 Chemistry Techniques, Synthetic
"Chemistry Techniques, Synthetic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Methods used for the chemical synthesis of compounds. Included under this heading are laboratory methods used to synthesize a variety of chemicals and drugs.
| Descriptor ID |
D060326
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| MeSH Number(s) |
E05.916.039 G02.607.750.155 J01.897.836.249
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| Concept/Terms |
Chemistry Techniques, Synthetic- Chemistry Techniques, Synthetic
- Chemistry Technique, Synthetic
- Synthetic Chemistry Technique
- Technique, Synthetic Chemistry
- Techniques, Synthetic Chemistry
- Synthetic Chemistry Techniques
Inorganic Synthesis Techniques- Inorganic Synthesis Techniques
- Inorganic Synthesis Technique
- Synthesis Technique, Inorganic
- Synthesis Techniques, Inorganic
- Technique, Inorganic Synthesis
- Techniques, Inorganic Synthesis
- Methods of Inorganic Synthesis
- Inorganic Synthesis Methods
- Inorganic Synthesis Method
- Method, Inorganic Synthesis
- Methods, Inorganic Synthesis
- Synthesis Method, Inorganic
- Synthesis Methods, Inorganic
Peptide Synthesis, Synthetic- Peptide Synthesis, Synthetic
- Peptide Syntheses, Synthetic
- Syntheses, Synthetic Peptide
- Synthesis, Synthetic Peptide
- Synthetic Peptide Syntheses
- Synthetic Peptide Synthesis
Organic Synthesis Techniques- Organic Synthesis Techniques
- Organic Synthesis Technique
- Synthesis Technique, Organic
- Synthesis Techniques, Organic
- Technique, Organic Synthesis
- Techniques, Organic Synthesis
- Organic Synthesis Methods
- Method, Organic Synthesis
- Methods, Organic Synthesis
- Methods of Organic Synthesis
Peptide Synthesis Techniques- Peptide Synthesis Techniques
- Peptide Synthesis Technique
- Synthesis Technique, Peptide
- Synthesis Techniques, Peptide
- Technique, Peptide Synthesis
- Techniques, Peptide Synthesis
- Peptide Synthesis Methods
- Method, Peptide Synthesis
- Methods, Peptide Synthesis
- Methods of Peptide Synthesis
- Peptide Synthesis Method
- Synthesis Method, Peptide
- Synthesis Methods, Peptide
Inorganic Synthesis- Inorganic Synthesis
- Inorganic Syntheses
- Syntheses, Inorganic
- Synthesis, Inorganic
Organic Synthesis- Organic Synthesis
- Organic Syntheses
- Syntheses, Organic
- Synthesis, Organic
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Below are MeSH descriptors whose meaning is more general than "Chemistry Techniques, Synthetic".
- Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
- Investigative Techniques [E05]
- Technology, Pharmaceutical [E05.916]
- Chemistry Techniques, Synthetic [E05.916.039]
- Biological Sciences [G]
- Chemical Phenomena [G02]
- Organic Chemistry Phenomena [G02.607]
- Organic Chemistry Processes [G02.607.750]
- Chemistry Techniques, Synthetic [G02.607.750.155]
- Technology, Industry, Agriculture [J]
- Technology, Industry, and Agriculture [J01]
- Technology [J01.897]
- Technology, Pharmaceutical [J01.897.836]
- Chemistry Techniques, Synthetic [J01.897.836.249]
Below are MeSH descriptors whose meaning is more specific than "Chemistry Techniques, Synthetic".
This graph shows the total number of publications written about "Chemistry Techniques, Synthetic" by people in UAMS Profiles by year, and whether "Chemistry Techniques, Synthetic" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 0 | 1 | 1 | | 2020 | 0 | 3 | 3 | | 2019 | 0 | 1 | 1 | | 2016 | 0 | 3 | 3 | | 2015 | 0 | 1 | 1 | | 2014 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Chemistry Techniques, Synthetic" by people in Profiles over the past ten years.
