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Automated medicinal chemistry

Drug Discovery Today, 2006
With the advent of high throughput technologies in biological screening in the 1980s, providing sufficient numbers of small molecules for screening became a bottleneck in the drug discovery process. Combinatorial chemistry was the first attempt by chemists to address this issue. However, since its first applications, combinatorial chemistry has evolved
Marcus, Koppitz, Knut, Eis
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Metallocyclodextrins in Medicinal Chemistry

Future Medicinal Chemistry, 2018
This review focuses on metal complexes of cyclodextrin (CyD) derivatives designed for application as therapeutics or diagnostics. We discuss examples of metalloprotein models (hemoglobin, superoxide dismutase and catalase) based on cyclodextrins. The hydrophobic microenvironment of CyDs stabilizes the Fe(II) porphyrin system that can reversibly bind O2
Valentina Oliveri, Graziella Vecchio
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Medicinal chemistry

Drug Discovery Today: Technologies, 2006
Li-He, Zhang, Kaixian, Chen
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Computational Medicinal Chemistry

Journal of Medicinal Chemistry, 2010
Martin, Stahl, Jürgen, Bajorath
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Perspectives in Medicinal Chemistry:

Current Topics in Medicinal Chemistry, 2015
Guo-Ping, Zhou, Wei-Zhu, Zhong
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