hierarchical Virtual Screening Approach.
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- Chemical Biology & Drug Design, 2016, v. 87, n. 2, p. 239, doi. 10.1111/cbdd.12654
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- Article
Tubulin Inhibitor Identification by Bioactive Conformation Alignment Pharmacophore-Guided Virtual Screening.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 5, p. 998, doi. 10.1111/cbdd.12568
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- Article
ESET methylates UBF at K232/254 and regulates nucleolar heterochromatin plasticity and rDNA transcription.
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- Nucleic Acids Research, 2014, v. 42, n. 3, p. 1628, doi. 10.1093/nar/gkt1041
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- Article
Synthesis of 3,4-Dimethylidene Oxacycles through Prins-Type Cyclization of Allenylmethylsilanes.
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- Chemistry - An Asian Journal, 2011, v. 6, n. 8, p. 2092, doi. 10.1002/asia.201100162
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- Article
A Potent, Selective and Cell-Active Allosteric Inhibitor of Protein Arginine Methyltransferase 3 (PRMT3).
- Published in:
- Angewandte Chemie, 2015, v. 127, n. 17, p. 5255, doi. 10.1002/ange.201412154
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- Publication type:
- Article
Palladium‐Catalyzed Carbonylative Coupling Reactions of N,N‐Bis(methanesulfonyl)amides through C–N Bond Cleavage.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 41, p. 5717, doi. 10.1002/ejoc.201801124
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- Article
Identification of highly potent and selective inhibitor, TIPTP, of the p22phox-Rubicon axis as a therapeutic agent for rheumatoid arthritis.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61630-x
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- Article
Metal‐free Synthesis of β‐Nitrostyrenes via DDQ‐Catalyzed Nitration.
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- Bulletin of the Korean Chemical Society, 2021, v. 42, n. 3, p. 525, doi. 10.1002/bkcs.12232
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- Article
Synthesis of N‐Alkyl‐Carbazole Derivatives as 5‐HT<sub>7</sub>R Antagonists.
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- Bulletin of the Korean Chemical Society, 2018, v. 39, n. 9, p. 1083, doi. 10.1002/bkcs.11555
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- Article
Facile Synthesis of 2-Amino-4-alkoxypyrimidines via Consecutive Nucleophilic Aromatic Substitution ( S<sub>N</sub>Ar) Reactions.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 12, p. 1998, doi. 10.1002/bkcs.11014
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- Article
Synthesis and Biological Evaluation of N<sup>3</sup>-Alkyl-Thienopyrimidin-4-Ones as mGluR1 Antagonists.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 5, p. 1439, doi. 10.1002/bkcs.10283
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- Article
In silico probing and biological evaluation of SETDB1/ESET-targeted novel compounds that reduce tri-methylated histone H3K9 (H3K9me3) level.
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- Journal of Computer-Aided Molecular Design, 2017, v. 31, n. 10, p. 877, doi. 10.1007/s10822-017-0052-3
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- Article
Correction: Kim et al. Mito-TIPTP Increases Mitochondrial Function by Repressing the Rubicon-p22phox Interaction in Colitis-Induced Mice. Antioxidants 2021, 10 , 1954.
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- 2023
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- Correction Notice
Mito-TIPTP Increases Mitochondrial Function by Repressing the Rubicon-p22phox Interaction in Colitis-Induced Mice.
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- Antioxidants, 2021, v. 10, n. 12, p. 1954, doi. 10.3390/antiox10121954
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- Article
Synthesis of Benzo[a]quinolizidines via an Aza‐Michael/Oxidative Mannich Process.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 9, p. 1617, doi. 10.1002/ajoc.201900137
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- Article
Remodeling of heterochromatin structure slows neuropathological progression and prolongs survival in an animal model of Huntington's disease.
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- Acta Neuropathologica, 2017, v. 134, n. 5, p. 729, doi. 10.1007/s00401-017-1732-8
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- Article
Single-carbon discrimination by selected peptides for individual detection of volatile organic compounds.
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- Scientific Reports, 2015, p. 9196, doi. 10.1038/srep09196
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- Article
Total Synthesis of Paecilomycine A.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 13, p. 2199, doi. 10.1002/anie.200605058
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- Article
Total Synthesis of Ambruticin.
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- Angewandte Chemie International Edition, 2002, v. 41, n. 1, p. 176, doi. 10.1002/1521-3773(20020104)41:1<176::AID-ANIE176>3.0.CO;2-#
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- Article
Synthesis and Biological Evaluation of Disubstituted Pyrimidines as Selective 5-HT2C Agonists.
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- Molecules, 2019, v. 24, n. 18, p. 3234, doi. 10.3390/molecules24183234
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- Article
Intermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 34, p. 6190, doi. 10.1002/anie.200990178
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- Article
Intermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 12, p. 2196, doi. 10.1002/anie.200804576
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- Article