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Fulo HF, Shoeib A, Cabanlong CV, Williams AH, Zhan CG, Prather PL, Dudley GB. Synthesis, Molecular Pharmacology, and Structure-Activity Relationships of 3-(Indanoyl)indoles as Selective Cannabinoid Type 2 Receptor Antagonists. J Med Chem. 2021 05 13; 64(9):6381-6396.
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Gujarathi S, Zafar MK, Liu X, Eoff RL, Zheng G. A Facile Semisynthesis and Evaluation of Garcinoic Acid and Its Analogs for the Inhibition of Human DNA Polymerase ?. Molecules. 2020 Dec 11; 25(24).
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Bowroju SK, Mainali N, Ayyadevara S, Penthala NR, Krishnamachari S, Kakraba S, Shmookler Reis RJ, Crooks PA. Design and Synthesis of Novel Hybrid 8-Hydroxy Quinoline-Indole Derivatives as Inhibitors of A? Self-Aggregation and Metal Chelation-Induced A? Aggregation. Molecules. 2020 08 08; 25(16).
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Lakkaniga NR, Gunaganti N, Zhang L, Belachew B, Frett B, Leung YK, Li HY. Pyrrolo[2,3-d]pyrimidine derivatives as inhibitors of RET: Design, synthesis and biological evaluation. Eur J Med Chem. 2020 Nov 15; 206:112691.
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Whitt J, Duke C, Sumlin A, Chambers SA, Alnufaie R, Gilmore D, Fite T, Basnakian AG, Alam MA. Synthesis of Hydrazone Derivatives of 4-[4-Formyl-3-(2-oxochromen-3-yl)pyrazol-1-yl]benzoic acid as Potent Growth Inhibitors of Antibiotic-resistant Staphylococcus aureus and Acinetobacter baumannii. Molecules. 2019 May 29; 24(11).
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Xi JB, Fang YF, Frett B, Zhu ML, Zhu T, Kong YN, Guan FJ, Zhao Y, Zhang XW, Li HY, Ma ML, Hu W. Structure-based design and synthesis of imidazo[1,2-a]pyridine derivatives as novel and potent Nek2 inhibitors with in?vitro and in?vivo antitumor activities. Eur J Med Chem. 2017 Jan 27; 126:1083-1106.
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Zhang X, Tang K, Wang H, Liu Y, Bao B, Fang Y, Zhang X, Lu W. Design, Synthesis, and Biological Evaluation of New Cathepsin B-Sensitive Camptothecin Nanoparticles Equipped with a Novel Multifuctional Linker. Bioconjug Chem. 2016 05 18; 27(5):1267-75.
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Joolakanti SR, Nickell JR, Janganati V, Zheng G, Dwoskin LP, Crooks PA. Lobelane analogues containing 4-hydroxy and 4-(2-fluoroethoxy) aromatic substituents: Potent and selective inhibitors of [(3)H]dopamine uptake at the vesicular monoamine transporter-2. Bioorg Med Chem Lett. 2016 05 15; 26(10):2422-2427.
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Stehouwer JS, Birnbaum MS, Voll RJ, Owens MJ, Plott SJ, Bourke CH, Wassef MA, Kilts CD, Goodman MM. Synthesis, F-18 radiolabeling, and microPET evaluation of 3-(2,4-dichlorophenyl)-N-alkyl-N-fluoroalkyl-2,5-dimethylpyrazolo[1,5-a]pyrimidin-7-amines as ligands of the corticotropin-releasing factor type-1 (CRF1) receptor. Bioorg Med Chem. 2015 Aug 01; 23(15):4286-4302.
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Frett B, McConnell N, Smith CC, Wang Y, Shah NP, Li HY. Computer aided drug discovery of highly ligand efficient, low molecular weight imidazopyridine analogs as FLT3 inhibitors. Eur J Med Chem. 2015 Apr 13; 94:123-31.
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