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Anti-cancer drugs

Elke S. Bergmann-Leitner
- 31 Mar 2005 - 
- Vol. 14, Iss: 11, pp 1048-1048
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This article is published in Current Pharmaceutical Design.The article was published on 2005-03-31. It has received 882 citations till now. The article focuses on the topics: Introductory Journal Article.

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Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases

TL;DR: A novel strategy for cancer drug development by a combination of EGFR/HER2 kinase and HDAC inhibitory activity in one molecule is presented, which is expected to result in a broader activity spectrum and less likelihood of drug resistance in cancer patients.
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Structure–activity studies of Ti(IV) complexes: aqueous stability and cytotoxic properties in colon cancer HT-29 cells

TL;DR: The titanium–maltolato complex had higher levels of cytotoxic activity than any other titanocene complex investigated and may be important in protecting the titanium center from hydrolysis, but this may be achieved by selecting ligands that could result in hydrolytically stable, yet active, complexes.
Journal ArticleDOI

Nanoparticle Ligand Presentation for Targeting Solid Tumors

TL;DR: The types of ligands that have been most often used to target nanoparticles to solid tumors are examined and careful control over ligand presentation on nanoparticles of precise size, shape, and charge will likely play a major role in achieving success.
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Ultra-sensitive quantification of paclitaxel using selective solid-phase extraction in conjunction with reversed-phase capillary liquid chromatography/tandem mass spectrometry.

TL;DR: Selective solid-phase extraction was combined with highly sensitive capillary LC (microLC)-MS/MS analysis to achieve ultra-sensitive quantification of the anti-cancer drug paclitaxel in cancer cells, enabling a high sample loading volume on the microLC column without compromising chromatographic performance and operational robustness.
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Evaluation of DNA-targeted anti-cancer drugs by Raman spectroscopy

TL;DR: In this article, FT-Raman spectroscopy was used to study the interaction of triphenyl phosphonium salts with DNA and showed that compound 5 showed a significant higher inhibitory rate on human cervix cancer cells.
References
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The status of platinum anticancer drugs in the clinic and in clinical trials.

TL;DR: The status of platinum anticancer drugs currently approved for use, those undergoing clinical trials and those discontinued during clinical trials are updated, and the results in the context of where the field will develop over the next decade are discussed.
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Natural products to drugs: natural product derived compounds in clinical trials

TL;DR: Natural product and natural product-derived compounds that are being evaluated in clinical trials or are in registration (as at 31st December 2007) have been reviewed, as well as natural products for which clinical trials have been halted or discontinued since 2005.
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Cellular distribution and functions of P2 receptor subtypes in different systems.

TL;DR: This review is aimed at providing readers with a comprehensive reference article about the distribution and function of P2 receptors in all the organs, tissues, and cells in the body.
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Natural products: an evolving role in future drug discovery.

TL;DR: The present review describes natural products, semi-synthetic NPs and NP-derived compounds that have undergone clinical evaluation or registration from 2005 to 2010 by disease area i.e. infectious, immunological, cardiovascular, neurological, inflammatory and related diseases and oncology.