Medicinal Chemistry Research
基本信息
Medicinal Chemistry Research is a journal for the prompt disclosure of novel experimental achievements in the many facets of drug design, drug discovery, and the elucidation of mechanisms of action of biologically active compounds. Articles are sought which emphasize research in chemical biological relationships, especially on: structure-activity relationships, investigations of biochemical and pharmacological targets of drug action, and correlations of structures with the mode of action of biologically active compounds. Studies will be welcomed that increase our understanding of biochemical interactions between drug molecules, ions, free radicals, and sterically important sections of macromolecular targets. The journal will strive to publish short papers of approximately 8-10 pages within two months of acceptance. A rapid peer-reviewing system will be maintained by the Editors. In addition, reviews and "New Trends" articles will appear at the invitation of the Editors. These articles will be solicited from the leading researchers in all fields of medicinal chemistry. Medicinal Chemistry Research is a Journal dedicated to biologically active compounds including bioactive natural products of plant origin. It publishes original contributions in six major areas: 1. Design, synthesis, and structure-activity relationships of bioactive compounds 2. Docking, molecular modeling, and computational studies of bioactive interactions 3. Characterization of active ingredients of medicinal plants/identification of bioactivity in plant extracts 4. Identification of targets and mechanism of activity of bioactive compounds 5. Chemistry and biochemistry of bioactive natural products of plant origin 6. Critical reviews of the historical, clinical and legal status of medicinal agents, and accounts on topical issues.
CiteScore
| 学科 | 排名 | 百分位 |
|---|---|---|
Pharmacology, Toxicology and PharmaceuticsGeneral Pharmacology, Toxicology and Pharmaceutics |
15 / 80 | 81% |
期刊统计
投稿信息
投稿网址:
https://www.editorialmanager.com/mcre/相关文献
The use of enantiomerically pure ketene dithioacetal bis(sulfoxides) in highly diastereoselective intramolecular nitrone cycloadditions. Application in the total synthesis of the β-amino acid (−)-cispentacin and the first asymmetric synthesis of cis-(3R,4R)-4-amino-pyrrolidine-3-carboxylic acid
Varinder K. Aggarwal, Stephen Roseblade, Rikki Alexander
DOI: 10.1039/B212719A
From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties
DOI: 10.1039/D0QO00723D
Sequence-controlled supramolecular copolymer constructed by self-sorting assembly of multiple noncovalent interactions
Hui Li, Ying Yang, Fenfen Xu, Zhaozhao Duan, Riqiang Li, Herui Wen, Wei Tian
DOI: 10.1039/D0QO01540G
The influence of hydrogen bonding interactions on the C–H bond activation step in class I ribonucleotide reductases
Hendrik Zipse
DOI: 10.1039/B210536P
Recent advances in hydride transfer-involved C(sp3)–H activation reactions
Xiao-De An
DOI: 10.1039/D0QO01502D
(±)-Pinnatifidaones A–D, four pairs of highly modified neolignan enantiomers with a rare spirocyclohexenone skeleton from Crataegus pinnatifida
Rui Guo, Peng Zhao, Xiaoqi Yu, Guodong Yao, Bin Lin, Xiaoxiao Huang, Shaojiang Song
DOI: 10.1039/D0QO01475C
Xanthanoltrimer A–C: three xanthanolide sesquiterpene trimers from the fruits of Xanthium italicum Moretti isolated by HPLC-MS-SPE-NMR
Jiang Fu, Ya-Nan Wang, Shuang-Gang Ma, Li Li, Xiao-Jing Wang, Yong Li, Yun-Bao Liu, Jing Qu, Shi-Shan Yu
DOI: 10.1039/D0QO01541E
Vibrational spectra and conformational isomerism of calixarene building blocks: 2-benzylphenol
Sergei Katsyuba, Alla Chernova, Reinhard Schmutzler
DOI: 10.1039/B211164K
A [15]paracyclophenone and its fluorenone-containing derivatives: syntheses and binding to nerve agent mimics via aryl-CH hydrogen bonding interactions
Peiren Liu, Hongliang Wang, Hong Zeng, Xin Hong, Feihe Huang
DOI: 10.1039/D0QO00456A
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