Found: 10
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In silico structure‐based design of GABA<sub>B</sub> receptor agonists using a combination of docking and QSAR.
- Published in:
- Chemical Biology & Drug Design, 2019, v. 94, n. 4, p. 1782, doi. 10.1111/cbdd.13580
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- Article
QSAR and Molecular Docking Studies of the Inhibitory Activity of Novel Heterocyclic GABA Analogues over GABA-AT.
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- Molecules, 2018, v. 23, n. 11, p. 2984, doi. 10.3390/molecules23112984
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- Article
Novel-Substituted Heterocyclic GABA Analogues. Enzymatic Activity against the GABA-AT Enzyme from Pseudomonas fluorescens and In Silico Molecular Modeling.
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- Molecules, 2018, v. 23, n. 5, p. 1128, doi. 10.3390/molecules23051128
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- Article
Synthesis of cis- and trans-3-Aminocyclohexanols by Reduction of β-Enaminoketones.
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- Molecules, 2012, v. 17, n. 1, p. 151, doi. 10.3390/molecules17010151
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- Article
Microwave-Assisted Improved Synthesis of Oxazolidin-2-ones, Oxazolidine-2-thiones and Thiazolidine-2-thione Chiral Auxiliaries.
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- Molecules, 2011, v. 16, n. 10, p. 8803, doi. 10.3390/molecules16108803
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- Article
Preclinical safety evaluation of amphotericin A21: A novel antifungal.
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- Basic & Clinical Pharmacology & Toxicology, 2021, v. 129, n. 1, p. 72, doi. 10.1111/bcpt.13592
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- Article
An Amphotericin B Derivative Equally Potent to Amphotericin B and with Increased Safety.
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- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162171
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- Article
1,4‐Disubstituted‐1,2,3‐triazole GABA Analogues: Synthesis, In Vitro Evaluation, Quantum QSAR and Molecular Docking against Pseudomonas fluorescens GABA‐AT.
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- ChemistrySelect, 2020, v. 5, n. 3, p. 1071, doi. 10.1002/slct.201901485
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- Article
Toxicological evaluation of amphotericin B and its synthetic analogue in mice.
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- FASEB Journal, 2007, v. 21, n. 5, p. A441, doi. 10.1096/fasebj.21.5.a441
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- Article
Diasteroselective conjugate addition of diethylaluminum cyanide to a conjugated N-enoyl system: an alternative synthesis of ( S)-pregabalin.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 1, p. 45, doi. 10.1139/cjc-2013-0397
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- Article